NCPI-FHIR-IMPLEMENTATION-GUIDE\Human Phenotype Ontology - TTL Representation

NCPI FHIR Implementation Guide - Local Development build (v0.2.0). See the Directory of published versions
: Human Phenotype Ontology - TTL Representation

Draft as of 2022-12-09

@prefix fhir: <http://hl7.org/fhir/> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

# - resource -------------------------------------------------------------------

 a fhir:CodeSystem;
  fhir:nodeRole fhir:treeRoot;
  fhir:Resource.id [ fhir:value "hpo"]; # 
  fhir:DomainResource.text [
     fhir:Narrative.status [ fhir:value "generated" ];
     fhir:Narrative.div "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p><b>Properties</b></p><table class=\"grid\"><tr><td><b>Code</b></td><td><b>Type</b></td><td><b>Description</b></td></tr><tr><td>parent</td><td>code</td><td>Parent codes.</td></tr><tr><td>imported</td><td>boolean</td><td>Indicates if the concept is imported from another code system.</td></tr><tr><td>root</td><td>boolean</td><td>Indicates if this concept is a root concept (i.e. Thing is equivalent or a direct parent)</td></tr><tr><td>deprecated</td><td>boolean</td><td>Indicates if this concept is deprecated.</td></tr></table><p><b>Filters</b></p><table class=\"grid\"><tr><td><b>Code</b></td><td><b>Description</b></td><td><b>operator</b></td><td><b>Value</b></td></tr><tr><td>root</td><td/><td>= </td><td>True or false.</td></tr><tr><td>deprecated</td><td/><td>= </td><td>True or false.</td></tr><tr><td>imported</td><td/><td>= </td><td>True or false</td></tr></table><p>This code system <code>http://purl.obolibrary.org/obo/hp.owl</code> defines many codes, of which the following are a subset:</p><table class=\"codes\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td></tr><tr><td style=\"white-space:nowrap\">HP:0000365<a name=\"hpo-HP.580000365\"> </a></td><td>Hearing impairment</td></tr><tr><td style=\"white-space:nowrap\">HP:0002564<a name=\"hpo-HP.580002564\"> </a></td><td>obsolete Malformation of the heart and great vessels</td></tr><tr><td style=\"white-space:nowrap\">HP:0001028<a name=\"hpo-HP.580001028\"> </a></td><td>Hemangioma</td></tr><tr><td style=\"white-space:nowrap\">HP:0000476<a name=\"hpo-HP.580000476\"> </a></td><td>Cystic hygroma</td></tr><tr><td style=\"white-space:nowrap\">HP:0000568<a name=\"hpo-HP.580000568\"> </a></td><td>Microphthalmia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000518<a name=\"hpo-HP.580000518\"> </a></td><td>Cataract</td></tr><tr><td style=\"white-space:nowrap\">HP:0000612<a name=\"hpo-HP.580000612\"> </a></td><td>Iris coloboma</td></tr><tr><td style=\"white-space:nowrap\">HP:0000567<a name=\"hpo-HP.580000567\"> </a></td><td>Chorioretinal coloboma</td></tr><tr><td style=\"white-space:nowrap\">HP:0000316<a name=\"hpo-HP.580000316\"> </a></td><td>Hypertelorism</td></tr><tr><td style=\"white-space:nowrap\">HP:0000482<a name=\"hpo-HP.580000482\"> </a></td><td>Microcornea</td></tr><tr><td style=\"white-space:nowrap\">HP:0000588<a name=\"hpo-HP.580000588\"> </a></td><td>Optic nerve coloboma</td></tr><tr><td style=\"white-space:nowrap\">HP:0004426<a name=\"hpo-HP.580004426\"> </a></td><td>Abnormality of the cheek</td></tr><tr><td style=\"white-space:nowrap\">HP:0009125<a name=\"hpo-HP.580009125\"> </a></td><td>Lipodystrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0002023<a name=\"hpo-HP.580002023\"> </a></td><td>Anal atresia</td></tr><tr><td style=\"white-space:nowrap\">HP:0003468<a name=\"hpo-HP.580003468\"> </a></td><td>Abnormal vertebral morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0000545<a name=\"hpo-HP.580000545\"> </a></td><td>Myopia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000122<a name=\"hpo-HP.580000122\"> </a></td><td>Unilateral renal agenesis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002143<a name=\"hpo-HP.580002143\"> </a></td><td>Abnormality of the spinal cord</td></tr><tr><td style=\"white-space:nowrap\">HP:0003508<a name=\"hpo-HP.580003508\"> </a></td><td>Proportionate short stature</td></tr><tr><td style=\"white-space:nowrap\">HP:0000271<a name=\"hpo-HP.580000271\"> </a></td><td>Abnormality of the face</td></tr><tr><td style=\"white-space:nowrap\">HP:0000637<a name=\"hpo-HP.580000637\"> </a></td><td>Long palpebral fissure</td></tr><tr><td style=\"white-space:nowrap\">HP:0000492<a name=\"hpo-HP.580000492\"> </a></td><td>Abnormal eyelid morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0000389<a name=\"hpo-HP.580000389\"> </a></td><td>Chronic otitis media</td></tr><tr><td style=\"white-space:nowrap\">HP:0000400<a name=\"hpo-HP.580000400\"> </a></td><td>Macrotia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000405<a name=\"hpo-HP.580000405\"> </a></td><td>Conductive hearing impairment</td></tr><tr><td style=\"white-space:nowrap\">HP:0012712<a name=\"hpo-HP.580012712\"> </a></td><td>Mild hearing impairment</td></tr><tr><td style=\"white-space:nowrap\">HP:0005280<a name=\"hpo-HP.580005280\"> </a></td><td>Depressed nasal bridge</td></tr><tr><td style=\"white-space:nowrap\">HP:0000431<a name=\"hpo-HP.580000431\"> </a></td><td>Wide nasal bridge</td></tr><tr><td style=\"white-space:nowrap\">HP:0000319<a name=\"hpo-HP.580000319\"> </a></td><td>Smooth philtrum</td></tr><tr><td style=\"white-space:nowrap\">HP:0000175<a name=\"hpo-HP.580000175\"> </a></td><td>Cleft palate</td></tr><tr><td style=\"white-space:nowrap\">HP:0001611<a name=\"hpo-HP.580001611\"> </a></td><td>Nasal speech</td></tr><tr><td style=\"white-space:nowrap\">HP:0002099<a name=\"hpo-HP.580002099\"> </a></td><td>Asthma</td></tr><tr><td style=\"white-space:nowrap\">HP:0001397<a name=\"hpo-HP.580001397\"> </a></td><td>Hepatic steatosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001081<a name=\"hpo-HP.580001081\"> </a></td><td>Cholelithiasis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002650<a name=\"hpo-HP.580002650\"> </a></td><td>Scoliosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001212<a name=\"hpo-HP.580001212\"> </a></td><td>Prominent fingertip pads</td></tr><tr><td style=\"white-space:nowrap\">HP:0001328<a name=\"hpo-HP.580001328\"> </a></td><td>Specific learning disability</td></tr><tr><td style=\"white-space:nowrap\">HP:0000824<a name=\"hpo-HP.580000824\"> </a></td><td>Growth hormone deficiency</td></tr><tr><td style=\"white-space:nowrap\">HP:0002607<a name=\"hpo-HP.580002607\"> </a></td><td>Bowel incontinence</td></tr><tr><td style=\"white-space:nowrap\">HP:0100731<a name=\"hpo-HP.580100731\"> </a></td><td>Transverse facial cleft</td></tr><tr><td style=\"white-space:nowrap\">HP:0000528<a name=\"hpo-HP.580000528\"> </a></td><td>Anophthalmia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000601<a name=\"hpo-HP.580000601\"> </a></td><td>Hypotelorism</td></tr><tr><td style=\"white-space:nowrap\">HP:0000369<a name=\"hpo-HP.580000369\"> </a></td><td>Low-set ears</td></tr><tr><td style=\"white-space:nowrap\">HP:0001274<a name=\"hpo-HP.580001274\"> </a></td><td>Agenesis of corpus callosum</td></tr><tr><td style=\"white-space:nowrap\">HP:0002084<a name=\"hpo-HP.580002084\"> </a></td><td>Encephalocele</td></tr><tr><td style=\"white-space:nowrap\">HP:0007033<a name=\"hpo-HP.580007033\"> </a></td><td>Cerebellar dysplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0100336<a name=\"hpo-HP.580100336\"> </a></td><td>Bilateral cleft lip</td></tr><tr><td style=\"white-space:nowrap\">HP:0100337<a name=\"hpo-HP.580100337\"> </a></td><td>Bilateral cleft palate</td></tr><tr><td style=\"white-space:nowrap\">HP:0001511<a name=\"hpo-HP.580001511\"> </a></td><td>Intrauterine growth retardation</td></tr><tr><td style=\"white-space:nowrap\">HP:0011451<a name=\"hpo-HP.580011451\"> </a></td><td>Congenital microcephaly</td></tr><tr><td style=\"white-space:nowrap\">HP:0000324<a name=\"hpo-HP.580000324\"> </a></td><td>Facial asymmetry</td></tr><tr><td style=\"white-space:nowrap\">HP:0000581<a name=\"hpo-HP.580000581\"> </a></td><td>Blepharophimosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0000508<a name=\"hpo-HP.580000508\"> </a></td><td>Ptosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0008551<a name=\"hpo-HP.580008551\"> </a></td><td>Microtia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001631<a name=\"hpo-HP.580001631\"> </a></td><td>Atrial septal defect</td></tr><tr><td style=\"white-space:nowrap\">HP:0000085<a name=\"hpo-HP.580000085\"> </a></td><td>Horseshoe kidney</td></tr><tr><td style=\"white-space:nowrap\">HP:0011927<a name=\"hpo-HP.580011927\"> </a></td><td>Short digit</td></tr><tr><td style=\"white-space:nowrap\">HP:0001156<a name=\"hpo-HP.580001156\"> </a></td><td>Brachydactyly</td></tr><tr><td style=\"white-space:nowrap\">HP:0002066<a name=\"hpo-HP.580002066\"> </a></td><td>Gait ataxia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001250<a name=\"hpo-HP.580001250\"> </a></td><td>Seizure</td></tr><tr><td style=\"white-space:nowrap\">HP:0001263<a name=\"hpo-HP.580001263\"> </a></td><td>Global developmental delay</td></tr><tr><td style=\"white-space:nowrap\">HP:0001562<a name=\"hpo-HP.580001562\"> </a></td><td>Oligohydramnios</td></tr><tr><td style=\"white-space:nowrap\">HP:0001195<a name=\"hpo-HP.580001195\"> </a></td><td>Single umbilical artery</td></tr><tr><td style=\"white-space:nowrap\">HP:0006349<a name=\"hpo-HP.580006349\"> </a></td><td>Agenesis of permanent teeth</td></tr><tr><td style=\"white-space:nowrap\">HP:0000668<a name=\"hpo-HP.580000668\"> </a></td><td>Hypodontia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000677<a name=\"hpo-HP.580000677\"> </a></td><td>Oligodontia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001252<a name=\"hpo-HP.580001252\"> </a></td><td>Muscular hypotonia</td></tr><tr><td style=\"white-space:nowrap\">HP:0003429<a name=\"hpo-HP.580003429\"> </a></td><td>CNS hypomyelination</td></tr><tr><td style=\"white-space:nowrap\">HP:0010864<a name=\"hpo-HP.580010864\"> </a></td><td>Intellectual disability, severe</td></tr><tr><td style=\"white-space:nowrap\">HP:0004325<a name=\"hpo-HP.580004325\"> </a></td><td>Decreased body weight</td></tr><tr><td style=\"white-space:nowrap\">HP:0000666<a name=\"hpo-HP.580000666\"> </a></td><td>Horizontal nystagmus</td></tr><tr><td style=\"white-space:nowrap\">HP:0000218<a name=\"hpo-HP.580000218\"> </a></td><td>High palate</td></tr><tr><td style=\"white-space:nowrap\">HP:0010809<a name=\"hpo-HP.580010809\"> </a></td><td>Broad uvula</td></tr><tr><td style=\"white-space:nowrap\">HP:0000767<a name=\"hpo-HP.580000767\"> </a></td><td>Pectus excavatum</td></tr><tr><td style=\"white-space:nowrap\">HP:0003691<a name=\"hpo-HP.580003691\"> </a></td><td>Scapular winging</td></tr><tr><td style=\"white-space:nowrap\">HP:0002616<a name=\"hpo-HP.580002616\"> </a></td><td>Aortic root aneurysm</td></tr><tr><td style=\"white-space:nowrap\">HP:0001601<a name=\"hpo-HP.580001601\"> </a></td><td>Laryngomalacia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002021<a name=\"hpo-HP.580002021\"> </a></td><td>Pyloric stenosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001388<a name=\"hpo-HP.580001388\"> </a></td><td>Joint laxity</td></tr><tr><td style=\"white-space:nowrap\">HP:0001187<a name=\"hpo-HP.580001187\"> </a></td><td>Hyperextensibility of the finger joints</td></tr><tr><td style=\"white-space:nowrap\">HP:0000741<a name=\"hpo-HP.580000741\"> </a></td><td>Apathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0000817<a name=\"hpo-HP.580000817\"> </a></td><td>Poor eye contact</td></tr><tr><td style=\"white-space:nowrap\">HP:0000821<a name=\"hpo-HP.580000821\"> </a></td><td>Hypothyroidism</td></tr><tr><td style=\"white-space:nowrap\">HP:0000002<a name=\"hpo-HP.580000002\"> </a></td><td>Abnormality of body height</td></tr><tr><td style=\"white-space:nowrap\">HP:0000079<a name=\"hpo-HP.580000079\"> </a></td><td>Abnormality of the urinary system</td></tr><tr><td style=\"white-space:nowrap\">HP:0000164<a name=\"hpo-HP.580000164\"> </a></td><td>Abnormality of the dentition</td></tr><tr><td style=\"white-space:nowrap\">HP:0000364<a name=\"hpo-HP.580000364\"> </a></td><td>Hearing abnormality</td></tr><tr><td style=\"white-space:nowrap\">HP:0000366<a name=\"hpo-HP.580000366\"> </a></td><td>Abnormality of the nose</td></tr><tr><td style=\"white-space:nowrap\">HP:0000464<a name=\"hpo-HP.580000464\"> </a></td><td>Abnormality of the neck</td></tr><tr><td style=\"white-space:nowrap\">HP:0000707<a name=\"hpo-HP.580000707\"> </a></td><td>Abnormality of the nervous system</td></tr><tr><td style=\"white-space:nowrap\">HP:0000708<a name=\"hpo-HP.580000708\"> </a></td><td>Behavioral abnormality</td></tr><tr><td style=\"white-space:nowrap\">HP:0000769<a name=\"hpo-HP.580000769\"> </a></td><td>Abnormality of the breast</td></tr><tr><td style=\"white-space:nowrap\">HP:0000772<a name=\"hpo-HP.580000772\"> </a></td><td>Abnormality of the ribs</td></tr><tr><td style=\"white-space:nowrap\">HP:0000775<a name=\"hpo-HP.580000775\"> </a></td><td>Abnormality of the diaphragm</td></tr><tr><td style=\"white-space:nowrap\">HP:0000889<a name=\"hpo-HP.580000889\"> </a></td><td>Abnormality of the clavicle</td></tr><tr><td style=\"white-space:nowrap\">HP:0000925<a name=\"hpo-HP.580000925\"> </a></td><td>Abnormality of the vertebral column</td></tr><tr><td style=\"white-space:nowrap\">HP:0001080<a name=\"hpo-HP.580001080\"> </a></td><td>Biliary tract abnormality</td></tr><tr><td style=\"white-space:nowrap\">HP:0001392<a name=\"hpo-HP.580001392\"> </a></td><td>Abnormality of the liver</td></tr><tr><td style=\"white-space:nowrap\">HP:0001438<a name=\"hpo-HP.580001438\"> </a></td><td>Abnormal abdomen morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0001608<a name=\"hpo-HP.580001608\"> </a></td><td>Abnormality of the voice</td></tr><tr><td style=\"white-space:nowrap\">HP:0001627<a name=\"hpo-HP.580001627\"> </a></td><td>Abnormal heart morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0001732<a name=\"hpo-HP.580001732\"> </a></td><td>Abnormality of the pancreas</td></tr><tr><td style=\"white-space:nowrap\">HP:0001739<a name=\"hpo-HP.580001739\"> </a></td><td>Abnormality of the nasopharynx</td></tr><tr><td style=\"white-space:nowrap\">HP:0001743<a name=\"hpo-HP.580001743\"> </a></td><td>Abnormality of the spleen</td></tr><tr><td style=\"white-space:nowrap\">HP:0001760<a name=\"hpo-HP.580001760\"> </a></td><td>Abnormal foot morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0001871<a name=\"hpo-HP.580001871\"> </a></td><td>Abnormality of blood and blood-forming tissues</td></tr><tr><td style=\"white-space:nowrap\">HP:0002031<a name=\"hpo-HP.580002031\"> </a></td><td>Abnormal esophagus morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0002244<a name=\"hpo-HP.580002244\"> </a></td><td>Abnormality of the small intestine</td></tr><tr><td style=\"white-space:nowrap\">HP:0002246<a name=\"hpo-HP.580002246\"> </a></td><td>Abnormality of the duodenum</td></tr><tr><td style=\"white-space:nowrap\">HP:0002250<a name=\"hpo-HP.580002250\"> </a></td><td>Abnormal large intestine morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0002644<a name=\"hpo-HP.580002644\"> </a></td><td>Abnormality of pelvic girdle bone morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0002664<a name=\"hpo-HP.580002664\"> </a></td><td>Neoplasm</td></tr><tr><td style=\"white-space:nowrap\">HP:0002715<a name=\"hpo-HP.580002715\"> </a></td><td>Abnormality of the immune system</td></tr><tr><td style=\"white-space:nowrap\">HP:0002814<a name=\"hpo-HP.580002814\"> </a></td><td>Abnormality of the lower limb</td></tr><tr><td style=\"white-space:nowrap\">HP:0002817<a name=\"hpo-HP.580002817\"> </a></td><td>Abnormality of the upper limb</td></tr><tr><td style=\"white-space:nowrap\">HP:0005483<a name=\"hpo-HP.580005483\"> </a></td><td>Abnormal epiglottis morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0008777<a name=\"hpo-HP.580008777\"> </a></td><td>Abnormal vocal cord morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0011844<a name=\"hpo-HP.580011844\"> </a></td><td>Abnormal appendicular skeleton morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0012732<a name=\"hpo-HP.580012732\"> </a></td><td>Anorectal anomaly</td></tr><tr><td style=\"white-space:nowrap\">HP:0001508<a name=\"hpo-HP.580001508\"> </a></td><td>Failure to thrive</td></tr><tr><td style=\"white-space:nowrap\">HP:0002902<a name=\"hpo-HP.580002902\"> </a></td><td>Hyponatremia</td></tr><tr><td style=\"white-space:nowrap\">HP:0012236<a name=\"hpo-HP.580012236\"> </a></td><td>Elevated sweat chloride</td></tr><tr><td style=\"white-space:nowrap\">HP:0000347<a name=\"hpo-HP.580000347\"> </a></td><td>Micrognathia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000926<a name=\"hpo-HP.580000926\"> </a></td><td>Platyspondyly</td></tr><tr><td style=\"white-space:nowrap\">HP:0001371<a name=\"hpo-HP.580001371\"> </a></td><td>Flexion contracture</td></tr><tr><td style=\"white-space:nowrap\">HP:0001875<a name=\"hpo-HP.580001875\"> </a></td><td>Neutropenia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001888<a name=\"hpo-HP.580001888\"> </a></td><td>Lymphopenia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002857<a name=\"hpo-HP.580002857\"> </a></td><td>Genu valgum</td></tr><tr><td style=\"white-space:nowrap\">HP:0002986<a name=\"hpo-HP.580002986\"> </a></td><td>Radial bowing</td></tr><tr><td style=\"white-space:nowrap\">HP:0003015<a name=\"hpo-HP.580003015\"> </a></td><td>Flared metaphysis</td></tr><tr><td style=\"white-space:nowrap\">HP:0003025<a name=\"hpo-HP.580003025\"> </a></td><td>Metaphyseal irregularity</td></tr><tr><td style=\"white-space:nowrap\">HP:0003097<a name=\"hpo-HP.580003097\"> </a></td><td>Short femur</td></tr><tr><td style=\"white-space:nowrap\">HP:0003300<a name=\"hpo-HP.580003300\"> </a></td><td>Ovoid vertebral bodies</td></tr><tr><td style=\"white-space:nowrap\">HP:0003307<a name=\"hpo-HP.580003307\"> </a></td><td>Hyperlordosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0004209<a name=\"hpo-HP.580004209\"> </a></td><td>Clinodactyly of the 5th finger</td></tr><tr><td style=\"white-space:nowrap\">HP:0004322<a name=\"hpo-HP.580004322\"> </a></td><td>Short stature</td></tr><tr><td style=\"white-space:nowrap\">HP:0005792<a name=\"hpo-HP.580005792\"> </a></td><td>Short humerus</td></tr><tr><td style=\"white-space:nowrap\">HP:0006248<a name=\"hpo-HP.580006248\"> </a></td><td>Limited wrist movement</td></tr><tr><td style=\"white-space:nowrap\">HP:0000944<a name=\"hpo-HP.580000944\"> </a></td><td>Abnormality of the metaphysis</td></tr><tr><td style=\"white-space:nowrap\">HP:0011921<a name=\"hpo-HP.580011921\"> </a></td><td>Exudative pleural effusion</td></tr><tr><td style=\"white-space:nowrap\">HP:0003043<a name=\"hpo-HP.580003043\"> </a></td><td>Abnormality of the shoulder</td></tr><tr><td style=\"white-space:nowrap\">HP:0000290<a name=\"hpo-HP.580000290\"> </a></td><td>Abnormality of the forehead</td></tr><tr><td style=\"white-space:nowrap\">HP:0005288<a name=\"hpo-HP.580005288\"> </a></td><td>Abnormality of the nares</td></tr><tr><td style=\"white-space:nowrap\">HP:0000234<a name=\"hpo-HP.580000234\"> </a></td><td>Abnormality of the head</td></tr><tr><td style=\"white-space:nowrap\">HP:0004323<a name=\"hpo-HP.580004323\"> </a></td><td>Abnormality of body weight</td></tr><tr><td style=\"white-space:nowrap\">HP:0000483<a name=\"hpo-HP.580000483\"> </a></td><td>Astigmatism</td></tr><tr><td style=\"white-space:nowrap\">HP:0011003<a name=\"hpo-HP.580011003\"> </a></td><td>High myopia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000470<a name=\"hpo-HP.580000470\"> </a></td><td>Short neck</td></tr><tr><td style=\"white-space:nowrap\">HP:0030044<a name=\"hpo-HP.580030044\"> </a></td><td>Flexion contracture of digit</td></tr><tr><td style=\"white-space:nowrap\">HP:0100871<a name=\"hpo-HP.580100871\"> </a></td><td>Abnormality of the palm</td></tr><tr><td style=\"white-space:nowrap\">HP:0004334<a name=\"hpo-HP.580004334\"> </a></td><td>Dermal atrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0001845<a name=\"hpo-HP.580001845\"> </a></td><td>Overlapping toe</td></tr><tr><td style=\"white-space:nowrap\">HP:0000496<a name=\"hpo-HP.580000496\"> </a></td><td>Abnormality of eye movement</td></tr><tr><td style=\"white-space:nowrap\">HP:0001780<a name=\"hpo-HP.580001780\"> </a></td><td>Abnormality of toe</td></tr><tr><td style=\"white-space:nowrap\">HP:0001626<a name=\"hpo-HP.580001626\"> </a></td><td>Abnormality of the cardiovascular system</td></tr><tr><td style=\"white-space:nowrap\">HP:0002086<a name=\"hpo-HP.580002086\"> </a></td><td>Abnormality of the respiratory system</td></tr><tr><td style=\"white-space:nowrap\">HP:0000818<a name=\"hpo-HP.580000818\"> </a></td><td>Abnormality of the endocrine system</td></tr><tr><td style=\"white-space:nowrap\">HP:0012372<a name=\"hpo-HP.580012372\"> </a></td><td>Abnormal eye morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0009473<a name=\"hpo-HP.580009473\"> </a></td><td>Joint contracture of the hand</td></tr><tr><td style=\"white-space:nowrap\">HP:0003199<a name=\"hpo-HP.580003199\"> </a></td><td>Decreased muscle mass</td></tr><tr><td style=\"white-space:nowrap\">HP:0003202<a name=\"hpo-HP.580003202\"> </a></td><td>Skeletal muscle atrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0003551<a name=\"hpo-HP.580003551\"> </a></td><td>Difficulty climbing stairs</td></tr><tr><td style=\"white-space:nowrap\">HP:0002355<a name=\"hpo-HP.580002355\"> </a></td><td>Difficulty walking</td></tr><tr><td style=\"white-space:nowrap\">HP:0003546<a name=\"hpo-HP.580003546\"> </a></td><td>Exercise intolerance</td></tr><tr><td style=\"white-space:nowrap\">HP:0003325<a name=\"hpo-HP.580003325\"> </a></td><td>Limb-girdle muscle weakness</td></tr><tr><td style=\"white-space:nowrap\">HP:0003701<a name=\"hpo-HP.580003701\"> </a></td><td>Proximal muscle weakness</td></tr><tr><td style=\"white-space:nowrap\">HP:0003547<a name=\"hpo-HP.580003547\"> </a></td><td>Shoulder girdle muscle weakness</td></tr><tr><td style=\"white-space:nowrap\">HP:0007340<a name=\"hpo-HP.580007340\"> </a></td><td>Lower limb muscle weakness</td></tr><tr><td style=\"white-space:nowrap\">HP:0002168<a name=\"hpo-HP.580002168\"> </a></td><td>Scanning speech</td></tr><tr><td style=\"white-space:nowrap\">HP:0001265<a name=\"hpo-HP.580001265\"> </a></td><td>Hyporeflexia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001284<a name=\"hpo-HP.580001284\"> </a></td><td>Areflexia</td></tr><tr><td style=\"white-space:nowrap\">HP:0003477<a name=\"hpo-HP.580003477\"> </a></td><td>Peripheral axonal neuropathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0000924<a name=\"hpo-HP.580000924\"> </a></td><td>Abnormality of the skeletal system</td></tr><tr><td style=\"white-space:nowrap\">HP:0001291<a name=\"hpo-HP.580001291\"> </a></td><td>Abnormal cranial nerve morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0003687<a name=\"hpo-HP.580003687\"> </a></td><td>Centrally nucleated skeletal muscle fibers</td></tr><tr><td style=\"white-space:nowrap\">HP:0001324<a name=\"hpo-HP.580001324\"> </a></td><td>Muscle weakness</td></tr><tr><td style=\"white-space:nowrap\">HP:0002515<a name=\"hpo-HP.580002515\"> </a></td><td>Waddling gait</td></tr><tr><td style=\"white-space:nowrap\">HP:0100280<a name=\"hpo-HP.580100280\"> </a></td><td>Crohn's disease</td></tr><tr><td style=\"white-space:nowrap\">HP:0002631<a name=\"hpo-HP.580002631\"> </a></td><td>obsolete Dilatation of ascending aorta</td></tr><tr><td style=\"white-space:nowrap\">HP:0100026<a name=\"hpo-HP.580100026\"> </a></td><td>Arteriovenous malformation</td></tr><tr><td style=\"white-space:nowrap\">HP:0002637<a name=\"hpo-HP.580002637\"> </a></td><td>Cerebral ischemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002619<a name=\"hpo-HP.580002619\"> </a></td><td>Varicose veins</td></tr><tr><td style=\"white-space:nowrap\">HP:0001159<a name=\"hpo-HP.580001159\"> </a></td><td>Syndactyly</td></tr><tr><td style=\"white-space:nowrap\">HP:0002069<a name=\"hpo-HP.580002069\"> </a></td><td>Bilateral tonic-clonic seizure</td></tr><tr><td style=\"white-space:nowrap\">HP:0000977<a name=\"hpo-HP.580000977\"> </a></td><td>Soft skin</td></tr><tr><td style=\"white-space:nowrap\">HP:0010648<a name=\"hpo-HP.580010648\"> </a></td><td>Dermal translucency</td></tr><tr><td style=\"white-space:nowrap\">HP:0000978<a name=\"hpo-HP.580000978\"> </a></td><td>Bruising susceptibility</td></tr><tr><td style=\"white-space:nowrap\">HP:0001956<a name=\"hpo-HP.580001956\"> </a></td><td>Truncal obesity</td></tr><tr><td style=\"white-space:nowrap\">HP:0000189<a name=\"hpo-HP.580000189\"> </a></td><td>Narrow palate</td></tr><tr><td style=\"white-space:nowrap\">HP:0000678<a name=\"hpo-HP.580000678\"> </a></td><td>Dental crowding</td></tr><tr><td style=\"white-space:nowrap\">HP:0002870<a name=\"hpo-HP.580002870\"> </a></td><td>Obstructive sleep apnea</td></tr><tr><td style=\"white-space:nowrap\">HP:0001763<a name=\"hpo-HP.580001763\"> </a></td><td>Pes planus</td></tr><tr><td style=\"white-space:nowrap\">HP:0000782<a name=\"hpo-HP.580000782\"> </a></td><td>Abnormality of the scapula</td></tr><tr><td style=\"white-space:nowrap\">HP:0001600<a name=\"hpo-HP.580001600\"> </a></td><td>Abnormality of the larynx</td></tr><tr><td style=\"white-space:nowrap\">HP:0002088<a name=\"hpo-HP.580002088\"> </a></td><td>Abnormal lung morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0011407<a name=\"hpo-HP.580011407\"> </a></td><td>Proportionate tall stature</td></tr><tr><td style=\"white-space:nowrap\">HP:0000541<a name=\"hpo-HP.580000541\"> </a></td><td>Retinal detachment</td></tr><tr><td style=\"white-space:nowrap\">HP:0001373<a name=\"hpo-HP.580001373\"> </a></td><td>Joint dislocation</td></tr><tr><td style=\"white-space:nowrap\">HP:0000938<a name=\"hpo-HP.580000938\"> </a></td><td>Osteopenia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002942<a name=\"hpo-HP.580002942\"> </a></td><td>Thoracic kyphosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001840<a name=\"hpo-HP.580001840\"> </a></td><td>Metatarsus adductus</td></tr><tr><td style=\"white-space:nowrap\">HP:0001844<a name=\"hpo-HP.580001844\"> </a></td><td>Abnormality of the hallux</td></tr><tr><td style=\"white-space:nowrap\">HP:0001765<a name=\"hpo-HP.580001765\"> </a></td><td>Hammertoe</td></tr><tr><td style=\"white-space:nowrap\">HP:0000606<a name=\"hpo-HP.580000606\"> </a></td><td>Abnormality of the periorbital region</td></tr><tr><td style=\"white-space:nowrap\">HP:0002757<a name=\"hpo-HP.580002757\"> </a></td><td>Recurrent fractures</td></tr><tr><td style=\"white-space:nowrap\">HP:0000647<a name=\"hpo-HP.580000647\"> </a></td><td>Sclerocornea</td></tr><tr><td style=\"white-space:nowrap\">HP:0001166<a name=\"hpo-HP.580001166\"> </a></td><td>Arachnodactyly</td></tr><tr><td style=\"white-space:nowrap\">HP:0005490<a name=\"hpo-HP.580005490\"> </a></td><td>Postnatal macrocephaly</td></tr><tr><td style=\"white-space:nowrap\">HP:0011363<a name=\"hpo-HP.580011363\"> </a></td><td>Abnormality of hair growth rate</td></tr><tr><td style=\"white-space:nowrap\">HP:0000276<a name=\"hpo-HP.580000276\"> </a></td><td>Long face</td></tr><tr><td style=\"white-space:nowrap\">HP:0000275<a name=\"hpo-HP.580000275\"> </a></td><td>Narrow face</td></tr><tr><td style=\"white-space:nowrap\">HP:0000337<a name=\"hpo-HP.580000337\"> </a></td><td>Broad forehead</td></tr><tr><td style=\"white-space:nowrap\">HP:0002267<a name=\"hpo-HP.580002267\"> </a></td><td>Exaggerated startle response</td></tr><tr><td style=\"white-space:nowrap\">HP:0002187<a name=\"hpo-HP.580002187\"> </a></td><td>Intellectual disability, profound</td></tr><tr><td style=\"white-space:nowrap\">HP:0000728<a name=\"hpo-HP.580000728\"> </a></td><td>Impaired ability to form peer relationships</td></tr><tr><td style=\"white-space:nowrap\">HP:0000733<a name=\"hpo-HP.580000733\"> </a></td><td>Stereotypy</td></tr><tr><td style=\"white-space:nowrap\">HP:0000739<a name=\"hpo-HP.580000739\"> </a></td><td>Anxiety</td></tr><tr><td style=\"white-space:nowrap\">HP:0000929<a name=\"hpo-HP.580000929\"> </a></td><td>Abnormal skull morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0001965<a name=\"hpo-HP.580001965\"> </a></td><td>Abnormal scalp morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0100538<a name=\"hpo-HP.580100538\"> </a></td><td>Abnormality of the supraorbital ridges</td></tr><tr><td style=\"white-space:nowrap\">HP:0000309<a name=\"hpo-HP.580000309\"> </a></td><td>Abnormality of the midface</td></tr><tr><td style=\"white-space:nowrap\">HP:0000277<a name=\"hpo-HP.580000277\"> </a></td><td>Abnormality of the mandible</td></tr><tr><td style=\"white-space:nowrap\">HP:0000765<a name=\"hpo-HP.580000765\"> </a></td><td>Abnormality of the thorax</td></tr><tr><td style=\"white-space:nowrap\">HP:0100008<a name=\"hpo-HP.580100008\"> </a></td><td>Schwannoma</td></tr><tr><td style=\"white-space:nowrap\">HP:0030038<a name=\"hpo-HP.580030038\"> </a></td><td>Enchondroma</td></tr><tr><td style=\"white-space:nowrap\">HP:0100777<a name=\"hpo-HP.580100777\"> </a></td><td>Exostoses</td></tr><tr><td style=\"white-space:nowrap\">HP:0011663<a name=\"hpo-HP.580011663\"> </a></td><td>Right ventricular cardiomyopathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0011675<a name=\"hpo-HP.580011675\"> </a></td><td>Arrhythmia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001962<a name=\"hpo-HP.580001962\"> </a></td><td>Palpitations</td></tr><tr><td style=\"white-space:nowrap\">HP:0001279<a name=\"hpo-HP.580001279\"> </a></td><td>Syncope</td></tr><tr><td style=\"white-space:nowrap\">HP:0004756<a name=\"hpo-HP.580004756\"> </a></td><td>Ventricular tachycardia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000252<a name=\"hpo-HP.580000252\"> </a></td><td>Microcephaly</td></tr><tr><td style=\"white-space:nowrap\">HP:0000303<a name=\"hpo-HP.580000303\"> </a></td><td>Mandibular prognathia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000664<a name=\"hpo-HP.580000664\"> </a></td><td>Synophrys</td></tr><tr><td style=\"white-space:nowrap\">HP:0001609<a name=\"hpo-HP.580001609\"> </a></td><td>Hoarse voice</td></tr><tr><td style=\"white-space:nowrap\">HP:0002558<a name=\"hpo-HP.580002558\"> </a></td><td>Supernumerary nipple</td></tr><tr><td style=\"white-space:nowrap\">HP:0001634<a name=\"hpo-HP.580001634\"> </a></td><td>Mitral valve prolapse</td></tr><tr><td style=\"white-space:nowrap\">HP:0000028<a name=\"hpo-HP.580000028\"> </a></td><td>Cryptorchidism</td></tr><tr><td style=\"white-space:nowrap\">HP:0000973<a name=\"hpo-HP.580000973\"> </a></td><td>Cutis laxa</td></tr><tr><td style=\"white-space:nowrap\">HP:0001518<a name=\"hpo-HP.580001518\"> </a></td><td>Small for gestational age</td></tr><tr><td style=\"white-space:nowrap\">HP:0000527<a name=\"hpo-HP.580000527\"> </a></td><td>Long eyelashes</td></tr><tr><td style=\"white-space:nowrap\">HP:0002808<a name=\"hpo-HP.580002808\"> </a></td><td>Kyphosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0000248<a name=\"hpo-HP.580000248\"> </a></td><td>Brachycephaly</td></tr><tr><td style=\"white-space:nowrap\">HP:0000505<a name=\"hpo-HP.580000505\"> </a></td><td>Visual impairment</td></tr><tr><td style=\"white-space:nowrap\">HP:0000512<a name=\"hpo-HP.580000512\"> </a></td><td>Abnormal electroretinogram</td></tr><tr><td style=\"white-space:nowrap\">HP:0000517<a name=\"hpo-HP.580000517\"> </a></td><td>Abnormality of the lens</td></tr><tr><td style=\"white-space:nowrap\">HP:0000529<a name=\"hpo-HP.580000529\"> </a></td><td>Progressive visual loss</td></tr><tr><td style=\"white-space:nowrap\">HP:0000586<a name=\"hpo-HP.580000586\"> </a></td><td>Shallow orbits</td></tr><tr><td style=\"white-space:nowrap\">HP:0000603<a name=\"hpo-HP.580000603\"> </a></td><td>Central scotoma</td></tr><tr><td style=\"white-space:nowrap\">HP:0000939<a name=\"hpo-HP.580000939\"> </a></td><td>Osteoporosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001377<a name=\"hpo-HP.580001377\"> </a></td><td>Limited elbow extension</td></tr><tr><td style=\"white-space:nowrap\">HP:0001387<a name=\"hpo-HP.580001387\"> </a></td><td>Joint stiffness</td></tr><tr><td style=\"white-space:nowrap\">HP:0001822<a name=\"hpo-HP.580001822\"> </a></td><td>Hallux valgus</td></tr><tr><td style=\"white-space:nowrap\">HP:0002657<a name=\"hpo-HP.580002657\"> </a></td><td>Spondylometaphyseal dysplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0003026<a name=\"hpo-HP.580003026\"> </a></td><td>Short long bone</td></tr><tr><td style=\"white-space:nowrap\">HP:0006462<a name=\"hpo-HP.580006462\"> </a></td><td>Generalized bone demineralization</td></tr><tr><td style=\"white-space:nowrap\">HP:0008873<a name=\"hpo-HP.580008873\"> </a></td><td>Disproportionate short-limb short stature</td></tr><tr><td style=\"white-space:nowrap\">HP:0008905<a name=\"hpo-HP.580008905\"> </a></td><td>Rhizomelia</td></tr><tr><td style=\"white-space:nowrap\">HP:0008922<a name=\"hpo-HP.580008922\"> </a></td><td>Childhood-onset short-trunk short stature</td></tr><tr><td style=\"white-space:nowrap\">HP:0200020<a name=\"hpo-HP.580200020\"> </a></td><td>Corneal erosion</td></tr><tr><td style=\"white-space:nowrap\">HP:0001172<a name=\"hpo-HP.580001172\"> </a></td><td>Abnormal thumb morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0002286<a name=\"hpo-HP.580002286\"> </a></td><td>Fair hair</td></tr><tr><td style=\"white-space:nowrap\">HP:0010719<a name=\"hpo-HP.580010719\"> </a></td><td>Abnormality of hair texture</td></tr><tr><td style=\"white-space:nowrap\">HP:0010720<a name=\"hpo-HP.580010720\"> </a></td><td>Abnormal hair pattern</td></tr><tr><td style=\"white-space:nowrap\">HP:0001635<a name=\"hpo-HP.580001635\"> </a></td><td>Congestive heart failure</td></tr><tr><td style=\"white-space:nowrap\">HP:0001644<a name=\"hpo-HP.580001644\"> </a></td><td>Dilated cardiomyopathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0001663<a name=\"hpo-HP.580001663\"> </a></td><td>Ventricular fibrillation</td></tr><tr><td style=\"white-space:nowrap\">HP:0011712<a name=\"hpo-HP.580011712\"> </a></td><td>Right bundle branch block</td></tr><tr><td style=\"white-space:nowrap\">HP:0000272<a name=\"hpo-HP.580000272\"> </a></td><td>Malar flattening</td></tr><tr><td style=\"white-space:nowrap\">HP:0000286<a name=\"hpo-HP.580000286\"> </a></td><td>Epicanthus</td></tr><tr><td style=\"white-space:nowrap\">HP:0000322<a name=\"hpo-HP.580000322\"> </a></td><td>Short philtrum</td></tr><tr><td style=\"white-space:nowrap\">HP:0000463<a name=\"hpo-HP.580000463\"> </a></td><td>Anteverted nares</td></tr><tr><td style=\"white-space:nowrap\">HP:0000494<a name=\"hpo-HP.580000494\"> </a></td><td>Downslanted palpebral fissures</td></tr><tr><td style=\"white-space:nowrap\">HP:0000543<a name=\"hpo-HP.580000543\"> </a></td><td>Optic disc pallor</td></tr><tr><td style=\"white-space:nowrap\">HP:0000699<a name=\"hpo-HP.580000699\"> </a></td><td>Diastema</td></tr><tr><td style=\"white-space:nowrap\">HP:0000773<a name=\"hpo-HP.580000773\"> </a></td><td>Short ribs</td></tr><tr><td style=\"white-space:nowrap\">HP:0000887<a name=\"hpo-HP.580000887\"> </a></td><td>Cupped ribs</td></tr><tr><td style=\"white-space:nowrap\">HP:0000946<a name=\"hpo-HP.580000946\"> </a></td><td>Hypoplastic ilia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000954<a name=\"hpo-HP.580000954\"> </a></td><td>Single transverse palmar crease</td></tr><tr><td style=\"white-space:nowrap\">HP:0001182<a name=\"hpo-HP.580001182\"> </a></td><td>Tapered finger</td></tr><tr><td style=\"white-space:nowrap\">HP:0001537<a name=\"hpo-HP.580001537\"> </a></td><td>Umbilical hernia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002007<a name=\"hpo-HP.580002007\"> </a></td><td>Frontal bossing</td></tr><tr><td style=\"white-space:nowrap\">HP:0002980<a name=\"hpo-HP.580002980\"> </a></td><td>Femoral bowing</td></tr><tr><td style=\"white-space:nowrap\">HP:0002982<a name=\"hpo-HP.580002982\"> </a></td><td>Tibial bowing</td></tr><tr><td style=\"white-space:nowrap\">HP:0003021<a name=\"hpo-HP.580003021\"> </a></td><td>Metaphyseal cupping</td></tr><tr><td style=\"white-space:nowrap\">HP:0005011<a name=\"hpo-HP.580005011\"> </a></td><td>Mesomelic arm shortening</td></tr><tr><td style=\"white-space:nowrap\">HP:0008803<a name=\"hpo-HP.580008803\"> </a></td><td>obsolete Narrow sacroiliac notch</td></tr><tr><td style=\"white-space:nowrap\">HP:0009117<a name=\"hpo-HP.580009117\"> </a></td><td>Aplasia/Hypoplasia of the maxilla</td></tr><tr><td style=\"white-space:nowrap\">HP:0011220<a name=\"hpo-HP.580011220\"> </a></td><td>Prominent forehead</td></tr><tr><td style=\"white-space:nowrap\">HP:0012801<a name=\"hpo-HP.580012801\"> </a></td><td>Narrow jaw</td></tr><tr><td style=\"white-space:nowrap\">HP:0000243<a name=\"hpo-HP.580000243\"> </a></td><td>Trigonocephaly</td></tr><tr><td style=\"white-space:nowrap\">HP:0000358<a name=\"hpo-HP.580000358\"> </a></td><td>Posteriorly rotated ears</td></tr><tr><td style=\"white-space:nowrap\">HP:0000411<a name=\"hpo-HP.580000411\"> </a></td><td>Protruding ear</td></tr><tr><td style=\"white-space:nowrap\">HP:0000646<a name=\"hpo-HP.580000646\"> </a></td><td>Amblyopia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002812<a name=\"hpo-HP.580002812\"> </a></td><td>Coxa vara</td></tr><tr><td style=\"white-space:nowrap\">HP:0002970<a name=\"hpo-HP.580002970\"> </a></td><td>Genu varum</td></tr><tr><td style=\"white-space:nowrap\">HP:0012775<a name=\"hpo-HP.580012775\"> </a></td><td>Stellate iris</td></tr><tr><td style=\"white-space:nowrap\">HP:0000278<a name=\"hpo-HP.580000278\"> </a></td><td>Retrognathia</td></tr><tr><td style=\"white-space:nowrap\">HP:0009796<a name=\"hpo-HP.580009796\"> </a></td><td>Branchial cyst</td></tr><tr><td style=\"white-space:nowrap\">HP:0002474<a name=\"hpo-HP.580002474\"> </a></td><td>Expressive language delay</td></tr><tr><td style=\"white-space:nowrap\">HP:0007018<a name=\"hpo-HP.580007018\"> </a></td><td>Attention deficit hyperactivity disorder</td></tr><tr><td style=\"white-space:nowrap\">HP:0003198<a name=\"hpo-HP.580003198\"> </a></td><td>Myopathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0003324<a name=\"hpo-HP.580003324\"> </a></td><td>Generalized muscle weakness</td></tr><tr><td style=\"white-space:nowrap\">HP:0003552<a name=\"hpo-HP.580003552\"> </a></td><td>Muscle stiffness</td></tr><tr><td style=\"white-space:nowrap\">HP:0003554<a name=\"hpo-HP.580003554\"> </a></td><td>Type 2 muscle fiber atrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0003557<a name=\"hpo-HP.580003557\"> </a></td><td>Increased variability in muscle fiber diameter</td></tr><tr><td style=\"white-space:nowrap\">HP:0009025<a name=\"hpo-HP.580009025\"> </a></td><td>Increased connective tissue</td></tr><tr><td style=\"white-space:nowrap\">HP:0003635<a name=\"hpo-HP.580003635\"> </a></td><td>Loss of subcutaneous adipose tissue in limbs</td></tr><tr><td style=\"white-space:nowrap\">HP:0002597<a name=\"hpo-HP.580002597\"> </a></td><td>Abnormality of the vasculature</td></tr><tr><td style=\"white-space:nowrap\">HP:0001649<a name=\"hpo-HP.580001649\"> </a></td><td>Tachycardia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001638<a name=\"hpo-HP.580001638\"> </a></td><td>Cardiomyopathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0001654<a name=\"hpo-HP.580001654\"> </a></td><td>Abnormal heart valve morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0001671<a name=\"hpo-HP.580001671\"> </a></td><td>Abnormal cardiac septum morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0000103<a name=\"hpo-HP.580000103\"> </a></td><td>Polyuria</td></tr><tr><td style=\"white-space:nowrap\">HP:0000114<a name=\"hpo-HP.580000114\"> </a></td><td>Proximal tubulopathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0001878<a name=\"hpo-HP.580001878\"> </a></td><td>Hemolytic anemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001931<a name=\"hpo-HP.580001931\"> </a></td><td>Hypochromic anemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001935<a name=\"hpo-HP.580001935\"> </a></td><td>Microcytic anemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001959<a name=\"hpo-HP.580001959\"> </a></td><td>Polydipsia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001994<a name=\"hpo-HP.580001994\"> </a></td><td>Renal Fanconi syndrome</td></tr><tr><td style=\"white-space:nowrap\">HP:0002134<a name=\"hpo-HP.580002134\"> </a></td><td>Abnormality of the basal ganglia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002188<a name=\"hpo-HP.580002188\"> </a></td><td>Delayed CNS myelination</td></tr><tr><td style=\"white-space:nowrap\">HP:0002908<a name=\"hpo-HP.580002908\"> </a></td><td>Conjugated hyperbilirubinemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0003774<a name=\"hpo-HP.580003774\"> </a></td><td>Stage 5 chronic kidney disease</td></tr><tr><td style=\"white-space:nowrap\">HP:0010700<a name=\"hpo-HP.580010700\"> </a></td><td>obsolete Total cataract</td></tr><tr><td style=\"white-space:nowrap\">HP:0000193<a name=\"hpo-HP.580000193\"> </a></td><td>Bifid uvula</td></tr><tr><td style=\"white-space:nowrap\">HP:0000219<a name=\"hpo-HP.580000219\"> </a></td><td>Thin upper lip vermilion</td></tr><tr><td style=\"white-space:nowrap\">HP:0000426<a name=\"hpo-HP.580000426\"> </a></td><td>Prominent nasal bridge</td></tr><tr><td style=\"white-space:nowrap\">HP:0000452<a name=\"hpo-HP.580000452\"> </a></td><td>Choanal stenosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0000490<a name=\"hpo-HP.580000490\"> </a></td><td>Deeply set eye</td></tr><tr><td style=\"white-space:nowrap\">HP:0000540<a name=\"hpo-HP.580000540\"> </a></td><td>Hypermetropia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000579<a name=\"hpo-HP.580000579\"> </a></td><td>Nasolacrimal duct obstruction</td></tr><tr><td style=\"white-space:nowrap\">HP:0000684<a name=\"hpo-HP.580000684\"> </a></td><td>Delayed eruption of teeth</td></tr><tr><td style=\"white-space:nowrap\">HP:0000960<a name=\"hpo-HP.580000960\"> </a></td><td>Sacral dimple</td></tr><tr><td style=\"white-space:nowrap\">HP:0000998<a name=\"hpo-HP.580000998\"> </a></td><td>Hypertrichosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001643<a name=\"hpo-HP.580001643\"> </a></td><td>Patent ductus arteriosus</td></tr><tr><td style=\"white-space:nowrap\">HP:0010813<a name=\"hpo-HP.580010813\"> </a></td><td>Abnormal number of hair whorls</td></tr><tr><td style=\"white-space:nowrap\">HP:0012384<a name=\"hpo-HP.580012384\"> </a></td><td>Rhinitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0012745<a name=\"hpo-HP.580012745\"> </a></td><td>Short palpebral fissure</td></tr><tr><td style=\"white-space:nowrap\">HP:0000359<a name=\"hpo-HP.580000359\"> </a></td><td>Abnormality of the inner ear</td></tr><tr><td style=\"white-space:nowrap\">HP:0000429<a name=\"hpo-HP.580000429\"> </a></td><td>Abnormality of the nasal alae</td></tr><tr><td style=\"white-space:nowrap\">HP:0000436<a name=\"hpo-HP.580000436\"> </a></td><td>Abnormality of the nasal tip</td></tr><tr><td style=\"white-space:nowrap\">HP:0000499<a name=\"hpo-HP.580000499\"> </a></td><td>Abnormal eyelash morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0000534<a name=\"hpo-HP.580000534\"> </a></td><td>Abnormal eyebrow morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0000951<a name=\"hpo-HP.580000951\"> </a></td><td>Abnormality of the skin</td></tr><tr><td style=\"white-space:nowrap\">HP:0001000<a name=\"hpo-HP.580001000\"> </a></td><td>Abnormality of skin pigmentation</td></tr><tr><td style=\"white-space:nowrap\">HP:0001597<a name=\"hpo-HP.580001597\"> </a></td><td>Abnormality of the nail</td></tr><tr><td style=\"white-space:nowrap\">HP:0006483<a name=\"hpo-HP.580006483\"> </a></td><td>Abnormal number of teeth</td></tr><tr><td style=\"white-space:nowrap\">HP:0009929<a name=\"hpo-HP.580009929\"> </a></td><td>Abnormality of the columella</td></tr><tr><td style=\"white-space:nowrap\">HP:0011119<a name=\"hpo-HP.580011119\"> </a></td><td>Abnormality of the nasal dorsum</td></tr><tr><td style=\"white-space:nowrap\">HP:0012808<a name=\"hpo-HP.580012808\"> </a></td><td>Abnormal nasal base</td></tr><tr><td style=\"white-space:nowrap\">HP:0100490<a name=\"hpo-HP.580100490\"> </a></td><td>Camptodactyly of finger</td></tr><tr><td style=\"white-space:nowrap\">HP:0000964<a name=\"hpo-HP.580000964\"> </a></td><td>Eczema</td></tr><tr><td style=\"white-space:nowrap\">HP:0004442<a name=\"hpo-HP.580004442\"> </a></td><td>Sagittal craniosynostosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0000414<a name=\"hpo-HP.580000414\"> </a></td><td>Bulbous nose</td></tr><tr><td style=\"white-space:nowrap\">HP:0003180<a name=\"hpo-HP.580003180\"> </a></td><td>Flat acetabular roof</td></tr><tr><td style=\"white-space:nowrap\">HP:0000422<a name=\"hpo-HP.580000422\"> </a></td><td>Abnormality of the nasal bridge</td></tr><tr><td style=\"white-space:nowrap\">HP:0000614<a name=\"hpo-HP.580000614\"> </a></td><td>Abnormal nasolacrimal system morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0001167<a name=\"hpo-HP.580001167\"> </a></td><td>Abnormality of finger</td></tr><tr><td style=\"white-space:nowrap\">HP:0001595<a name=\"hpo-HP.580001595\"> </a></td><td>Abnormal hair morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0012373<a name=\"hpo-HP.580012373\"> </a></td><td>Abnormal eye physiology</td></tr><tr><td style=\"white-space:nowrap\">HP:0001655<a name=\"hpo-HP.580001655\"> </a></td><td>Patent foramen ovale</td></tr><tr><td style=\"white-space:nowrap\">HP:0001647<a name=\"hpo-HP.580001647\"> </a></td><td>Bicuspid aortic valve</td></tr><tr><td style=\"white-space:nowrap\">HP:0000574<a name=\"hpo-HP.580000574\"> </a></td><td>Thick eyebrow</td></tr><tr><td style=\"white-space:nowrap\">HP:0001169<a name=\"hpo-HP.580001169\"> </a></td><td>Broad palm</td></tr><tr><td style=\"white-space:nowrap\">HP:0006471<a name=\"hpo-HP.580006471\"> </a></td><td>Fixed elbow flexion</td></tr><tr><td style=\"white-space:nowrap\">HP:0008689<a name=\"hpo-HP.580008689\"> </a></td><td>Bilateral cryptorchidism</td></tr><tr><td style=\"white-space:nowrap\">HP:0011304<a name=\"hpo-HP.580011304\"> </a></td><td>Broad thumb</td></tr><tr><td style=\"white-space:nowrap\">HP:0005110<a name=\"hpo-HP.580005110\"> </a></td><td>Atrial fibrillation</td></tr><tr><td style=\"white-space:nowrap\">HP:0001633<a name=\"hpo-HP.580001633\"> </a></td><td>Abnormal mitral valve morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0001641<a name=\"hpo-HP.580001641\"> </a></td><td>Abnormal pulmonary valve morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0001702<a name=\"hpo-HP.580001702\"> </a></td><td>Abnormal tricuspid valve morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0000012<a name=\"hpo-HP.580000012\"> </a></td><td>Urinary urgency</td></tr><tr><td style=\"white-space:nowrap\">HP:0000020<a name=\"hpo-HP.580000020\"> </a></td><td>Urinary incontinence</td></tr><tr><td style=\"white-space:nowrap\">HP:0000131<a name=\"hpo-HP.580000131\"> </a></td><td>Uterine leiomyoma</td></tr><tr><td style=\"white-space:nowrap\">HP:0000132<a name=\"hpo-HP.580000132\"> </a></td><td>Menorrhagia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000138<a name=\"hpo-HP.580000138\"> </a></td><td>Ovarian cyst</td></tr><tr><td style=\"white-space:nowrap\">HP:0000853<a name=\"hpo-HP.580000853\"> </a></td><td>Goiter</td></tr><tr><td style=\"white-space:nowrap\">HP:0000953<a name=\"hpo-HP.580000953\"> </a></td><td>Hyperpigmentation of the skin</td></tr><tr><td style=\"white-space:nowrap\">HP:0001061<a name=\"hpo-HP.580001061\"> </a></td><td>Acne</td></tr><tr><td style=\"white-space:nowrap\">HP:0002315<a name=\"hpo-HP.580002315\"> </a></td><td>Headache</td></tr><tr><td style=\"white-space:nowrap\">HP:0004324<a name=\"hpo-HP.580004324\"> </a></td><td>Increased body weight</td></tr><tr><td style=\"white-space:nowrap\">HP:0000069<a name=\"hpo-HP.580000069\"> </a></td><td>Abnormality of the ureter</td></tr><tr><td style=\"white-space:nowrap\">HP:0000077<a name=\"hpo-HP.580000077\"> </a></td><td>Abnormality of the kidney</td></tr><tr><td style=\"white-space:nowrap\">HP:0000759<a name=\"hpo-HP.580000759\"> </a></td><td>Abnormal peripheral nervous system morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0008069<a name=\"hpo-HP.580008069\"> </a></td><td>Neoplasm of the skin</td></tr><tr><td style=\"white-space:nowrap\">HP:0011276<a name=\"hpo-HP.580011276\"> </a></td><td>Vascular skin abnormality</td></tr><tr><td style=\"white-space:nowrap\">HP:0000705<a name=\"hpo-HP.580000705\"> </a></td><td>Amelogenesis imperfecta</td></tr><tr><td style=\"white-space:nowrap\">HP:0001256<a name=\"hpo-HP.580001256\"> </a></td><td>Intellectual disability, mild</td></tr><tr><td style=\"white-space:nowrap\">HP:0000325<a name=\"hpo-HP.580000325\"> </a></td><td>Triangular face</td></tr><tr><td style=\"white-space:nowrap\">HP:0000160<a name=\"hpo-HP.580000160\"> </a></td><td>Narrow mouth</td></tr><tr><td style=\"white-space:nowrap\">HP:0009487<a name=\"hpo-HP.580009487\"> </a></td><td>Ulnar deviation of the hand</td></tr><tr><td style=\"white-space:nowrap\">HP:0001249<a name=\"hpo-HP.580001249\"> </a></td><td>Intellectual disability</td></tr><tr><td style=\"white-space:nowrap\">HP:0008064<a name=\"hpo-HP.580008064\"> </a></td><td>Ichthyosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0000311<a name=\"hpo-HP.580000311\"> </a></td><td>Round face</td></tr><tr><td style=\"white-space:nowrap\">HP:0001653<a name=\"hpo-HP.580001653\"> </a></td><td>Mitral regurgitation</td></tr><tr><td style=\"white-space:nowrap\">HP:0001771<a name=\"hpo-HP.580001771\"> </a></td><td>Achilles tendon contracture</td></tr><tr><td style=\"white-space:nowrap\">HP:0012032<a name=\"hpo-HP.580012032\"> </a></td><td>Lipoma</td></tr><tr><td style=\"white-space:nowrap\">HP:0012368<a name=\"hpo-HP.580012368\"> </a></td><td>Flat face</td></tr><tr><td style=\"white-space:nowrap\">HP:0030053<a name=\"hpo-HP.580030053\"> </a></td><td>Stiff skin</td></tr><tr><td style=\"white-space:nowrap\">HP:0011124<a name=\"hpo-HP.580011124\"> </a></td><td>Abnormality of epidermal morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0011097<a name=\"hpo-HP.580011097\"> </a></td><td>Epileptic spasm</td></tr><tr><td style=\"white-space:nowrap\">HP:0000407<a name=\"hpo-HP.580000407\"> </a></td><td>Sensorineural hearing impairment</td></tr><tr><td style=\"white-space:nowrap\">HP:0000331<a name=\"hpo-HP.580000331\"> </a></td><td>Short chin</td></tr><tr><td style=\"white-space:nowrap\">HP:0000340<a name=\"hpo-HP.580000340\"> </a></td><td>Sloping forehead</td></tr><tr><td style=\"white-space:nowrap\">HP:0000486<a name=\"hpo-HP.580000486\"> </a></td><td>Strabismus</td></tr><tr><td style=\"white-space:nowrap\">HP:0000713<a name=\"hpo-HP.580000713\"> </a></td><td>Agitation</td></tr><tr><td style=\"white-space:nowrap\">HP:0000802<a name=\"hpo-HP.580000802\"> </a></td><td>Impotence</td></tr><tr><td style=\"white-space:nowrap\">HP:0001272<a name=\"hpo-HP.580001272\"> </a></td><td>Cerebellar atrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0001276<a name=\"hpo-HP.580001276\"> </a></td><td>Hypertonia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001321<a name=\"hpo-HP.580001321\"> </a></td><td>Cerebellar hypoplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001322<a name=\"hpo-HP.580001322\"> </a></td><td>obsolete Brain very small</td></tr><tr><td style=\"white-space:nowrap\">HP:0002061<a name=\"hpo-HP.580002061\"> </a></td><td>Lower limb spasticity</td></tr><tr><td style=\"white-space:nowrap\">HP:0002529<a name=\"hpo-HP.580002529\"> </a></td><td>Neuronal loss in central nervous system</td></tr><tr><td style=\"white-space:nowrap\">HP:0002540<a name=\"hpo-HP.580002540\"> </a></td><td>Inability to walk</td></tr><tr><td style=\"white-space:nowrap\">HP:0005484<a name=\"hpo-HP.580005484\"> </a></td><td>Postnatal microcephaly</td></tr><tr><td style=\"white-space:nowrap\">HP:0012850<a name=\"hpo-HP.580012850\"> </a></td><td>Small intestinal dysmotility</td></tr><tr><td style=\"white-space:nowrap\">HP:0000504<a name=\"hpo-HP.580000504\"> </a></td><td>Abnormality of vision</td></tr><tr><td style=\"white-space:nowrap\">HP:0002118<a name=\"hpo-HP.580002118\"> </a></td><td>Abnormality of the cerebral ventricles</td></tr><tr><td style=\"white-space:nowrap\">HP:0002363<a name=\"hpo-HP.580002363\"> </a></td><td>Abnormality of brainstem morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0010651<a name=\"hpo-HP.580010651\"> </a></td><td>Abnormal meningeal morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0100024<a name=\"hpo-HP.580100024\"> </a></td><td>Conspicuously happy disposition</td></tr><tr><td style=\"white-space:nowrap\">HP:0002538<a name=\"hpo-HP.580002538\"> </a></td><td>Abnormality of the cerebral cortex</td></tr><tr><td style=\"white-space:nowrap\">HP:0000054<a name=\"hpo-HP.580000054\"> </a></td><td>Micropenis</td></tr><tr><td style=\"white-space:nowrap\">HP:0000215<a name=\"hpo-HP.580000215\"> </a></td><td>Thick upper lip vermilion</td></tr><tr><td style=\"white-space:nowrap\">HP:0000293<a name=\"hpo-HP.580000293\"> </a></td><td>Full cheeks</td></tr><tr><td style=\"white-space:nowrap\">HP:0000349<a name=\"hpo-HP.580000349\"> </a></td><td>Widow's peak</td></tr><tr><td style=\"white-space:nowrap\">HP:0000444<a name=\"hpo-HP.580000444\"> </a></td><td>Convex nasal ridge</td></tr><tr><td style=\"white-space:nowrap\">HP:0000506<a name=\"hpo-HP.580000506\"> </a></td><td>Telecanthus</td></tr><tr><td style=\"white-space:nowrap\">HP:0000592<a name=\"hpo-HP.580000592\"> </a></td><td>Blue sclerae</td></tr><tr><td style=\"white-space:nowrap\">HP:0000691<a name=\"hpo-HP.580000691\"> </a></td><td>Microdontia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000698<a name=\"hpo-HP.580000698\"> </a></td><td>Conical tooth</td></tr><tr><td style=\"white-space:nowrap\">HP:0002000<a name=\"hpo-HP.580002000\"> </a></td><td>Short columella</td></tr><tr><td style=\"white-space:nowrap\">HP:0002097<a name=\"hpo-HP.580002097\"> </a></td><td>Emphysema</td></tr><tr><td style=\"white-space:nowrap\">HP:0002209<a name=\"hpo-HP.580002209\"> </a></td><td>Sparse scalp hair</td></tr><tr><td style=\"white-space:nowrap\">HP:0002816<a name=\"hpo-HP.580002816\"> </a></td><td>Genu recurvatum</td></tr><tr><td style=\"white-space:nowrap\">HP:0005116<a name=\"hpo-HP.580005116\"> </a></td><td>Arterial tortuosity</td></tr><tr><td style=\"white-space:nowrap\">HP:0007957<a name=\"hpo-HP.580007957\"> </a></td><td>Corneal opacity</td></tr><tr><td style=\"white-space:nowrap\">HP:0008070<a name=\"hpo-HP.580008070\"> </a></td><td>Sparse hair</td></tr><tr><td style=\"white-space:nowrap\">HP:0009623<a name=\"hpo-HP.580009623\"> </a></td><td>Proximal placement of thumb</td></tr><tr><td style=\"white-space:nowrap\">HP:0010055<a name=\"hpo-HP.580010055\"> </a></td><td>Broad hallux</td></tr><tr><td style=\"white-space:nowrap\">HP:0011318<a name=\"hpo-HP.580011318\"> </a></td><td>Bicoronal synostosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0011968<a name=\"hpo-HP.580011968\"> </a></td><td>Feeding difficulties</td></tr><tr><td style=\"white-space:nowrap\">HP:0200067<a name=\"hpo-HP.580200067\"> </a></td><td>Recurrent spontaneous abortion</td></tr><tr><td style=\"white-space:nowrap\">HP:0011819<a name=\"hpo-HP.580011819\"> </a></td><td>Submucous cleft soft palate</td></tr><tr><td style=\"white-space:nowrap\">HP:0000268<a name=\"hpo-HP.580000268\"> </a></td><td>Dolichocephaly</td></tr><tr><td style=\"white-space:nowrap\">HP:0003302<a name=\"hpo-HP.580003302\"> </a></td><td>Spondylolisthesis</td></tr><tr><td style=\"white-space:nowrap\">HP:0000582<a name=\"hpo-HP.580000582\"> </a></td><td>Upslanted palpebral fissure</td></tr><tr><td style=\"white-space:nowrap\">HP:0000952<a name=\"hpo-HP.580000952\"> </a></td><td>Jaundice</td></tr><tr><td style=\"white-space:nowrap\">HP:0001298<a name=\"hpo-HP.580001298\"> </a></td><td>Encephalopathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0001396<a name=\"hpo-HP.580001396\"> </a></td><td>Cholestasis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002059<a name=\"hpo-HP.580002059\"> </a></td><td>Cerebral atrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0002171<a name=\"hpo-HP.580002171\"> </a></td><td>Gliosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002240<a name=\"hpo-HP.580002240\"> </a></td><td>Hepatomegaly</td></tr><tr><td style=\"white-space:nowrap\">HP:0002353<a name=\"hpo-HP.580002353\"> </a></td><td>EEG abnormality</td></tr><tr><td style=\"white-space:nowrap\">HP:0002446<a name=\"hpo-HP.580002446\"> </a></td><td>Astrocytosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0003287<a name=\"hpo-HP.580003287\"> </a></td><td>Abnormality of mitochondrial metabolism</td></tr><tr><td style=\"white-space:nowrap\">HP:0011449<a name=\"hpo-HP.580011449\"> </a></td><td>Knee clonus</td></tr><tr><td style=\"white-space:nowrap\">HP:0012852<a name=\"hpo-HP.580012852\"> </a></td><td>Hepatic bridging fibrosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0100626<a name=\"hpo-HP.580100626\"> </a></td><td>Chronic hepatic failure</td></tr><tr><td style=\"white-space:nowrap\">HP:0000385<a name=\"hpo-HP.580000385\"> </a></td><td>Small earlobe</td></tr><tr><td style=\"white-space:nowrap\">HP:0009748<a name=\"hpo-HP.580009748\"> </a></td><td>Large earlobe</td></tr><tr><td style=\"white-space:nowrap\">HP:0000157<a name=\"hpo-HP.580000157\"> </a></td><td>Abnormality of the tongue</td></tr><tr><td style=\"white-space:nowrap\">HP:0000172<a name=\"hpo-HP.580000172\"> </a></td><td>Abnormality of the uvula</td></tr><tr><td style=\"white-space:nowrap\">HP:0000174<a name=\"hpo-HP.580000174\"> </a></td><td>Abnormal palate morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0000306<a name=\"hpo-HP.580000306\"> </a></td><td>Abnormality of the chin</td></tr><tr><td style=\"white-space:nowrap\">HP:0004408<a name=\"hpo-HP.580004408\"> </a></td><td>Abnormality of the sense of smell</td></tr><tr><td style=\"white-space:nowrap\">HP:0009912<a name=\"hpo-HP.580009912\"> </a></td><td>Abnormality of the tragus</td></tr><tr><td style=\"white-space:nowrap\">HP:0000537<a name=\"hpo-HP.580000537\"> </a></td><td>Epicanthus inversus</td></tr><tr><td style=\"white-space:nowrap\">HP:0000565<a name=\"hpo-HP.580000565\"> </a></td><td>Esotropia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000752<a name=\"hpo-HP.580000752\"> </a></td><td>Hyperactivity</td></tr><tr><td style=\"white-space:nowrap\">HP:0003186<a name=\"hpo-HP.580003186\"> </a></td><td>Inverted nipples</td></tr><tr><td style=\"white-space:nowrap\">HP:0012503<a name=\"hpo-HP.580012503\"> </a></td><td>Abnormality of the pituitary gland</td></tr><tr><td style=\"white-space:nowrap\">HP:0100710<a name=\"hpo-HP.580100710\"> </a></td><td>Impulsivity</td></tr><tr><td style=\"white-space:nowrap\">HP:0000357<a name=\"hpo-HP.580000357\"> </a></td><td>Abnormal location of ears</td></tr><tr><td style=\"white-space:nowrap\">HP:0000820<a name=\"hpo-HP.580000820\"> </a></td><td>Abnormality of the thyroid gland</td></tr><tr><td style=\"white-space:nowrap\">HP:0000828<a name=\"hpo-HP.580000828\"> </a></td><td>Abnormality of the parathyroid gland</td></tr><tr><td style=\"white-space:nowrap\">HP:0000834<a name=\"hpo-HP.580000834\"> </a></td><td>Abnormality of the adrenal glands</td></tr><tr><td style=\"white-space:nowrap\">HP:0012093<a name=\"hpo-HP.580012093\"> </a></td><td>Abnormality of endocrine pancreas physiology</td></tr><tr><td style=\"white-space:nowrap\">HP:0000269<a name=\"hpo-HP.580000269\"> </a></td><td>Prominent occiput</td></tr><tr><td style=\"white-space:nowrap\">HP:0000535<a name=\"hpo-HP.580000535\"> </a></td><td>Sparse and thin eyebrow</td></tr><tr><td style=\"white-space:nowrap\">HP:0000639<a name=\"hpo-HP.580000639\"> </a></td><td>Nystagmus</td></tr><tr><td style=\"white-space:nowrap\">HP:0000718<a name=\"hpo-HP.580000718\"> </a></td><td>Aggressive behavior</td></tr><tr><td style=\"white-space:nowrap\">HP:0000957<a name=\"hpo-HP.580000957\"> </a></td><td>Cafe-au-lait spot</td></tr><tr><td style=\"white-space:nowrap\">HP:0000256<a name=\"hpo-HP.580000256\"> </a></td><td>Macrocephaly</td></tr><tr><td style=\"white-space:nowrap\">HP:0000750<a name=\"hpo-HP.580000750\"> </a></td><td>Delayed speech and language development</td></tr><tr><td style=\"white-space:nowrap\">HP:0000963<a name=\"hpo-HP.580000963\"> </a></td><td>Thin skin</td></tr><tr><td style=\"white-space:nowrap\">HP:0001260<a name=\"hpo-HP.580001260\"> </a></td><td>Dysarthria</td></tr><tr><td style=\"white-space:nowrap\">HP:0002194<a name=\"hpo-HP.580002194\"> </a></td><td>Delayed gross motor development</td></tr><tr><td style=\"white-space:nowrap\">HP:0003196<a name=\"hpo-HP.580003196\"> </a></td><td>Short nose</td></tr><tr><td style=\"white-space:nowrap\">HP:0001155<a name=\"hpo-HP.580001155\"> </a></td><td>Abnormality of the hand</td></tr><tr><td style=\"white-space:nowrap\">HP:0100022<a name=\"hpo-HP.580100022\"> </a></td><td>Abnormality of movement</td></tr><tr><td style=\"white-space:nowrap\">HP:0010862<a name=\"hpo-HP.580010862\"> </a></td><td>Delayed fine motor development</td></tr><tr><td style=\"white-space:nowrap\">HP:0000343<a name=\"hpo-HP.580000343\"> </a></td><td>Long philtrum</td></tr><tr><td style=\"white-space:nowrap\">HP:0000717<a name=\"hpo-HP.580000717\"> </a></td><td>Autism</td></tr><tr><td style=\"white-space:nowrap\">HP:0001883<a name=\"hpo-HP.580001883\"> </a></td><td>Talipes</td></tr><tr><td style=\"white-space:nowrap\">HP:0002553<a name=\"hpo-HP.580002553\"> </a></td><td>Highly arched eyebrow</td></tr><tr><td style=\"white-space:nowrap\">HP:0007488<a name=\"hpo-HP.580007488\"> </a></td><td>Diffuse skin atrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0000822<a name=\"hpo-HP.580000822\"> </a></td><td>Hypertension</td></tr><tr><td style=\"white-space:nowrap\">HP:0001278<a name=\"hpo-HP.580001278\"> </a></td><td>Orthostatic hypotension</td></tr><tr><td style=\"white-space:nowrap\">HP:0001944<a name=\"hpo-HP.580001944\"> </a></td><td>Dehydration</td></tr><tr><td style=\"white-space:nowrap\">HP:0001945<a name=\"hpo-HP.580001945\"> </a></td><td>Fever</td></tr><tr><td style=\"white-space:nowrap\">HP:0002019<a name=\"hpo-HP.580002019\"> </a></td><td>Constipation</td></tr><tr><td style=\"white-space:nowrap\">HP:0002020<a name=\"hpo-HP.580002020\"> </a></td><td>Gastroesophageal reflux</td></tr><tr><td style=\"white-space:nowrap\">HP:0002027<a name=\"hpo-HP.580002027\"> </a></td><td>Abdominal pain</td></tr><tr><td style=\"white-space:nowrap\">HP:0002718<a name=\"hpo-HP.580002718\"> </a></td><td>Recurrent bacterial infections</td></tr><tr><td style=\"white-space:nowrap\">HP:0002841<a name=\"hpo-HP.580002841\"> </a></td><td>Recurrent fungal infections</td></tr><tr><td style=\"white-space:nowrap\">HP:0004395<a name=\"hpo-HP.580004395\"> </a></td><td>Malnutrition</td></tr><tr><td style=\"white-space:nowrap\">HP:0009830<a name=\"hpo-HP.580009830\"> </a></td><td>Peripheral neuropathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0000126<a name=\"hpo-HP.580000126\"> </a></td><td>Hydronephrosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0000519<a name=\"hpo-HP.580000519\"> </a></td><td>Developmental cataract</td></tr><tr><td style=\"white-space:nowrap\">HP:0000648<a name=\"hpo-HP.580000648\"> </a></td><td>Optic atrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0001053<a name=\"hpo-HP.580001053\"> </a></td><td>Hypopigmented skin patches</td></tr><tr><td style=\"white-space:nowrap\">HP:0001087<a name=\"hpo-HP.580001087\"> </a></td><td>Developmental glaucoma</td></tr><tr><td style=\"white-space:nowrap\">HP:0002119<a name=\"hpo-HP.580002119\"> </a></td><td>Ventriculomegaly</td></tr><tr><td style=\"white-space:nowrap\">HP:0002280<a name=\"hpo-HP.580002280\"> </a></td><td>Enlarged cisterna magna</td></tr><tr><td style=\"white-space:nowrap\">HP:0003298<a name=\"hpo-HP.580003298\"> </a></td><td>Spina bifida occulta</td></tr><tr><td style=\"white-space:nowrap\">HP:0004467<a name=\"hpo-HP.580004467\"> </a></td><td>Preauricular pit</td></tr><tr><td style=\"white-space:nowrap\">HP:0008511<a name=\"hpo-HP.580008511\"> </a></td><td>Central posterior corneal opacity</td></tr><tr><td style=\"white-space:nowrap\">HP:0010780<a name=\"hpo-HP.580010780\"> </a></td><td>Hyperacusis</td></tr><tr><td style=\"white-space:nowrap\">HP:0030048<a name=\"hpo-HP.580030048\"> </a></td><td>Colpocephaly</td></tr><tr><td style=\"white-space:nowrap\">HP:0100335<a name=\"hpo-HP.580100335\"> </a></td><td>Non-midline cleft lip</td></tr><tr><td style=\"white-space:nowrap\">HP:0000525<a name=\"hpo-HP.580000525\"> </a></td><td>Abnormality iris morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0002719<a name=\"hpo-HP.580002719\"> </a></td><td>Recurrent infections</td></tr><tr><td style=\"white-space:nowrap\">HP:0000153<a name=\"hpo-HP.580000153\"> </a></td><td>Abnormality of the mouth</td></tr><tr><td style=\"white-space:nowrap\">HP:0001903<a name=\"hpo-HP.580001903\"> </a></td><td>Anemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002094<a name=\"hpo-HP.580002094\"> </a></td><td>Dyspnea</td></tr><tr><td style=\"white-space:nowrap\">HP:0002206<a name=\"hpo-HP.580002206\"> </a></td><td>Pulmonary fibrosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002789<a name=\"hpo-HP.580002789\"> </a></td><td>Tachypnea</td></tr><tr><td style=\"white-space:nowrap\">HP:0002793<a name=\"hpo-HP.580002793\"> </a></td><td>Abnormal pattern of respiration</td></tr><tr><td style=\"white-space:nowrap\">HP:0003565<a name=\"hpo-HP.580003565\"> </a></td><td>Elevated erythrocyte sedimentation rate</td></tr><tr><td style=\"white-space:nowrap\">HP:0006517<a name=\"hpo-HP.580006517\"> </a></td><td>Intraalveolar phospholipid accumulation</td></tr><tr><td style=\"white-space:nowrap\">HP:0006530<a name=\"hpo-HP.580006530\"> </a></td><td>Interstitial pulmonary abnormality</td></tr><tr><td style=\"white-space:nowrap\">HP:0100759<a name=\"hpo-HP.580100759\"> </a></td><td>Clubbing of fingers</td></tr><tr><td style=\"white-space:nowrap\">HP:0002103<a name=\"hpo-HP.580002103\"> </a></td><td>Abnormal pleura morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0001596<a name=\"hpo-HP.580001596\"> </a></td><td>Alopecia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001882<a name=\"hpo-HP.580001882\"> </a></td><td>Leukopenia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002013<a name=\"hpo-HP.580002013\"> </a></td><td>Vomiting</td></tr><tr><td style=\"white-space:nowrap\">HP:0002028<a name=\"hpo-HP.580002028\"> </a></td><td>Chronic diarrhea</td></tr><tr><td style=\"white-space:nowrap\">HP:0002573<a name=\"hpo-HP.580002573\"> </a></td><td>Hematochezia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002960<a name=\"hpo-HP.580002960\"> </a></td><td>Autoimmunity</td></tr><tr><td style=\"white-space:nowrap\">HP:0005387<a name=\"hpo-HP.580005387\"> </a></td><td>Combined immunodeficiency</td></tr><tr><td style=\"white-space:nowrap\">HP:0011109<a name=\"hpo-HP.580011109\"> </a></td><td>Chronic sinusitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0004429<a name=\"hpo-HP.580004429\"> </a></td><td>Recurrent viral infections</td></tr><tr><td style=\"white-space:nowrap\">HP:0000280<a name=\"hpo-HP.580000280\"> </a></td><td>Coarse facial features</td></tr><tr><td style=\"white-space:nowrap\">HP:0000294<a name=\"hpo-HP.580000294\"> </a></td><td>Low anterior hairline</td></tr><tr><td style=\"white-space:nowrap\">HP:0000577<a name=\"hpo-HP.580000577\"> </a></td><td>Exotropia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001873<a name=\"hpo-HP.580001873\"> </a></td><td>Thrombocytopenia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002011<a name=\"hpo-HP.580002011\"> </a></td><td>Morphological central nervous system abnormality</td></tr><tr><td style=\"white-space:nowrap\">HP:0006610<a name=\"hpo-HP.580006610\"> </a></td><td>Wide intermamillary distance</td></tr><tr><td style=\"white-space:nowrap\">HP:0011231<a name=\"hpo-HP.580011231\"> </a></td><td>Prominent eyelashes</td></tr><tr><td style=\"white-space:nowrap\">HP:0012718<a name=\"hpo-HP.580012718\"> </a></td><td>Morphological abnormality of the gastrointestinal tract</td></tr><tr><td style=\"white-space:nowrap\">HP:0002024<a name=\"hpo-HP.580002024\"> </a></td><td>Malabsorption</td></tr><tr><td style=\"white-space:nowrap\">HP:0001394<a name=\"hpo-HP.580001394\"> </a></td><td>Cirrhosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001414<a name=\"hpo-HP.580001414\"> </a></td><td>Microvesicular hepatic steatosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001403<a name=\"hpo-HP.580001403\"> </a></td><td>Macrovesicular hepatic steatosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001410<a name=\"hpo-HP.580001410\"> </a></td><td>Decreased liver function</td></tr><tr><td style=\"white-space:nowrap\">HP:0001409<a name=\"hpo-HP.580001409\"> </a></td><td>Portal hypertension</td></tr><tr><td style=\"white-space:nowrap\">HP:0001744<a name=\"hpo-HP.580001744\"> </a></td><td>Splenomegaly</td></tr><tr><td style=\"white-space:nowrap\">HP:0003394<a name=\"hpo-HP.580003394\"> </a></td><td>Muscle spasm</td></tr><tr><td style=\"white-space:nowrap\">HP:0003750<a name=\"hpo-HP.580003750\"> </a></td><td>Increased muscle fatiguability</td></tr><tr><td style=\"white-space:nowrap\">HP:0002123<a name=\"hpo-HP.580002123\"> </a></td><td>Generalized myoclonic seizure</td></tr><tr><td style=\"white-space:nowrap\">HP:0002219<a name=\"hpo-HP.580002219\"> </a></td><td>Facial hypertrichosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0000831<a name=\"hpo-HP.580000831\"> </a></td><td>Insulin-resistant diabetes mellitus</td></tr><tr><td style=\"white-space:nowrap\">HP:0001891<a name=\"hpo-HP.580001891\"> </a></td><td>Iron deficiency anemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001264<a name=\"hpo-HP.580001264\"> </a></td><td>Spastic diplegia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002313<a name=\"hpo-HP.580002313\"> </a></td><td>Spastic paraparesis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001347<a name=\"hpo-HP.580001347\"> </a></td><td>Hyperreflexia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002460<a name=\"hpo-HP.580002460\"> </a></td><td>Distal muscle weakness</td></tr><tr><td style=\"white-space:nowrap\">HP:0000763<a name=\"hpo-HP.580000763\"> </a></td><td>Sensory neuropathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0001268<a name=\"hpo-HP.580001268\"> </a></td><td>Mental deterioration</td></tr><tr><td style=\"white-space:nowrap\">HP:0002169<a name=\"hpo-HP.580002169\"> </a></td><td>Clonus</td></tr><tr><td style=\"white-space:nowrap\">HP:0001332<a name=\"hpo-HP.580001332\"> </a></td><td>Dystonia</td></tr><tr><td style=\"white-space:nowrap\">HP:0100716<a name=\"hpo-HP.580100716\"> </a></td><td>Self-injurious behavior</td></tr><tr><td style=\"white-space:nowrap\">HP:0000602<a name=\"hpo-HP.580000602\"> </a></td><td>Ophthalmoplegia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001251<a name=\"hpo-HP.580001251\"> </a></td><td>Ataxia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000776<a name=\"hpo-HP.580000776\"> </a></td><td>Congenital diaphragmatic hernia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000410<a name=\"hpo-HP.580000410\"> </a></td><td>Mixed hearing impairment</td></tr><tr><td style=\"white-space:nowrap\">HP:0000510<a name=\"hpo-HP.580000510\"> </a></td><td>Rod-cone dystrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0004437<a name=\"hpo-HP.580004437\"> </a></td><td>Cranial hyperostosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0011001<a name=\"hpo-HP.580011001\"> </a></td><td>Increased bone mineral density</td></tr><tr><td style=\"white-space:nowrap\">HP:0000956<a name=\"hpo-HP.580000956\"> </a></td><td>Acanthosis nigricans</td></tr><tr><td style=\"white-space:nowrap\">HP:0000958<a name=\"hpo-HP.580000958\"> </a></td><td>Dry skin</td></tr><tr><td style=\"white-space:nowrap\">HP:0000580<a name=\"hpo-HP.580000580\"> </a></td><td>Pigmentary retinopathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0000649<a name=\"hpo-HP.580000649\"> </a></td><td>Abnormality of visual evoked potentials</td></tr><tr><td style=\"white-space:nowrap\">HP:0000657<a name=\"hpo-HP.580000657\"> </a></td><td>Oculomotor apraxia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000479<a name=\"hpo-HP.580000479\"> </a></td><td>Abnormal retinal morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0001317<a name=\"hpo-HP.580001317\"> </a></td><td>Abnormal cerebellum morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0001533<a name=\"hpo-HP.580001533\"> </a></td><td>Slender build</td></tr><tr><td style=\"white-space:nowrap\">HP:0001629<a name=\"hpo-HP.580001629\"> </a></td><td>Ventricular septal defect</td></tr><tr><td style=\"white-space:nowrap\">HP:0000703<a name=\"hpo-HP.580000703\"> </a></td><td>Dentinogenesis imperfecta</td></tr><tr><td style=\"white-space:nowrap\">HP:0000914<a name=\"hpo-HP.580000914\"> </a></td><td>Shield chest</td></tr><tr><td style=\"white-space:nowrap\">HP:0001500<a name=\"hpo-HP.580001500\"> </a></td><td>Broad finger</td></tr><tr><td style=\"white-space:nowrap\">HP:0003086<a name=\"hpo-HP.580003086\"> </a></td><td>Acromesomelia</td></tr><tr><td style=\"white-space:nowrap\">HP:0003416<a name=\"hpo-HP.580003416\"> </a></td><td>Spinal canal stenosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002815<a name=\"hpo-HP.580002815\"> </a></td><td>Abnormality of the knee</td></tr><tr><td style=\"white-space:nowrap\">HP:0002992<a name=\"hpo-HP.580002992\"> </a></td><td>Abnormality of tibia morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0001639<a name=\"hpo-HP.580001639\"> </a></td><td>Hypertrophic cardiomyopathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0003236<a name=\"hpo-HP.580003236\"> </a></td><td>Elevated serum creatine kinase</td></tr><tr><td style=\"white-space:nowrap\">HP:0001369<a name=\"hpo-HP.580001369\"> </a></td><td>Arthritis</td></tr><tr><td style=\"white-space:nowrap\">HP:0003560<a name=\"hpo-HP.580003560\"> </a></td><td>Muscular dystrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0003974<a name=\"hpo-HP.580003974\"> </a></td><td>Absent radius</td></tr><tr><td style=\"white-space:nowrap\">HP:0002818<a name=\"hpo-HP.580002818\"> </a></td><td>Abnormality of the radius</td></tr><tr><td style=\"white-space:nowrap\">HP:0001561<a name=\"hpo-HP.580001561\"> </a></td><td>Polyhydramnios</td></tr><tr><td style=\"white-space:nowrap\">HP:0002299<a name=\"hpo-HP.580002299\"> </a></td><td>Brittle hair</td></tr><tr><td style=\"white-space:nowrap\">HP:0002208<a name=\"hpo-HP.580002208\"> </a></td><td>Coarse hair</td></tr><tr><td style=\"white-space:nowrap\">HP:0002213<a name=\"hpo-HP.580002213\"> </a></td><td>Fine hair</td></tr><tr><td style=\"white-space:nowrap\">HP:0000522<a name=\"hpo-HP.580000522\"> </a></td><td>Alacrima</td></tr><tr><td style=\"white-space:nowrap\">HP:0100704<a name=\"hpo-HP.580100704\"> </a></td><td>Cerebral visual impairment</td></tr><tr><td style=\"white-space:nowrap\">HP:0012713<a name=\"hpo-HP.580012713\"> </a></td><td>Moderate hearing impairment</td></tr><tr><td style=\"white-space:nowrap\">HP:0002307<a name=\"hpo-HP.580002307\"> </a></td><td>Drooling</td></tr><tr><td style=\"white-space:nowrap\">HP:0002714<a name=\"hpo-HP.580002714\"> </a></td><td>Downturned corners of mouth</td></tr><tr><td style=\"white-space:nowrap\">HP:0000191<a name=\"hpo-HP.580000191\"> </a></td><td>Accessory oral frenulum</td></tr><tr><td style=\"white-space:nowrap\">HP:0000158<a name=\"hpo-HP.580000158\"> </a></td><td>Macroglossia</td></tr><tr><td style=\"white-space:nowrap\">HP:0012020<a name=\"hpo-HP.580012020\"> </a></td><td>Right aortic arch</td></tr><tr><td style=\"white-space:nowrap\">HP:0002104<a name=\"hpo-HP.580002104\"> </a></td><td>Apnea</td></tr><tr><td style=\"white-space:nowrap\">HP:0000598<a name=\"hpo-HP.580000598\"> </a></td><td>Abnormality of the ear</td></tr><tr><td style=\"white-space:nowrap\">HP:0007874<a name=\"hpo-HP.580007874\"> </a></td><td>Almond-shaped palpebral fissure</td></tr><tr><td style=\"white-space:nowrap\">HP:0010804<a name=\"hpo-HP.580010804\"> </a></td><td>Tented upper lip vermilion</td></tr><tr><td style=\"white-space:nowrap\">HP:0000885<a name=\"hpo-HP.580000885\"> </a></td><td>Broad ribs</td></tr><tr><td style=\"white-space:nowrap\">HP:0000768<a name=\"hpo-HP.580000768\"> </a></td><td>Pectus carinatum</td></tr><tr><td style=\"white-space:nowrap\">HP:0001680<a name=\"hpo-HP.580001680\"> </a></td><td>Coarctation of aorta</td></tr><tr><td style=\"white-space:nowrap\">HP:0000687<a name=\"hpo-HP.580000687\"> </a></td><td>Widely spaced teeth</td></tr><tr><td style=\"white-space:nowrap\">HP:0000047<a name=\"hpo-HP.580000047\"> </a></td><td>Hypospadias</td></tr><tr><td style=\"white-space:nowrap\">HP:0001943<a name=\"hpo-HP.580001943\"> </a></td><td>Hypoglycemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0012369<a name=\"hpo-HP.580012369\"> </a></td><td>Abnormality of malar bones</td></tr><tr><td style=\"white-space:nowrap\">HP:0009900<a name=\"hpo-HP.580009900\"> </a></td><td>Unilateral deafness</td></tr><tr><td style=\"white-space:nowrap\">HP:0000023<a name=\"hpo-HP.580000023\"> </a></td><td>Inguinal hernia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000074<a name=\"hpo-HP.580000074\"> </a></td><td>Ureteropelvic junction obstruction</td></tr><tr><td style=\"white-space:nowrap\">HP:0001800<a name=\"hpo-HP.580001800\"> </a></td><td>Hypoplastic toenails</td></tr><tr><td style=\"white-space:nowrap\">HP:0001804<a name=\"hpo-HP.580001804\"> </a></td><td>Hypoplastic fingernail</td></tr><tr><td style=\"white-space:nowrap\">HP:0002949<a name=\"hpo-HP.580002949\"> </a></td><td>Fused cervical vertebrae</td></tr><tr><td style=\"white-space:nowrap\">HP:0008050<a name=\"hpo-HP.580008050\"> </a></td><td>Abnormality of the palpebral fissures</td></tr><tr><td style=\"white-space:nowrap\">HP:0008577<a name=\"hpo-HP.580008577\"> </a></td><td>Underfolded helix</td></tr><tr><td style=\"white-space:nowrap\">HP:0008589<a name=\"hpo-HP.580008589\"> </a></td><td>Hypoplastic helices</td></tr><tr><td style=\"white-space:nowrap\">HP:0010863<a name=\"hpo-HP.580010863\"> </a></td><td>Receptive language delay</td></tr><tr><td style=\"white-space:nowrap\">HP:0002282<a name=\"hpo-HP.580002282\"> </a></td><td>Gray matter heterotopia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002085<a name=\"hpo-HP.580002085\"> </a></td><td>Occipital encephalocele</td></tr><tr><td style=\"white-space:nowrap\">HP:0001057<a name=\"hpo-HP.580001057\"> </a></td><td>Aplasia cutis congenita</td></tr><tr><td style=\"white-space:nowrap\">HP:0000211<a name=\"hpo-HP.580000211\"> </a></td><td>Trismus</td></tr><tr><td style=\"white-space:nowrap\">HP:0008422<a name=\"hpo-HP.580008422\"> </a></td><td>Vertebral wedging</td></tr><tr><td style=\"white-space:nowrap\">HP:0003170<a name=\"hpo-HP.580003170\"> </a></td><td>Abnormality of the acetabulum</td></tr><tr><td style=\"white-space:nowrap\">HP:0003272<a name=\"hpo-HP.580003272\"> </a></td><td>Abnormality of the hip bone</td></tr><tr><td style=\"white-space:nowrap\">HP:0003028<a name=\"hpo-HP.580003028\"> </a></td><td>Abnormality of the ankles</td></tr><tr><td style=\"white-space:nowrap\">HP:0003301<a name=\"hpo-HP.580003301\"> </a></td><td>Irregular vertebral endplates</td></tr><tr><td style=\"white-space:nowrap\">HP:0010508<a name=\"hpo-HP.580010508\"> </a></td><td>Metatarsus valgus</td></tr><tr><td style=\"white-space:nowrap\">HP:0009811<a name=\"hpo-HP.580009811\"> </a></td><td>Abnormality of the elbow</td></tr><tr><td style=\"white-space:nowrap\">HP:0000736<a name=\"hpo-HP.580000736\"> </a></td><td>Short attention span</td></tr><tr><td style=\"white-space:nowrap\">HP:0002912<a name=\"hpo-HP.580002912\"> </a></td><td>Methylmalonic acidemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001941<a name=\"hpo-HP.580001941\"> </a></td><td>Acidosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001992<a name=\"hpo-HP.580001992\"> </a></td><td>Organic aciduria</td></tr><tr><td style=\"white-space:nowrap\">HP:0009027<a name=\"hpo-HP.580009027\"> </a></td><td>Foot dorsiflexor weakness</td></tr><tr><td style=\"white-space:nowrap\">HP:0002063<a name=\"hpo-HP.580002063\"> </a></td><td>Rigidity</td></tr><tr><td style=\"white-space:nowrap\">HP:0000384<a name=\"hpo-HP.580000384\"> </a></td><td>Preauricular skin tag</td></tr><tr><td style=\"white-space:nowrap\">HP:0200046<a name=\"hpo-HP.580200046\"> </a></td><td>Cat cry</td></tr><tr><td style=\"white-space:nowrap\">HP:0001357<a name=\"hpo-HP.580001357\"> </a></td><td>Plagiocephaly</td></tr><tr><td style=\"white-space:nowrap\">HP:0000670<a name=\"hpo-HP.580000670\"> </a></td><td>Carious teeth</td></tr><tr><td style=\"white-space:nowrap\">HP:0011090<a name=\"hpo-HP.580011090\"> </a></td><td>Fused teeth</td></tr><tr><td style=\"white-space:nowrap\">HP:0012810<a name=\"hpo-HP.580012810\"> </a></td><td>Wide nasal base</td></tr><tr><td style=\"white-space:nowrap\">HP:0010296<a name=\"hpo-HP.580010296\"> </a></td><td>Ankyloglossia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001636<a name=\"hpo-HP.580001636\"> </a></td><td>Tetralogy of Fallot</td></tr><tr><td style=\"white-space:nowrap\">HP:0001305<a name=\"hpo-HP.580001305\"> </a></td><td>Dandy-Walker malformation</td></tr><tr><td style=\"white-space:nowrap\">HP:0000238<a name=\"hpo-HP.580000238\"> </a></td><td>Hydrocephalus</td></tr><tr><td style=\"white-space:nowrap\">HP:0005469<a name=\"hpo-HP.580005469\"> </a></td><td>Flat occiput</td></tr><tr><td style=\"white-space:nowrap\">HP:0000270<a name=\"hpo-HP.580000270\"> </a></td><td>Delayed cranial suture closure</td></tr><tr><td style=\"white-space:nowrap\">HP:0000239<a name=\"hpo-HP.580000239\"> </a></td><td>Large fontanelles</td></tr><tr><td style=\"white-space:nowrap\">HP:0010537<a name=\"hpo-HP.580010537\"> </a></td><td>Wide cranial sutures</td></tr><tr><td style=\"white-space:nowrap\">HP:0002217<a name=\"hpo-HP.580002217\"> </a></td><td>Slow-growing hair</td></tr><tr><td style=\"white-space:nowrap\">HP:0000587<a name=\"hpo-HP.580000587\"> </a></td><td>Abnormality of the optic nerve</td></tr><tr><td style=\"white-space:nowrap\">HP:0005989<a name=\"hpo-HP.580005989\"> </a></td><td>Redundant neck skin</td></tr><tr><td style=\"white-space:nowrap\">HP:0010775<a name=\"hpo-HP.580010775\"> </a></td><td>Vascular ring</td></tr><tr><td style=\"white-space:nowrap\">HP:0002779<a name=\"hpo-HP.580002779\"> </a></td><td>Tracheomalacia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002827<a name=\"hpo-HP.580002827\"> </a></td><td>Hip dislocation</td></tr><tr><td style=\"white-space:nowrap\">HP:0001302<a name=\"hpo-HP.580001302\"> </a></td><td>Pachygyria</td></tr><tr><td style=\"white-space:nowrap\">HP:0007362<a name=\"hpo-HP.580007362\"> </a></td><td>Aplasia/Hypoplasia of the brainstem</td></tr><tr><td style=\"white-space:nowrap\">HP:0001558<a name=\"hpo-HP.580001558\"> </a></td><td>Decreased fetal movement</td></tr><tr><td style=\"white-space:nowrap\">HP:0010878<a name=\"hpo-HP.580010878\"> </a></td><td>Fetal cystic hygroma</td></tr><tr><td style=\"white-space:nowrap\">HP:0011398<a name=\"hpo-HP.580011398\"> </a></td><td>Central hypotonia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002071<a name=\"hpo-HP.580002071\"> </a></td><td>Abnormality of extrapyramidal motor function</td></tr><tr><td style=\"white-space:nowrap\">HP:0000826<a name=\"hpo-HP.580000826\"> </a></td><td>Precocious puberty</td></tr><tr><td style=\"white-space:nowrap\">HP:0000014<a name=\"hpo-HP.580000014\"> </a></td><td>Abnormality of the bladder</td></tr><tr><td style=\"white-space:nowrap\">HP:0005037<a name=\"hpo-HP.580005037\"> </a></td><td>Proximal radio-ulnar synostosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0100543<a name=\"hpo-HP.580100543\"> </a></td><td>Cognitive impairment</td></tr><tr><td style=\"white-space:nowrap\">HP:0000481<a name=\"hpo-HP.580000481\"> </a></td><td>Abnormal cornea morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0000076<a name=\"hpo-HP.580000076\"> </a></td><td>Vesicoureteral reflux</td></tr><tr><td style=\"white-space:nowrap\">HP:0000297<a name=\"hpo-HP.580000297\"> </a></td><td>Facial hypotonia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000391<a name=\"hpo-HP.580000391\"> </a></td><td>Thickened helices</td></tr><tr><td style=\"white-space:nowrap\">HP:0001162<a name=\"hpo-HP.580001162\"> </a></td><td>Postaxial hand polydactyly</td></tr><tr><td style=\"white-space:nowrap\">HP:0001385<a name=\"hpo-HP.580001385\"> </a></td><td>Hip dysplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002342<a name=\"hpo-HP.580002342\"> </a></td><td>Intellectual disability, moderate</td></tr><tr><td style=\"white-space:nowrap\">HP:0003191<a name=\"hpo-HP.580003191\"> </a></td><td>Cleft ala nasi</td></tr><tr><td style=\"white-space:nowrap\">HP:0009765<a name=\"hpo-HP.580009765\"> </a></td><td>Low hanging columella</td></tr><tr><td style=\"white-space:nowrap\">HP:0010297<a name=\"hpo-HP.580010297\"> </a></td><td>Bifid tongue</td></tr><tr><td style=\"white-space:nowrap\">HP:0011330<a name=\"hpo-HP.580011330\"> </a></td><td>Metopic synostosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0012804<a name=\"hpo-HP.580012804\"> </a></td><td>Corneal ulceration</td></tr><tr><td style=\"white-space:nowrap\">HP:0010485<a name=\"hpo-HP.580010485\"> </a></td><td>Hyperextensibility at elbow</td></tr><tr><td style=\"white-space:nowrap\">HP:0000609<a name=\"hpo-HP.580000609\"> </a></td><td>Optic nerve hypoplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001176<a name=\"hpo-HP.580001176\"> </a></td><td>Large hands</td></tr><tr><td style=\"white-space:nowrap\">HP:0004233<a name=\"hpo-HP.580004233\"> </a></td><td>Advanced ossification of carpal bones</td></tr><tr><td style=\"white-space:nowrap\">HP:0100842<a name=\"hpo-HP.580100842\"> </a></td><td>Septo-optic dysplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002034<a name=\"hpo-HP.580002034\"> </a></td><td>Abnormality of the rectum</td></tr><tr><td style=\"white-space:nowrap\">HP:0002283<a name=\"hpo-HP.580002283\"> </a></td><td>Global brain atrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0003115<a name=\"hpo-HP.580003115\"> </a></td><td>Abnormal EKG</td></tr><tr><td style=\"white-space:nowrap\">HP:0002577<a name=\"hpo-HP.580002577\"> </a></td><td>Abnormal stomach morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0002539<a name=\"hpo-HP.580002539\"> </a></td><td>Cortical dysplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0006818<a name=\"hpo-HP.580006818\"> </a></td><td>4-layered lissencephaly</td></tr><tr><td style=\"white-space:nowrap\">HP:0000593<a name=\"hpo-HP.580000593\"> </a></td><td>Abnormal anterior chamber morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0000179<a name=\"hpo-HP.580000179\"> </a></td><td>Thick lower lip vermilion</td></tr><tr><td style=\"white-space:nowrap\">HP:0002002<a name=\"hpo-HP.580002002\"> </a></td><td>Deep philtrum</td></tr><tr><td style=\"white-space:nowrap\">HP:0009931<a name=\"hpo-HP.580009931\"> </a></td><td>Enlarged naris</td></tr><tr><td style=\"white-space:nowrap\">HP:0002948<a name=\"hpo-HP.580002948\"> </a></td><td>Vertebral fusion</td></tr><tr><td style=\"white-space:nowrap\">HP:0002937<a name=\"hpo-HP.580002937\"> </a></td><td>Hemivertebrae</td></tr><tr><td style=\"white-space:nowrap\">HP:0002308<a name=\"hpo-HP.580002308\"> </a></td><td>Arnold-Chiari malformation</td></tr><tr><td style=\"white-space:nowrap\">HP:0011320<a name=\"hpo-HP.580011320\"> </a></td><td>Unilambdoid synostosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002781<a name=\"hpo-HP.580002781\"> </a></td><td>Upper airway obstruction</td></tr><tr><td style=\"white-space:nowrap\">HP:0001363<a name=\"hpo-HP.580001363\"> </a></td><td>Craniosynostosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0000204<a name=\"hpo-HP.580000204\"> </a></td><td>Cleft upper lip</td></tr><tr><td style=\"white-space:nowrap\">HP:0001738<a name=\"hpo-HP.580001738\"> </a></td><td>Exocrine pancreatic insufficiency</td></tr><tr><td style=\"white-space:nowrap\">HP:0002823<a name=\"hpo-HP.580002823\"> </a></td><td>Abnormality of femur morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0000823<a name=\"hpo-HP.580000823\"> </a></td><td>Delayed puberty</td></tr><tr><td style=\"white-space:nowrap\">HP:0100279<a name=\"hpo-HP.580100279\"> </a></td><td>Ulcerative colitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0003834<a name=\"hpo-HP.580003834\"> </a></td><td>Shoulder dislocation</td></tr><tr><td style=\"white-space:nowrap\">HP:0001065<a name=\"hpo-HP.580001065\"> </a></td><td>Striae distensae</td></tr><tr><td style=\"white-space:nowrap\">HP:0000448<a name=\"hpo-HP.580000448\"> </a></td><td>Prominent nose</td></tr><tr><td style=\"white-space:nowrap\">HP:0000554<a name=\"hpo-HP.580000554\"> </a></td><td>Uveitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001006<a name=\"hpo-HP.580001006\"> </a></td><td>obsolete Hypotrichosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0000501<a name=\"hpo-HP.580000501\"> </a></td><td>Glaucoma</td></tr><tr><td style=\"white-space:nowrap\">HP:0000262<a name=\"hpo-HP.580000262\"> </a></td><td>Turricephaly</td></tr><tr><td style=\"white-space:nowrap\">HP:0000729<a name=\"hpo-HP.580000729\"> </a></td><td>Autistic behavior</td></tr><tr><td style=\"white-space:nowrap\">HP:0010800<a name=\"hpo-HP.580010800\"> </a></td><td>Absent cupid's bow</td></tr><tr><td style=\"white-space:nowrap\">HP:0010808<a name=\"hpo-HP.580010808\"> </a></td><td>Protruding tongue</td></tr><tr><td style=\"white-space:nowrap\">HP:0009927<a name=\"hpo-HP.580009927\"> </a></td><td>Aplasia of the nose</td></tr><tr><td style=\"white-space:nowrap\">HP:0100539<a name=\"hpo-HP.580100539\"> </a></td><td>Periorbital edema</td></tr><tr><td style=\"white-space:nowrap\">HP:0000629<a name=\"hpo-HP.580000629\"> </a></td><td>Periorbital fullness</td></tr><tr><td style=\"white-space:nowrap\">HP:0000178<a name=\"hpo-HP.580000178\"> </a></td><td>Abnormality of lower lip</td></tr><tr><td style=\"white-space:nowrap\">HP:0000168<a name=\"hpo-HP.580000168\"> </a></td><td>Abnormality of the gingiva</td></tr><tr><td style=\"white-space:nowrap\">HP:0001022<a name=\"hpo-HP.580001022\"> </a></td><td>Albinism</td></tr><tr><td style=\"white-space:nowrap\">HP:0000177<a name=\"hpo-HP.580000177\"> </a></td><td>Abnormality of upper lip</td></tr><tr><td style=\"white-space:nowrap\">HP:0001337<a name=\"hpo-HP.580001337\"> </a></td><td>Tremor</td></tr><tr><td style=\"white-space:nowrap\">HP:0002135<a name=\"hpo-HP.580002135\"> </a></td><td>Basal ganglia calcification</td></tr><tr><td style=\"white-space:nowrap\">HP:0002352<a name=\"hpo-HP.580002352\"> </a></td><td>Leukoencephalopathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0002514<a name=\"hpo-HP.580002514\"> </a></td><td>Cerebral calcification</td></tr><tr><td style=\"white-space:nowrap\">HP:0010576<a name=\"hpo-HP.580010576\"> </a></td><td>Intracranial cystic lesion</td></tr><tr><td style=\"white-space:nowrap\">HP:0001622<a name=\"hpo-HP.580001622\"> </a></td><td>Premature birth</td></tr><tr><td style=\"white-space:nowrap\">HP:0002415<a name=\"hpo-HP.580002415\"> </a></td><td>Leukodystrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0001320<a name=\"hpo-HP.580001320\"> </a></td><td>Cerebellar vermis hypoplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001773<a name=\"hpo-HP.580001773\"> </a></td><td>Short foot</td></tr><tr><td style=\"white-space:nowrap\">HP:0002750<a name=\"hpo-HP.580002750\"> </a></td><td>Delayed skeletal maturation</td></tr><tr><td style=\"white-space:nowrap\">HP:0004415<a name=\"hpo-HP.580004415\"> </a></td><td>Pulmonary artery stenosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0012741<a name=\"hpo-HP.580012741\"> </a></td><td>Unilateral cryptorchidism</td></tr><tr><td style=\"white-space:nowrap\">HP:0000036<a name=\"hpo-HP.580000036\"> </a></td><td>Abnormality of the penis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002408<a name=\"hpo-HP.580002408\"> </a></td><td>Cerebral arteriovenous malformation</td></tr><tr><td style=\"white-space:nowrap\">HP:0007457<a name=\"hpo-HP.580007457\"> </a></td><td>Prominent veins on trunk</td></tr><tr><td style=\"white-space:nowrap\">HP:0000378<a name=\"hpo-HP.580000378\"> </a></td><td>Cupped ear</td></tr><tr><td style=\"white-space:nowrap\">HP:0000396<a name=\"hpo-HP.580000396\"> </a></td><td>Overfolded helix</td></tr><tr><td style=\"white-space:nowrap\">HP:0000035<a name=\"hpo-HP.580000035\"> </a></td><td>Abnormal testis morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0009895<a name=\"hpo-HP.580009895\"> </a></td><td>Abnormality of the crus of the helix</td></tr><tr><td style=\"white-space:nowrap\">HP:0000034<a name=\"hpo-HP.580000034\"> </a></td><td>Hydrocele testis</td></tr><tr><td style=\"white-space:nowrap\">HP:0000722<a name=\"hpo-HP.580000722\"> </a></td><td>Obsessive-compulsive behavior</td></tr><tr><td style=\"white-space:nowrap\">HP:0000845<a name=\"hpo-HP.580000845\"> </a></td><td>Growth hormone excess</td></tr><tr><td style=\"white-space:nowrap\">HP:0100829<a name=\"hpo-HP.580100829\"> </a></td><td>Galactorrhea</td></tr><tr><td style=\"white-space:nowrap\">HP:0001578<a name=\"hpo-HP.580001578\"> </a></td><td>Increased circulating cortisol level</td></tr><tr><td style=\"white-space:nowrap\">HP:0000786<a name=\"hpo-HP.580000786\"> </a></td><td>Primary amenorrhea</td></tr><tr><td style=\"white-space:nowrap\">HP:0001701<a name=\"hpo-HP.580001701\"> </a></td><td>Pericarditis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002076<a name=\"hpo-HP.580002076\"> </a></td><td>Migraine</td></tr><tr><td style=\"white-space:nowrap\">HP:0004755<a name=\"hpo-HP.580004755\"> </a></td><td>Supraventricular tachycardia</td></tr><tr><td style=\"white-space:nowrap\">HP:0010522<a name=\"hpo-HP.580010522\"> </a></td><td>Dyslexia</td></tr><tr><td style=\"white-space:nowrap\">HP:0004313<a name=\"hpo-HP.580004313\"> </a></td><td>Decreased circulating antibody level</td></tr><tr><td style=\"white-space:nowrap\">HP:0000011<a name=\"hpo-HP.580000011\"> </a></td><td>Neurogenic bladder</td></tr><tr><td style=\"white-space:nowrap\">HP:0000641<a name=\"hpo-HP.580000641\"> </a></td><td>Dysmetric saccades</td></tr><tr><td style=\"white-space:nowrap\">HP:0007772<a name=\"hpo-HP.580007772\"> </a></td><td>Impaired smooth pursuit</td></tr><tr><td style=\"white-space:nowrap\">HP:0001583<a name=\"hpo-HP.580001583\"> </a></td><td>Rotary nystagmus</td></tr><tr><td style=\"white-space:nowrap\">HP:0010544<a name=\"hpo-HP.580010544\"> </a></td><td>Vertical nystagmus</td></tr><tr><td style=\"white-space:nowrap\">HP:0012735<a name=\"hpo-HP.580012735\"> </a></td><td>Cough</td></tr><tr><td style=\"white-space:nowrap\">HP:0002075<a name=\"hpo-HP.580002075\"> </a></td><td>Dysdiadochokinesis</td></tr><tr><td style=\"white-space:nowrap\">HP:0007256<a name=\"hpo-HP.580007256\"> </a></td><td>Abnormal pyramidal sign</td></tr><tr><td style=\"white-space:nowrap\">HP:0001257<a name=\"hpo-HP.580001257\"> </a></td><td>Spasticity</td></tr><tr><td style=\"white-space:nowrap\">HP:0002321<a name=\"hpo-HP.580002321\"> </a></td><td>Vertigo</td></tr><tr><td style=\"white-space:nowrap\">HP:0002384<a name=\"hpo-HP.580002384\"> </a></td><td>Focal impaired awareness seizure</td></tr><tr><td style=\"white-space:nowrap\">HP:0011376<a name=\"hpo-HP.580011376\"> </a></td><td>Morphological abnormality of the vestibule of the inner ear</td></tr><tr><td style=\"white-space:nowrap\">HP:0002326<a name=\"hpo-HP.580002326\"> </a></td><td>Transient ischemic attack</td></tr><tr><td style=\"white-space:nowrap\">HP:0005584<a name=\"hpo-HP.580005584\"> </a></td><td>Renal cell carcinoma</td></tr><tr><td style=\"white-space:nowrap\">HP:0003124<a name=\"hpo-HP.580003124\"> </a></td><td>Hypercholesterolemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0003002<a name=\"hpo-HP.580003002\"> </a></td><td>Breast carcinoma</td></tr><tr><td style=\"white-space:nowrap\">HP:0004953<a name=\"hpo-HP.580004953\"> </a></td><td>obsolete Dilatation of abdominal aorta</td></tr><tr><td style=\"white-space:nowrap\">HP:0004944<a name=\"hpo-HP.580004944\"> </a></td><td>Dilatation of the cerebral artery</td></tr><tr><td style=\"white-space:nowrap\">HP:0000100<a name=\"hpo-HP.580000100\"> </a></td><td>Nephrotic syndrome</td></tr><tr><td style=\"white-space:nowrap\">HP:0002783<a name=\"hpo-HP.580002783\"> </a></td><td>Recurrent lower respiratory tract infections</td></tr><tr><td style=\"white-space:nowrap\">HP:0003470<a name=\"hpo-HP.580003470\"> </a></td><td>Paralysis</td></tr><tr><td style=\"white-space:nowrap\">HP:0006597<a name=\"hpo-HP.580006597\"> </a></td><td>Diaphragmatic paralysis</td></tr><tr><td style=\"white-space:nowrap\">HP:0008151<a name=\"hpo-HP.580008151\"> </a></td><td>Prolonged prothrombin time</td></tr><tr><td style=\"white-space:nowrap\">HP:0010628<a name=\"hpo-HP.580010628\"> </a></td><td>Facial palsy</td></tr><tr><td style=\"white-space:nowrap\">HP:0011892<a name=\"hpo-HP.580011892\"> </a></td><td>Low levels of vitamin K</td></tr><tr><td style=\"white-space:nowrap\">HP:0001075<a name=\"hpo-HP.580001075\"> </a></td><td>Atrophic scars</td></tr><tr><td style=\"white-space:nowrap\">HP:0001816<a name=\"hpo-HP.580001816\"> </a></td><td>Thin nail</td></tr><tr><td style=\"white-space:nowrap\">HP:0002216<a name=\"hpo-HP.580002216\"> </a></td><td>Premature graying of hair</td></tr><tr><td style=\"white-space:nowrap\">HP:0003401<a name=\"hpo-HP.580003401\"> </a></td><td>Paresthesia</td></tr><tr><td style=\"white-space:nowrap\">HP:0100134<a name=\"hpo-HP.580100134\"> </a></td><td>Abnormality of the axillary hair</td></tr><tr><td style=\"white-space:nowrap\">HP:0100797<a name=\"hpo-HP.580100797\"> </a></td><td>Toenail dysplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0010461<a name=\"hpo-HP.580010461\"> </a></td><td>Abnormality of the male genitalia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000044<a name=\"hpo-HP.580000044\"> </a></td><td>Hypogonadotropic hypogonadism</td></tr><tr><td style=\"white-space:nowrap\">HP:0100568<a name=\"hpo-HP.580100568\"> </a></td><td>Neoplasm of the endocrine system</td></tr><tr><td style=\"white-space:nowrap\">HP:0001646<a name=\"hpo-HP.580001646\"> </a></td><td>Abnormal aortic valve morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0000813<a name=\"hpo-HP.580000813\"> </a></td><td>Bicornuate uterus</td></tr><tr><td style=\"white-space:nowrap\">HP:0004380<a name=\"hpo-HP.580004380\"> </a></td><td>Aortic valve calcification</td></tr><tr><td style=\"white-space:nowrap\">HP:0001650<a name=\"hpo-HP.580001650\"> </a></td><td>Aortic valve stenosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0000073<a name=\"hpo-HP.580000073\"> </a></td><td>Ureteral duplication</td></tr><tr><td style=\"white-space:nowrap\">HP:0100651<a name=\"hpo-HP.580100651\"> </a></td><td>Type I diabetes mellitus</td></tr><tr><td style=\"white-space:nowrap\">HP:0000819<a name=\"hpo-HP.580000819\"> </a></td><td>Diabetes mellitus</td></tr><tr><td style=\"white-space:nowrap\">HP:0000573<a name=\"hpo-HP.580000573\"> </a></td><td>Retinal hemorrhage</td></tr><tr><td style=\"white-space:nowrap\">HP:0005264<a name=\"hpo-HP.580005264\"> </a></td><td>Abnormality of the gallbladder</td></tr><tr><td style=\"white-space:nowrap\">HP:0000475<a name=\"hpo-HP.580000475\"> </a></td><td>Broad neck</td></tr><tr><td style=\"white-space:nowrap\">HP:0000089<a name=\"hpo-HP.580000089\"> </a></td><td>Renal hypoplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000921<a name=\"hpo-HP.580000921\"> </a></td><td>Missing ribs</td></tr><tr><td style=\"white-space:nowrap\">HP:0001789<a name=\"hpo-HP.580001789\"> </a></td><td>Hydrops fetalis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002089<a name=\"hpo-HP.580002089\"> </a></td><td>Pulmonary hypoplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0003422<a name=\"hpo-HP.580003422\"> </a></td><td>Vertebral segmentation defect</td></tr><tr><td style=\"white-space:nowrap\">HP:0002323<a name=\"hpo-HP.580002323\"> </a></td><td>Anencephaly</td></tr><tr><td style=\"white-space:nowrap\">HP:0000341<a name=\"hpo-HP.580000341\"> </a></td><td>Narrow forehead</td></tr><tr><td style=\"white-space:nowrap\">HP:0002869<a name=\"hpo-HP.580002869\"> </a></td><td>Flared iliac wings</td></tr><tr><td style=\"white-space:nowrap\">HP:0003100<a name=\"hpo-HP.580003100\"> </a></td><td>Slender long bone</td></tr><tr><td style=\"white-space:nowrap\">HP:0003275<a name=\"hpo-HP.580003275\"> </a></td><td>Narrow pelvis bone</td></tr><tr><td style=\"white-space:nowrap\">HP:0009891<a name=\"hpo-HP.580009891\"> </a></td><td>Underdeveloped supraorbital ridges</td></tr><tr><td style=\"white-space:nowrap\">HP:0011039<a name=\"hpo-HP.580011039\"> </a></td><td>Abnormality of the helix</td></tr><tr><td style=\"white-space:nowrap\">HP:0008572<a name=\"hpo-HP.580008572\"> </a></td><td>External ear malformation</td></tr><tr><td style=\"white-space:nowrap\">HP:0009738<a name=\"hpo-HP.580009738\"> </a></td><td>Abnormality of the antihelix</td></tr><tr><td style=\"white-space:nowrap\">HP:0011328<a name=\"hpo-HP.580011328\"> </a></td><td>Abnormality of fontanelles</td></tr><tr><td style=\"white-space:nowrap\">HP:0012155<a name=\"hpo-HP.580012155\"> </a></td><td>Decreased corneal sensation</td></tr><tr><td style=\"white-space:nowrap\">HP:0004602<a name=\"hpo-HP.580004602\"> </a></td><td>Cervical C2/C3 vertebral fusion</td></tr><tr><td style=\"white-space:nowrap\">HP:0002997<a name=\"hpo-HP.580002997\"> </a></td><td>Abnormality of the ulna</td></tr><tr><td style=\"white-space:nowrap\">HP:0009777<a name=\"hpo-HP.580009777\"> </a></td><td>Absent thumb</td></tr><tr><td style=\"white-space:nowrap\">HP:0002893<a name=\"hpo-HP.580002893\"> </a></td><td>Pituitary adenoma</td></tr><tr><td style=\"white-space:nowrap\">HP:0040278<a name=\"hpo-HP.580040278\"> </a></td><td>Prolactinoma</td></tr><tr><td style=\"white-space:nowrap\">HP:0001555<a name=\"hpo-HP.580001555\"> </a></td><td>Asymmetry of the thorax</td></tr><tr><td style=\"white-space:nowrap\">HP:0000902<a name=\"hpo-HP.580000902\"> </a></td><td>Rib fusion</td></tr><tr><td style=\"white-space:nowrap\">HP:0002164<a name=\"hpo-HP.580002164\"> </a></td><td>Nail dysplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0011314<a name=\"hpo-HP.580011314\"> </a></td><td>Abnormality of long bone morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0002867<a name=\"hpo-HP.580002867\"> </a></td><td>Abnormality of the ilium</td></tr><tr><td style=\"white-space:nowrap\">HP:0000774<a name=\"hpo-HP.580000774\"> </a></td><td>Narrow chest</td></tr><tr><td style=\"white-space:nowrap\">HP:0006482<a name=\"hpo-HP.580006482\"> </a></td><td>Abnormality of dental morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0004383<a name=\"hpo-HP.580004383\"> </a></td><td>Hypoplastic left heart</td></tr><tr><td style=\"white-space:nowrap\">HP:0002015<a name=\"hpo-HP.580002015\"> </a></td><td>Dysphagia</td></tr><tr><td style=\"white-space:nowrap\">HP:0500093<a name=\"hpo-HP.580500093\"> </a></td><td>Food allergy</td></tr><tr><td style=\"white-space:nowrap\">HP:0001519<a name=\"hpo-HP.580001519\"> </a></td><td>Disproportionate tall stature</td></tr><tr><td style=\"white-space:nowrap\">HP:0003179<a name=\"hpo-HP.580003179\"> </a></td><td>Protrusio acetabuli</td></tr><tr><td style=\"white-space:nowrap\">HP:0007385<a name=\"hpo-HP.580007385\"> </a></td><td>Aplasia cutis congenita of scalp</td></tr><tr><td style=\"white-space:nowrap\">HP:0000716<a name=\"hpo-HP.580000716\"> </a></td><td>Depressivity</td></tr><tr><td style=\"white-space:nowrap\">HP:0012583<a name=\"hpo-HP.580012583\"> </a></td><td>Unilateral renal hypoplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000618<a name=\"hpo-HP.580000618\"> </a></td><td>Blindness</td></tr><tr><td style=\"white-space:nowrap\">HP:0001004<a name=\"hpo-HP.580001004\"> </a></td><td>Lymphedema</td></tr><tr><td style=\"white-space:nowrap\">HP:0002652<a name=\"hpo-HP.580002652\"> </a></td><td>Skeletal dysplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0012520<a name=\"hpo-HP.580012520\"> </a></td><td>Perivascular spaces</td></tr><tr><td style=\"white-space:nowrap\">HP:0005293<a name=\"hpo-HP.580005293\"> </a></td><td>Venous insufficiency</td></tr><tr><td style=\"white-space:nowrap\">HP:0012432<a name=\"hpo-HP.580012432\"> </a></td><td>Chronic fatigue</td></tr><tr><td style=\"white-space:nowrap\">HP:0002578<a name=\"hpo-HP.580002578\"> </a></td><td>Gastroparesis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001658<a name=\"hpo-HP.580001658\"> </a></td><td>Myocardial infarction</td></tr><tr><td style=\"white-space:nowrap\">HP:0001802<a name=\"hpo-HP.580001802\"> </a></td><td>Absent toenail</td></tr><tr><td style=\"white-space:nowrap\">HP:0001821<a name=\"hpo-HP.580001821\"> </a></td><td>Broad nail</td></tr><tr><td style=\"white-space:nowrap\">HP:0000807<a name=\"hpo-HP.580000807\"> </a></td><td>Glandular hypospadias</td></tr><tr><td style=\"white-space:nowrap\">HP:0100582<a name=\"hpo-HP.580100582\"> </a></td><td>Nasal polyposis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002653<a name=\"hpo-HP.580002653\"> </a></td><td>Bone pain</td></tr><tr><td style=\"white-space:nowrap\">HP:0001073<a name=\"hpo-HP.580001073\"> </a></td><td>Cigarette-paper scars</td></tr><tr><td style=\"white-space:nowrap\">HP:0031913<a name=\"hpo-HP.580031913\"> </a></td><td>Rhombencephalosynapsis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002617<a name=\"hpo-HP.580002617\"> </a></td><td>Dilatation</td></tr><tr><td style=\"white-space:nowrap\">HP:0005107<a name=\"hpo-HP.580005107\"> </a></td><td>Abnormal sacrum morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0002025<a name=\"hpo-HP.580002025\"> </a></td><td>Anal stenosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0009099<a name=\"hpo-HP.580009099\"> </a></td><td>Median cleft palate</td></tr><tr><td style=\"white-space:nowrap\">HP:0003212<a name=\"hpo-HP.580003212\"> </a></td><td>Increased circulating IgE level</td></tr><tr><td style=\"white-space:nowrap\">HP:0001319<a name=\"hpo-HP.580001319\"> </a></td><td>Neonatal hypotonia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002659<a name=\"hpo-HP.580002659\"> </a></td><td>Increased susceptibility to fractures</td></tr><tr><td style=\"white-space:nowrap\">HP:0025246<a name=\"hpo-HP.580025246\"> </a></td><td>Trichilemmal cyst</td></tr><tr><td style=\"white-space:nowrap\">HP:0002107<a name=\"hpo-HP.580002107\"> </a></td><td>Pneumothorax</td></tr><tr><td style=\"white-space:nowrap\">HP:0000107<a name=\"hpo-HP.580000107\"> </a></td><td>Renal cyst</td></tr><tr><td style=\"white-space:nowrap\">HP:0001025<a name=\"hpo-HP.580001025\"> </a></td><td>Urticaria</td></tr><tr><td style=\"white-space:nowrap\">HP:0002204<a name=\"hpo-HP.580002204\"> </a></td><td>Pulmonary embolism</td></tr><tr><td style=\"white-space:nowrap\">HP:0001058<a name=\"hpo-HP.580001058\"> </a></td><td>Poor wound healing</td></tr><tr><td style=\"white-space:nowrap\">HP:0003010<a name=\"hpo-HP.580003010\"> </a></td><td>Prolonged bleeding time</td></tr><tr><td style=\"white-space:nowrap\">HP:0100502<a name=\"hpo-HP.580100502\"> </a></td><td>Vitamin B12 deficiency</td></tr><tr><td style=\"white-space:nowrap\">HP:0100510<a name=\"hpo-HP.580100510\"> </a></td><td>Low levels of vitamin C</td></tr><tr><td style=\"white-space:nowrap\">HP:0030976<a name=\"hpo-HP.580030976\"> </a></td><td>Abnormal factor VIII activity</td></tr><tr><td style=\"white-space:nowrap\">HP:0100789<a name=\"hpo-HP.580100789\"> </a></td><td>Torus palatinus</td></tr><tr><td style=\"white-space:nowrap\">HP:0000108<a name=\"hpo-HP.580000108\"> </a></td><td>Renal corticomedullary cysts</td></tr><tr><td style=\"white-space:nowrap\">HP:0000072<a name=\"hpo-HP.580000072\"> </a></td><td>Hydroureter</td></tr><tr><td style=\"white-space:nowrap\">HP:0000019<a name=\"hpo-HP.580000019\"> </a></td><td>Urinary hesitancy</td></tr><tr><td style=\"white-space:nowrap\">HP:0100771<a name=\"hpo-HP.580100771\"> </a></td><td>Hypoperistalsis</td></tr><tr><td style=\"white-space:nowrap\">HP:0000021<a name=\"hpo-HP.580000021\"> </a></td><td>Megacystis</td></tr><tr><td style=\"white-space:nowrap\">HP:0004388<a name=\"hpo-HP.580004388\"> </a></td><td>Microcolon</td></tr><tr><td style=\"white-space:nowrap\">HP:0005247<a name=\"hpo-HP.580005247\"> </a></td><td>Hypoplasia of the abdominal wall musculature</td></tr><tr><td style=\"white-space:nowrap\">HP:0004794<a name=\"hpo-HP.580004794\"> </a></td><td>Malrotation of small bowel</td></tr><tr><td style=\"white-space:nowrap\">HP:0000045<a name=\"hpo-HP.580000045\"> </a></td><td>Abnormality of the scrotum</td></tr><tr><td style=\"white-space:nowrap\">HP:0002236<a name=\"hpo-HP.580002236\"> </a></td><td>Frontal upsweep of hair</td></tr><tr><td style=\"white-space:nowrap\">HP:0000212<a name=\"hpo-HP.580000212\"> </a></td><td>Gingival overgrowth</td></tr><tr><td style=\"white-space:nowrap\">HP:0001808<a name=\"hpo-HP.580001808\"> </a></td><td>Fragile nails</td></tr><tr><td style=\"white-space:nowrap\">HP:0000225<a name=\"hpo-HP.580000225\"> </a></td><td>Gingival bleeding</td></tr><tr><td style=\"white-space:nowrap\">HP:0006009<a name=\"hpo-HP.580006009\"> </a></td><td>Broad phalanx</td></tr><tr><td style=\"white-space:nowrap\">HP:0001837<a name=\"hpo-HP.580001837\"> </a></td><td>Broad toe</td></tr><tr><td style=\"white-space:nowrap\">HP:0001946<a name=\"hpo-HP.580001946\"> </a></td><td>Ketosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002490<a name=\"hpo-HP.580002490\"> </a></td><td>Increased CSF lactate</td></tr><tr><td style=\"white-space:nowrap\">HP:0002922<a name=\"hpo-HP.580002922\"> </a></td><td>Increased CSF protein</td></tr><tr><td style=\"white-space:nowrap\">HP:0003128<a name=\"hpo-HP.580003128\"> </a></td><td>Lactic acidosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0003111<a name=\"hpo-HP.580003111\"> </a></td><td>Abnormal blood ion concentration</td></tr><tr><td style=\"white-space:nowrap\">HP:0032234<a name=\"hpo-HP.580032234\"> </a></td><td>Increased circulating creatine kinase MM isoform</td></tr><tr><td style=\"white-space:nowrap\">HP:0003348<a name=\"hpo-HP.580003348\"> </a></td><td>Hyperalaninemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0008347<a name=\"hpo-HP.580008347\"> </a></td><td>Decreased activity of mitochondrial complex IV</td></tr><tr><td style=\"white-space:nowrap\">HP:0000326<a name=\"hpo-HP.580000326\"> </a></td><td>Abnormality of the maxilla</td></tr><tr><td style=\"white-space:nowrap\">HP:0010758<a name=\"hpo-HP.580010758\"> </a></td><td>Abnormality of the premaxilla</td></tr><tr><td style=\"white-space:nowrap\">HP:0005681<a name=\"hpo-HP.580005681\"> </a></td><td>Juvenile rheumatoid arthritis</td></tr><tr><td style=\"white-space:nowrap\">HP:0000514<a name=\"hpo-HP.580000514\"> </a></td><td>Slow saccadic eye movements</td></tr><tr><td style=\"white-space:nowrap\">HP:0002788<a name=\"hpo-HP.580002788\"> </a></td><td>Recurrent upper respiratory tract infections</td></tr><tr><td style=\"white-space:nowrap\">HP:0003396<a name=\"hpo-HP.580003396\"> </a></td><td>Syringomyelia</td></tr><tr><td style=\"white-space:nowrap\">HP:0003011<a name=\"hpo-HP.580003011\"> </a></td><td>Abnormality of the musculature</td></tr><tr><td style=\"white-space:nowrap\">HP:0002098<a name=\"hpo-HP.580002098\"> </a></td><td>Respiratory distress</td></tr><tr><td style=\"white-space:nowrap\">HP:0002018<a name=\"hpo-HP.580002018\"> </a></td><td>Nausea</td></tr><tr><td style=\"white-space:nowrap\">HP:0002014<a name=\"hpo-HP.580002014\"> </a></td><td>Diarrhea</td></tr><tr><td style=\"white-space:nowrap\">HP:0025168<a name=\"hpo-HP.580025168\"> </a></td><td>Left ventricular diastolic dysfunction</td></tr><tr><td style=\"white-space:nowrap\">HP:0001679<a name=\"hpo-HP.580001679\"> </a></td><td>Abnormal aortic morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0000159<a name=\"hpo-HP.580000159\"> </a></td><td>Abnormal lip morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0011338<a name=\"hpo-HP.580011338\"> </a></td><td>Abnormality of mouth shape</td></tr><tr><td style=\"white-space:nowrap\">HP:0000478<a name=\"hpo-HP.580000478\"> </a></td><td>Abnormality of the eye</td></tr><tr><td style=\"white-space:nowrap\">HP:0000154<a name=\"hpo-HP.580000154\"> </a></td><td>Wide mouth</td></tr><tr><td style=\"white-space:nowrap\">HP:0001513<a name=\"hpo-HP.580001513\"> </a></td><td>Obesity</td></tr><tr><td style=\"white-space:nowrap\">HP:0002475<a name=\"hpo-HP.580002475\"> </a></td><td>Myelomeningocele</td></tr><tr><td style=\"white-space:nowrap\">HP:0003765<a name=\"hpo-HP.580003765\"> </a></td><td>Psoriasiform dermatitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0010289<a name=\"hpo-HP.580010289\"> </a></td><td>Cleft of alveolar ridge of maxilla</td></tr><tr><td style=\"white-space:nowrap\">HP:0003908<a name=\"hpo-HP.580003908\"> </a></td><td>Corner fracture of metaphysis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002190<a name=\"hpo-HP.580002190\"> </a></td><td>Choroid plexus cyst</td></tr><tr><td style=\"white-space:nowrap\">HP:0004370<a name=\"hpo-HP.580004370\"> </a></td><td>Abnormality of temperature regulation</td></tr><tr><td style=\"white-space:nowrap\">HP:0011611<a name=\"hpo-HP.580011611\"> </a></td><td>Interrupted aortic arch</td></tr><tr><td style=\"white-space:nowrap\">HP:0000737<a name=\"hpo-HP.580000737\"> </a></td><td>Irritability</td></tr><tr><td style=\"white-space:nowrap\">HP:0001344<a name=\"hpo-HP.580001344\"> </a></td><td>Absent speech</td></tr><tr><td style=\"white-space:nowrap\">HP:0002376<a name=\"hpo-HP.580002376\"> </a></td><td>Developmental regression</td></tr><tr><td style=\"white-space:nowrap\">HP:0002140<a name=\"hpo-HP.580002140\"> </a></td><td>Ischemic stroke</td></tr><tr><td style=\"white-space:nowrap\">HP:0001287<a name=\"hpo-HP.580001287\"> </a></td><td>Meningitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002721<a name=\"hpo-HP.580002721\"> </a></td><td>Immunodeficiency</td></tr><tr><td style=\"white-space:nowrap\">HP:0000041<a name=\"hpo-HP.580000041\"> </a></td><td>Chordee</td></tr><tr><td style=\"white-space:nowrap\">HP:0012854<a name=\"hpo-HP.580012854\"> </a></td><td>Midshaft hypospadias</td></tr><tr><td style=\"white-space:nowrap\">HP:0000808<a name=\"hpo-HP.580000808\"> </a></td><td>Penoscrotal hypospadias</td></tr><tr><td style=\"white-space:nowrap\">HP:0000048<a name=\"hpo-HP.580000048\"> </a></td><td>Bifid scrotum</td></tr><tr><td style=\"white-space:nowrap\">HP:0001047<a name=\"hpo-HP.580001047\"> </a></td><td>Atopic dermatitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001621<a name=\"hpo-HP.580001621\"> </a></td><td>Weak voice</td></tr><tr><td style=\"white-space:nowrap\">HP:0002372<a name=\"hpo-HP.580002372\"> </a></td><td>Normal interictal EEG</td></tr><tr><td style=\"white-space:nowrap\">HP:0012803<a name=\"hpo-HP.580012803\"> </a></td><td>Anisometropia</td></tr><tr><td style=\"white-space:nowrap\">HP:0011386<a name=\"hpo-HP.580011386\"> </a></td><td>Narrow internal auditory canal</td></tr><tr><td style=\"white-space:nowrap\">HP:0012714<a name=\"hpo-HP.580012714\"> </a></td><td>Severe hearing impairment</td></tr><tr><td style=\"white-space:nowrap\">HP:0006485<a name=\"hpo-HP.580006485\"> </a></td><td>Agenesis of incisor</td></tr><tr><td style=\"white-space:nowrap\">HP:0000787<a name=\"hpo-HP.580000787\"> </a></td><td>Nephrolithiasis</td></tr><tr><td style=\"white-space:nowrap\">HP:0011332<a name=\"hpo-HP.580011332\"> </a></td><td>Hemifacial hypoplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001909<a name=\"hpo-HP.580001909\"> </a></td><td>Leukemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0004808<a name=\"hpo-HP.580004808\"> </a></td><td>Acute myeloid leukemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0006495<a name=\"hpo-HP.580006495\"> </a></td><td>Aplasia/Hypoplasia of the ulna</td></tr><tr><td style=\"white-space:nowrap\">HP:0001180<a name=\"hpo-HP.580001180\"> </a></td><td>Hand oligodactyly</td></tr><tr><td style=\"white-space:nowrap\">HP:0002991<a name=\"hpo-HP.580002991\"> </a></td><td>Abnormality of fibula morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0001849<a name=\"hpo-HP.580001849\"> </a></td><td>Foot oligodactyly</td></tr><tr><td style=\"white-space:nowrap\">HP:0006507<a name=\"hpo-HP.580006507\"> </a></td><td>Aplasia/hypoplasia of the humerus</td></tr><tr><td style=\"white-space:nowrap\">HP:0005613<a name=\"hpo-HP.580005613\"> </a></td><td>Aplasia/hypoplasia of the femur</td></tr><tr><td style=\"white-space:nowrap\">HP:0006492<a name=\"hpo-HP.580006492\"> </a></td><td>Aplasia/Hypoplasia of the fibula</td></tr><tr><td style=\"white-space:nowrap\">HP:0000098<a name=\"hpo-HP.580000098\"> </a></td><td>Tall stature</td></tr><tr><td style=\"white-space:nowrap\">HP:0003311<a name=\"hpo-HP.580003311\"> </a></td><td>Hypoplasia of the odontoid process</td></tr><tr><td style=\"white-space:nowrap\">HP:0005752<a name=\"hpo-HP.580005752\"> </a></td><td>Flattened moderately deformed vertebrae</td></tr><tr><td style=\"white-space:nowrap\">HP:0030039<a name=\"hpo-HP.580030039\"> </a></td><td>Fused thoracic vertebrae</td></tr><tr><td style=\"white-space:nowrap\">HP:0003304<a name=\"hpo-HP.580003304\"> </a></td><td>Spondylolysis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001659<a name=\"hpo-HP.580001659\"> </a></td><td>Aortic regurgitation</td></tr><tr><td style=\"white-space:nowrap\">HP:0002984<a name=\"hpo-HP.580002984\"> </a></td><td>Hypoplasia of the radius</td></tr><tr><td style=\"white-space:nowrap\">HP:0009944<a name=\"hpo-HP.580009944\"> </a></td><td>Partial duplication of thumb phalanx</td></tr><tr><td style=\"white-space:nowrap\">HP:0005819<a name=\"hpo-HP.580005819\"> </a></td><td>Short middle phalanx of finger</td></tr><tr><td style=\"white-space:nowrap\">HP:0002110<a name=\"hpo-HP.580002110\"> </a></td><td>Bronchiectasis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001677<a name=\"hpo-HP.580001677\"> </a></td><td>Coronary artery atherosclerosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001737<a name=\"hpo-HP.580001737\"> </a></td><td>Pancreatic cysts</td></tr><tr><td style=\"white-space:nowrap\">HP:0005113<a name=\"hpo-HP.580005113\"> </a></td><td>Aortic arch aneurysm</td></tr><tr><td style=\"white-space:nowrap\">HP:0003022<a name=\"hpo-HP.580003022\"> </a></td><td>Hypoplasia of the ulna</td></tr><tr><td style=\"white-space:nowrap\">HP:0002205<a name=\"hpo-HP.580002205\"> </a></td><td>Recurrent respiratory infections</td></tr><tr><td style=\"white-space:nowrap\">HP:0001669<a name=\"hpo-HP.580001669\"> </a></td><td>Transposition of the great arteries</td></tr><tr><td style=\"white-space:nowrap\">HP:0001716<a name=\"hpo-HP.580001716\"> </a></td><td>Wolff-Parkinson-White syndrome</td></tr><tr><td style=\"white-space:nowrap\">HP:0002758<a name=\"hpo-HP.580002758\"> </a></td><td>Osteoarthritis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002037<a name=\"hpo-HP.580002037\"> </a></td><td>Inflammation of the large intestine</td></tr><tr><td style=\"white-space:nowrap\">HP:0009892<a name=\"hpo-HP.580009892\"> </a></td><td>Anotia</td></tr><tr><td style=\"white-space:nowrap\">HP:0011331<a name=\"hpo-HP.580011331\"> </a></td><td>Hemifacial atrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0009118<a name=\"hpo-HP.580009118\"> </a></td><td>Aplasia/Hypoplasia of the mandible</td></tr><tr><td style=\"white-space:nowrap\">HP:0009940<a name=\"hpo-HP.580009940\"> </a></td><td>Asymmetry of the mandible</td></tr><tr><td style=\"white-space:nowrap\">HP:0000682<a name=\"hpo-HP.580000682\"> </a></td><td>Abnormality of dental enamel</td></tr><tr><td style=\"white-space:nowrap\">HP:0009908<a name=\"hpo-HP.580009908\"> </a></td><td>Anterior creases of earlobe</td></tr><tr><td style=\"white-space:nowrap\">HP:0001541<a name=\"hpo-HP.580001541\"> </a></td><td>Ascites</td></tr><tr><td style=\"white-space:nowrap\">HP:0006687<a name=\"hpo-HP.580006687\"> </a></td><td>Aortic tortuosity</td></tr><tr><td style=\"white-space:nowrap\">HP:0010535<a name=\"hpo-HP.580010535\"> </a></td><td>Sleep apnea</td></tr><tr><td style=\"white-space:nowrap\">HP:0100633<a name=\"hpo-HP.580100633\"> </a></td><td>Esophagitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002105<a name=\"hpo-HP.580002105\"> </a></td><td>Hemoptysis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002613<a name=\"hpo-HP.580002613\"> </a></td><td>Biliary cirrhosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0004469<a name=\"hpo-HP.580004469\"> </a></td><td>Chronic bronchitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002720<a name=\"hpo-HP.580002720\"> </a></td><td>Decreased circulating IgA level</td></tr><tr><td style=\"white-space:nowrap\">HP:0002904<a name=\"hpo-HP.580002904\"> </a></td><td>Hyperbilirubinemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0003237<a name=\"hpo-HP.580003237\"> </a></td><td>Increased circulating IgG level</td></tr><tr><td style=\"white-space:nowrap\">HP:0003262<a name=\"hpo-HP.580003262\"> </a></td><td>Smooth muscle antibody positivity</td></tr><tr><td style=\"white-space:nowrap\">HP:0011227<a name=\"hpo-HP.580011227\"> </a></td><td>Elevated C-reactive protein level</td></tr><tr><td style=\"white-space:nowrap\">HP:0001852<a name=\"hpo-HP.580001852\"> </a></td><td>Sandal gap</td></tr><tr><td style=\"white-space:nowrap\">HP:0004381<a name=\"hpo-HP.580004381\"> </a></td><td>Supravalvular aortic stenosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0100700<a name=\"hpo-HP.580100700\"> </a></td><td>Abnormal arachnoid mater morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0002624<a name=\"hpo-HP.580002624\"> </a></td><td>Abnormal venous morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0002289<a name=\"hpo-HP.580002289\"> </a></td><td>Alopecia universalis</td></tr><tr><td style=\"white-space:nowrap\">HP:0009588<a name=\"hpo-HP.580009588\"> </a></td><td>Vestibular Schwannoma</td></tr><tr><td style=\"white-space:nowrap\">HP:0001648<a name=\"hpo-HP.580001648\"> </a></td><td>Cor pulmonale</td></tr><tr><td style=\"white-space:nowrap\">HP:0002091<a name=\"hpo-HP.580002091\"> </a></td><td>Restrictive ventilatory defect</td></tr><tr><td style=\"white-space:nowrap\">HP:0002092<a name=\"hpo-HP.580002092\"> </a></td><td>Pulmonary arterial hypertension</td></tr><tr><td style=\"white-space:nowrap\">HP:0002113<a name=\"hpo-HP.580002113\"> </a></td><td>Pulmonary infiltrates</td></tr><tr><td style=\"white-space:nowrap\">HP:0003138<a name=\"hpo-HP.580003138\"> </a></td><td>Increased blood urea nitrogen</td></tr><tr><td style=\"white-space:nowrap\">HP:0003259<a name=\"hpo-HP.580003259\"> </a></td><td>Elevated serum creatinine</td></tr><tr><td style=\"white-space:nowrap\">HP:0005180<a name=\"hpo-HP.580005180\"> </a></td><td>Tricuspid regurgitation</td></tr><tr><td style=\"white-space:nowrap\">HP:0012585<a name=\"hpo-HP.580012585\"> </a></td><td>Renal atrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0005133<a name=\"hpo-HP.580005133\"> </a></td><td>Right ventricular dilatation</td></tr><tr><td style=\"white-space:nowrap\">HP:0005575<a name=\"hpo-HP.580005575\"> </a></td><td>Hemolytic-uremic syndrome</td></tr><tr><td style=\"white-space:nowrap\">HP:0001697<a name=\"hpo-HP.580001697\"> </a></td><td>Abnormal pericardium morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0012486<a name=\"hpo-HP.580012486\"> </a></td><td>Myelitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002385<a name=\"hpo-HP.580002385\"> </a></td><td>Paraparesis</td></tr><tr><td style=\"white-space:nowrap\">HP:0006706<a name=\"hpo-HP.580006706\"> </a></td><td>Cystic liver disease</td></tr><tr><td style=\"white-space:nowrap\">HP:0010880<a name=\"hpo-HP.580010880\"> </a></td><td>Increased nuchal translucency</td></tr><tr><td style=\"white-space:nowrap\">HP:0000457<a name=\"hpo-HP.580000457\"> </a></td><td>Depressed nasal ridge</td></tr><tr><td style=\"white-space:nowrap\">HP:0002263<a name=\"hpo-HP.580002263\"> </a></td><td>Exaggerated cupid's bow</td></tr><tr><td style=\"white-space:nowrap\">HP:0002500<a name=\"hpo-HP.580002500\"> </a></td><td>Abnormality of the cerebral white matter</td></tr><tr><td style=\"white-space:nowrap\">HP:0002835<a name=\"hpo-HP.580002835\"> </a></td><td>Aspiration</td></tr><tr><td style=\"white-space:nowrap\">HP:0000600<a name=\"hpo-HP.580000600\"> </a></td><td>Abnormality of the pharynx</td></tr><tr><td style=\"white-space:nowrap\">HP:0004327<a name=\"hpo-HP.580004327\"> </a></td><td>Abnormal vitreous humor morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0004378<a name=\"hpo-HP.580004378\"> </a></td><td>Abnormality of the anus</td></tr><tr><td style=\"white-space:nowrap\">HP:0012374<a name=\"hpo-HP.580012374\"> </a></td><td>obsolete Abnormal globe morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0100768<a name=\"hpo-HP.580100768\"> </a></td><td>Choriocarcinoma</td></tr><tr><td style=\"white-space:nowrap\">HP:0030991<a name=\"hpo-HP.580030991\"> </a></td><td>Sclerosing cholangitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0006510<a name=\"hpo-HP.580006510\"> </a></td><td>Chronic pulmonary obstruction</td></tr><tr><td style=\"white-space:nowrap\">HP:0000710<a name=\"hpo-HP.580000710\"> </a></td><td>Hyperorality</td></tr><tr><td style=\"white-space:nowrap\">HP:0001270<a name=\"hpo-HP.580001270\"> </a></td><td>Motor delay</td></tr><tr><td style=\"white-space:nowrap\">HP:0001548<a name=\"hpo-HP.580001548\"> </a></td><td>Overgrowth</td></tr><tr><td style=\"white-space:nowrap\">HP:0002311<a name=\"hpo-HP.580002311\"> </a></td><td>Incoordination</td></tr><tr><td style=\"white-space:nowrap\">HP:0006288<a name=\"hpo-HP.580006288\"> </a></td><td>Advanced eruption of teeth</td></tr><tr><td style=\"white-space:nowrap\">HP:0006323<a name=\"hpo-HP.580006323\"> </a></td><td>Premature loss of primary teeth</td></tr><tr><td style=\"white-space:nowrap\">HP:0009890<a name=\"hpo-HP.580009890\"> </a></td><td>High anterior hairline</td></tr><tr><td style=\"white-space:nowrap\">HP:0100034<a name=\"hpo-HP.580100034\"> </a></td><td>Motor tics</td></tr><tr><td style=\"white-space:nowrap\">HP:0100035<a name=\"hpo-HP.580100035\"> </a></td><td>Phonic tics</td></tr><tr><td style=\"white-space:nowrap\">HP:0000348<a name=\"hpo-HP.580000348\"> </a></td><td>High forehead</td></tr><tr><td style=\"white-space:nowrap\">HP:0001520<a name=\"hpo-HP.580001520\"> </a></td><td>Large for gestational age</td></tr><tr><td style=\"white-space:nowrap\">HP:0001239<a name=\"hpo-HP.580001239\"> </a></td><td>Wrist flexion contracture</td></tr><tr><td style=\"white-space:nowrap\">HP:0007359<a name=\"hpo-HP.580007359\"> </a></td><td>Focal-onset seizure</td></tr><tr><td style=\"white-space:nowrap\">HP:0000430<a name=\"hpo-HP.580000430\"> </a></td><td>Underdeveloped nasal alae</td></tr><tr><td style=\"white-space:nowrap\">HP:0007400<a name=\"hpo-HP.580007400\"> </a></td><td>Irregular hyperpigmentation</td></tr><tr><td style=\"white-space:nowrap\">HP:0100495<a name=\"hpo-HP.580100495\"> </a></td><td>Mastocytosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0012378<a name=\"hpo-HP.580012378\"> </a></td><td>Fatigue</td></tr><tr><td style=\"white-space:nowrap\">HP:0002046<a name=\"hpo-HP.580002046\"> </a></td><td>Heat intolerance</td></tr><tr><td style=\"white-space:nowrap\">HP:0003270<a name=\"hpo-HP.580003270\"> </a></td><td>Abdominal distention</td></tr><tr><td style=\"white-space:nowrap\">HP:0002180<a name=\"hpo-HP.580002180\"> </a></td><td>Neurodegeneration</td></tr><tr><td style=\"white-space:nowrap\">HP:0003493<a name=\"hpo-HP.580003493\"> </a></td><td>Antinuclear antibody positivity</td></tr><tr><td style=\"white-space:nowrap\">HP:0030057<a name=\"hpo-HP.580030057\"> </a></td><td>Autoimmune antibody positivity</td></tr><tr><td style=\"white-space:nowrap\">HP:0006802<a name=\"hpo-HP.580006802\"> </a></td><td>Abnormal anterior horn cell morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0000064<a name=\"hpo-HP.580000064\"> </a></td><td>Hypoplastic labia minora</td></tr><tr><td style=\"white-space:nowrap\">HP:0000338<a name=\"hpo-HP.580000338\"> </a></td><td>Hypomimic face</td></tr><tr><td style=\"white-space:nowrap\">HP:0001642<a name=\"hpo-HP.580001642\"> </a></td><td>Pulmonic stenosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0011344<a name=\"hpo-HP.580011344\"> </a></td><td>Severe global developmental delay</td></tr><tr><td style=\"white-space:nowrap\">HP:0200007<a name=\"hpo-HP.580200007\"> </a></td><td>Abnormal size of the palpebral fissures</td></tr><tr><td style=\"white-space:nowrap\">HP:0004464<a name=\"hpo-HP.580004464\"> </a></td><td>Postauricular pit</td></tr><tr><td style=\"white-space:nowrap\">HP:0000130<a name=\"hpo-HP.580000130\"> </a></td><td>Abnormality of the uterus</td></tr><tr><td style=\"white-space:nowrap\">HP:0000137<a name=\"hpo-HP.580000137\"> </a></td><td>Abnormality of the ovary</td></tr><tr><td style=\"white-space:nowrap\">HP:0000142<a name=\"hpo-HP.580000142\"> </a></td><td>Abnormal vagina morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0000370<a name=\"hpo-HP.580000370\"> </a></td><td>Abnormality of the middle ear</td></tr><tr><td style=\"white-space:nowrap\">HP:0011787<a name=\"hpo-HP.580011787\"> </a></td><td>Central hypothyroidism</td></tr><tr><td style=\"white-space:nowrap\">HP:0000274<a name=\"hpo-HP.580000274\"> </a></td><td>Small face</td></tr><tr><td style=\"white-space:nowrap\">HP:0000446<a name=\"hpo-HP.580000446\"> </a></td><td>Narrow nasal bridge</td></tr><tr><td style=\"white-space:nowrap\">HP:0000622<a name=\"hpo-HP.580000622\"> </a></td><td>Blurred vision</td></tr><tr><td style=\"white-space:nowrap\">HP:0001245<a name=\"hpo-HP.580001245\"> </a></td><td>Small thenar eminence</td></tr><tr><td style=\"white-space:nowrap\">HP:0009601<a name=\"hpo-HP.580009601\"> </a></td><td>Aplasia/Hypoplasia of the thumb</td></tr><tr><td style=\"white-space:nowrap\">HP:0011343<a name=\"hpo-HP.580011343\"> </a></td><td>Moderate global developmental delay</td></tr><tr><td style=\"white-space:nowrap\">HP:0000419<a name=\"hpo-HP.580000419\"> </a></td><td>Abnormality of the nasal septum</td></tr><tr><td style=\"white-space:nowrap\">HP:0000502<a name=\"hpo-HP.580000502\"> </a></td><td>Abnormal conjunctiva morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0000591<a name=\"hpo-HP.580000591\"> </a></td><td>Abnormal sclera morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0000615<a name=\"hpo-HP.580000615\"> </a></td><td>Abnormal pupil morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0001163<a name=\"hpo-HP.580001163\"> </a></td><td>Abnormality of the metacarpal bones</td></tr><tr><td style=\"white-space:nowrap\">HP:0001832<a name=\"hpo-HP.580001832\"> </a></td><td>Abnormal metatarsal morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0001850<a name=\"hpo-HP.580001850\"> </a></td><td>Abnormality of the tarsal bones</td></tr><tr><td style=\"white-space:nowrap\">HP:0010490<a name=\"hpo-HP.580010490\"> </a></td><td>Abnormality of the palmar creases</td></tr><tr><td style=\"white-space:nowrap\">HP:0010881<a name=\"hpo-HP.580010881\"> </a></td><td>Abnormality of the umbilical cord</td></tr><tr><td style=\"white-space:nowrap\">HP:0009113<a name=\"hpo-HP.580009113\"> </a></td><td>Diaphragmatic weakness</td></tr><tr><td style=\"white-space:nowrap\">HP:0011664<a name=\"hpo-HP.580011664\"> </a></td><td>Left ventricular noncompaction cardiomyopathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0100240<a name=\"hpo-HP.580100240\"> </a></td><td>Synostosis of joints</td></tr><tr><td style=\"white-space:nowrap\">HP:0001838<a name=\"hpo-HP.580001838\"> </a></td><td>Rocker bottom foot</td></tr><tr><td style=\"white-space:nowrap\">HP:0003717<a name=\"hpo-HP.580003717\"> </a></td><td>Minimal subcutaneous fat</td></tr><tr><td style=\"white-space:nowrap\">HP:0001339<a name=\"hpo-HP.580001339\"> </a></td><td>Lissencephaly</td></tr><tr><td style=\"white-space:nowrap\">HP:0001591<a name=\"hpo-HP.580001591\"> </a></td><td>Bell-shaped thorax</td></tr><tr><td style=\"white-space:nowrap\">HP:0002655<a name=\"hpo-HP.580002655\"> </a></td><td>Spondyloepiphyseal dysplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002983<a name=\"hpo-HP.580002983\"> </a></td><td>Micromelia</td></tr><tr><td style=\"white-space:nowrap\">HP:0003016<a name=\"hpo-HP.580003016\"> </a></td><td>Metaphyseal widening</td></tr><tr><td style=\"white-space:nowrap\">HP:0009826<a name=\"hpo-HP.580009826\"> </a></td><td>Limb undergrowth</td></tr><tr><td style=\"white-space:nowrap\">HP:0004488<a name=\"hpo-HP.580004488\"> </a></td><td>Macrocephaly at birth</td></tr><tr><td style=\"white-space:nowrap\">HP:0001695<a name=\"hpo-HP.580001695\"> </a></td><td>Cardiac arrest</td></tr><tr><td style=\"white-space:nowrap\">HP:0001712<a name=\"hpo-HP.580001712\"> </a></td><td>Left ventricular hypertrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0100775<a name=\"hpo-HP.580100775\"> </a></td><td>Dural ectasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000846<a name=\"hpo-HP.580000846\"> </a></td><td>Adrenal insufficiency</td></tr><tr><td style=\"white-space:nowrap\">HP:0002925<a name=\"hpo-HP.580002925\"> </a></td><td>Increased thyroid-stimulating hormone level</td></tr><tr><td style=\"white-space:nowrap\">HP:0100646<a name=\"hpo-HP.580100646\"> </a></td><td>Thyroiditis</td></tr><tr><td style=\"white-space:nowrap\">HP:0000836<a name=\"hpo-HP.580000836\"> </a></td><td>Hyperthyroidism</td></tr><tr><td style=\"white-space:nowrap\">HP:0004414<a name=\"hpo-HP.580004414\"> </a></td><td>Abnormality of the pulmonary artery</td></tr><tr><td style=\"white-space:nowrap\">HP:0000465<a name=\"hpo-HP.580000465\"> </a></td><td>Webbed neck</td></tr><tr><td style=\"white-space:nowrap\">HP:0000723<a name=\"hpo-HP.580000723\"> </a></td><td>Restrictive behavior</td></tr><tr><td style=\"white-space:nowrap\">HP:0002253<a name=\"hpo-HP.580002253\"> </a></td><td>Colonic diverticula</td></tr><tr><td style=\"white-space:nowrap\">HP:0001310<a name=\"hpo-HP.580001310\"> </a></td><td>Dysmetria</td></tr><tr><td style=\"white-space:nowrap\">HP:0000093<a name=\"hpo-HP.580000093\"> </a></td><td>Proteinuria</td></tr><tr><td style=\"white-space:nowrap\">HP:0002907<a name=\"hpo-HP.580002907\"> </a></td><td>Microscopic hematuria</td></tr><tr><td style=\"white-space:nowrap\">HP:0003073<a name=\"hpo-HP.580003073\"> </a></td><td>Hypoalbuminemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0004315<a name=\"hpo-HP.580004315\"> </a></td><td>Decreased circulating IgG level</td></tr><tr><td style=\"white-space:nowrap\">HP:0000795<a name=\"hpo-HP.580000795\"> </a></td><td>Abnormality of the urethra</td></tr><tr><td style=\"white-space:nowrap\">HP:0001015<a name=\"hpo-HP.580001015\"> </a></td><td>Prominent superficial veins</td></tr><tr><td style=\"white-space:nowrap\">HP:0004691<a name=\"hpo-HP.580004691\"> </a></td><td>2-3 toe syndactyly</td></tr><tr><td style=\"white-space:nowrap\">HP:0005328<a name=\"hpo-HP.580005328\"> </a></td><td>Progeroid facial appearance</td></tr><tr><td style=\"white-space:nowrap\">HP:0005487<a name=\"hpo-HP.580005487\"> </a></td><td>Prominent metopic ridge</td></tr><tr><td style=\"white-space:nowrap\">HP:0007552<a name=\"hpo-HP.580007552\"> </a></td><td>Abnormal subcutaneous fat tissue distribution</td></tr><tr><td style=\"white-space:nowrap\">HP:0100678<a name=\"hpo-HP.580100678\"> </a></td><td>Premature skin wrinkling</td></tr><tr><td style=\"white-space:nowrap\">HP:0031137<a name=\"hpo-HP.580031137\"> </a></td><td>Storage in hepatocytes</td></tr><tr><td style=\"white-space:nowrap\">HP:0002521<a name=\"hpo-HP.580002521\"> </a></td><td>Hypsarrhythmia</td></tr><tr><td style=\"white-space:nowrap\">HP:0005390<a name=\"hpo-HP.580005390\"> </a></td><td>Recurrent opportunistic infections</td></tr><tr><td style=\"white-space:nowrap\">HP:0002716<a name=\"hpo-HP.580002716\"> </a></td><td>Lymphadenopathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0005379<a name=\"hpo-HP.580005379\"> </a></td><td>obsolete Severe T lymphocytopenia</td></tr><tr><td style=\"white-space:nowrap\">HP:0004432<a name=\"hpo-HP.580004432\"> </a></td><td>Agammaglobulinemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0006695<a name=\"hpo-HP.580006695\"> </a></td><td>Atrioventricular canal defect</td></tr><tr><td style=\"white-space:nowrap\">HP:0001733<a name=\"hpo-HP.580001733\"> </a></td><td>Pancreatitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002350<a name=\"hpo-HP.580002350\"> </a></td><td>Cerebellar cyst</td></tr><tr><td style=\"white-space:nowrap\">HP:0012110<a name=\"hpo-HP.580012110\"> </a></td><td>Hypoplasia of the pons</td></tr><tr><td style=\"white-space:nowrap\">HP:0001948<a name=\"hpo-HP.580001948\"> </a></td><td>Alkalosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0003113<a name=\"hpo-HP.580003113\"> </a></td><td>Hypochloremia</td></tr><tr><td style=\"white-space:nowrap\">HP:0003155<a name=\"hpo-HP.580003155\"> </a></td><td>Elevated alkaline phosphatase</td></tr><tr><td style=\"white-space:nowrap\">HP:0003542<a name=\"hpo-HP.580003542\"> </a></td><td>Increased serum pyruvate</td></tr><tr><td style=\"white-space:nowrap\">HP:0000421<a name=\"hpo-HP.580000421\"> </a></td><td>Epistaxis</td></tr><tr><td style=\"white-space:nowrap\">HP:0200136<a name=\"hpo-HP.580200136\"> </a></td><td>Oral-pharyngeal dysphagia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000805<a name=\"hpo-HP.580000805\"> </a></td><td>Enuresis</td></tr><tr><td style=\"white-space:nowrap\">HP:0005616<a name=\"hpo-HP.580005616\"> </a></td><td>Accelerated skeletal maturation</td></tr><tr><td style=\"white-space:nowrap\">HP:0002459<a name=\"hpo-HP.580002459\"> </a></td><td>obsolete Dysautonomia</td></tr><tr><td style=\"white-space:nowrap\">HP:0007302<a name=\"hpo-HP.580007302\"> </a></td><td>Bipolar affective disorder</td></tr><tr><td style=\"white-space:nowrap\">HP:0100602<a name=\"hpo-HP.580100602\"> </a></td><td>Preeclampsia</td></tr><tr><td style=\"white-space:nowrap\">HP:0100508<a name=\"hpo-HP.580100508\"> </a></td><td>Abnormality of vitamin metabolism</td></tr><tr><td style=\"white-space:nowrap\">HP:0001140<a name=\"hpo-HP.580001140\"> </a></td><td>Limbal dermoid</td></tr><tr><td style=\"white-space:nowrap\">HP:0000143<a name=\"hpo-HP.580000143\"> </a></td><td>Rectovaginal fistula</td></tr><tr><td style=\"white-space:nowrap\">HP:0001746<a name=\"hpo-HP.580001746\"> </a></td><td>Asplenia</td></tr><tr><td style=\"white-space:nowrap\">HP:0012715<a name=\"hpo-HP.580012715\"> </a></td><td>Profound hearing impairment</td></tr><tr><td style=\"white-space:nowrap\">HP:0001748<a name=\"hpo-HP.580001748\"> </a></td><td>Polysplenia</td></tr><tr><td style=\"white-space:nowrap\">HP:0003072<a name=\"hpo-HP.580003072\"> </a></td><td>Hypercalcemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002905<a name=\"hpo-HP.580002905\"> </a></td><td>Hyperphosphatemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002901<a name=\"hpo-HP.580002901\"> </a></td><td>Hypocalcemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001367<a name=\"hpo-HP.580001367\"> </a></td><td>Abnormal joint morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0010562<a name=\"hpo-HP.580010562\"> </a></td><td>Keloids</td></tr><tr><td style=\"white-space:nowrap\">HP:0004430<a name=\"hpo-HP.580004430\"> </a></td><td>Severe combined immunodeficiency</td></tr><tr><td style=\"white-space:nowrap\">HP:0000003<a name=\"hpo-HP.580000003\"> </a></td><td>Multicystic kidney dysplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0010980<a name=\"hpo-HP.580010980\"> </a></td><td>Hyperlipoproteinemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002155<a name=\"hpo-HP.580002155\"> </a></td><td>Hypertriglyceridemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000520<a name=\"hpo-HP.580000520\"> </a></td><td>Proptosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0000180<a name=\"hpo-HP.580000180\"> </a></td><td>Lobulated tongue</td></tr><tr><td style=\"white-space:nowrap\">HP:0005486<a name=\"hpo-HP.580005486\"> </a></td><td>Small fontanelle</td></tr><tr><td style=\"white-space:nowrap\">HP:0000891<a name=\"hpo-HP.580000891\"> </a></td><td>Cervical ribs</td></tr><tr><td style=\"white-space:nowrap\">HP:0002557<a name=\"hpo-HP.580002557\"> </a></td><td>Hypoplastic nipples</td></tr><tr><td style=\"white-space:nowrap\">HP:0009112<a name=\"hpo-HP.580009112\"> </a></td><td>Aplasia of the left hemidiaphragm</td></tr><tr><td style=\"white-space:nowrap\">HP:0001719<a name=\"hpo-HP.580001719\"> </a></td><td>Double outlet right ventricle</td></tr><tr><td style=\"white-space:nowrap\">HP:0001682<a name=\"hpo-HP.580001682\"> </a></td><td>Subvalvular aortic stenosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001667<a name=\"hpo-HP.580001667\"> </a></td><td>Right ventricular hypertrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0002101<a name=\"hpo-HP.580002101\"> </a></td><td>Abnormal lung lobation</td></tr><tr><td style=\"white-space:nowrap\">HP:0002202<a name=\"hpo-HP.580002202\"> </a></td><td>Pleural effusion</td></tr><tr><td style=\"white-space:nowrap\">HP:0002566<a name=\"hpo-HP.580002566\"> </a></td><td>Intestinal malrotation</td></tr><tr><td style=\"white-space:nowrap\">HP:0004510<a name=\"hpo-HP.580004510\"> </a></td><td>Pancreatic islet-cell hyperplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001747<a name=\"hpo-HP.580001747\"> </a></td><td>Accessory spleen</td></tr><tr><td style=\"white-space:nowrap\">HP:0002181<a name=\"hpo-HP.580002181\"> </a></td><td>Cerebral edema</td></tr><tr><td style=\"white-space:nowrap\">HP:0000967<a name=\"hpo-HP.580000967\"> </a></td><td>Petechiae</td></tr><tr><td style=\"white-space:nowrap\">HP:0009702<a name=\"hpo-HP.580009702\"> </a></td><td>Carpal synostosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0000927<a name=\"hpo-HP.580000927\"> </a></td><td>Abnormality of skeletal maturation</td></tr><tr><td style=\"white-space:nowrap\">HP:0004348<a name=\"hpo-HP.580004348\"> </a></td><td>Abnormality of bone mineral density</td></tr><tr><td style=\"white-space:nowrap\">HP:0003019<a name=\"hpo-HP.580003019\"> </a></td><td>Abnormality of the wrist</td></tr><tr><td style=\"white-space:nowrap\">HP:0003063<a name=\"hpo-HP.580003063\"> </a></td><td>Abnormality of the humerus</td></tr><tr><td style=\"white-space:nowrap\">HP:0001059<a name=\"hpo-HP.580001059\"> </a></td><td>Pterygium</td></tr><tr><td style=\"white-space:nowrap\">HP:0001528<a name=\"hpo-HP.580001528\"> </a></td><td>Hemihypertrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0011228<a name=\"hpo-HP.580011228\"> </a></td><td>Horizontal eyebrow</td></tr><tr><td style=\"white-space:nowrap\">HP:0000766<a name=\"hpo-HP.580000766\"> </a></td><td>Abnormality of the sternum</td></tr><tr><td style=\"white-space:nowrap\">HP:0001254<a name=\"hpo-HP.580001254\"> </a></td><td>Lethargy</td></tr><tr><td style=\"white-space:nowrap\">HP:0002360<a name=\"hpo-HP.580002360\"> </a></td><td>Sleep disturbance</td></tr><tr><td style=\"white-space:nowrap\">HP:0001063<a name=\"hpo-HP.580001063\"> </a></td><td>Acrocyanosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001769<a name=\"hpo-HP.580001769\"> </a></td><td>Broad foot</td></tr><tr><td style=\"white-space:nowrap\">HP:0010280<a name=\"hpo-HP.580010280\"> </a></td><td>Stomatitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001288<a name=\"hpo-HP.580001288\"> </a></td><td>Gait disturbance</td></tr><tr><td style=\"white-space:nowrap\">HP:0008330<a name=\"hpo-HP.580008330\"> </a></td><td>Reduced von Willebrand factor activity</td></tr><tr><td style=\"white-space:nowrap\">HP:0001954<a name=\"hpo-HP.580001954\"> </a></td><td>Recurrent fever</td></tr><tr><td style=\"white-space:nowrap\">HP:0004311<a name=\"hpo-HP.580004311\"> </a></td><td>Abnormal macrophage morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0012539<a name=\"hpo-HP.580012539\"> </a></td><td>Non-Hodgkin lymphoma</td></tr><tr><td style=\"white-space:nowrap\">HP:0002074<a name=\"hpo-HP.580002074\"> </a></td><td>Increased neuronal autofluorescent lipopigment</td></tr><tr><td style=\"white-space:nowrap\">HP:0002973<a name=\"hpo-HP.580002973\"> </a></td><td>Abnormality of the forearm</td></tr><tr><td style=\"white-space:nowrap\">HP:0003203<a name=\"hpo-HP.580003203\"> </a></td><td>Impaired oxidative burst</td></tr><tr><td style=\"white-space:nowrap\">HP:0003027<a name=\"hpo-HP.580003027\"> </a></td><td>Mesomelia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002754<a name=\"hpo-HP.580002754\"> </a></td><td>Osteomyelitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0004431<a name=\"hpo-HP.580004431\"> </a></td><td>Complement deficiency</td></tr><tr><td style=\"white-space:nowrap\">HP:0001258<a name=\"hpo-HP.580001258\"> </a></td><td>Spastic paraplegia</td></tr><tr><td style=\"white-space:nowrap\">HP:0012811<a name=\"hpo-HP.580012811\"> </a></td><td>Wide nasal ridge</td></tr><tr><td style=\"white-space:nowrap\">HP:0011832<a name=\"hpo-HP.580011832\"> </a></td><td>Narrow nasal tip</td></tr><tr><td style=\"white-space:nowrap\">HP:0000288<a name=\"hpo-HP.580000288\"> </a></td><td>Abnormality of the philtrum</td></tr><tr><td style=\"white-space:nowrap\">HP:0002357<a name=\"hpo-HP.580002357\"> </a></td><td>Dysphasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000871<a name=\"hpo-HP.580000871\"> </a></td><td>Panhypopituitarism</td></tr><tr><td style=\"white-space:nowrap\">HP:0000233<a name=\"hpo-HP.580000233\"> </a></td><td>Thin vermilion border</td></tr><tr><td style=\"white-space:nowrap\">HP:0003281<a name=\"hpo-HP.580003281\"> </a></td><td>Increased serum ferritin</td></tr><tr><td style=\"white-space:nowrap\">HP:0010752<a name=\"hpo-HP.580010752\"> </a></td><td>Cleft mandible</td></tr><tr><td style=\"white-space:nowrap\">HP:0000437<a name=\"hpo-HP.580000437\"> </a></td><td>Depressed nasal tip</td></tr><tr><td style=\"white-space:nowrap\">HP:0000453<a name=\"hpo-HP.580000453\"> </a></td><td>Choanal atresia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000863<a name=\"hpo-HP.580000863\"> </a></td><td>Central diabetes insipidus</td></tr><tr><td style=\"white-space:nowrap\">HP:0000058<a name=\"hpo-HP.580000058\"> </a></td><td>Abnormality of the labia</td></tr><tr><td style=\"white-space:nowrap\">HP:0007418<a name=\"hpo-HP.580007418\"> </a></td><td>Alopecia totalis</td></tr><tr><td style=\"white-space:nowrap\">HP:0100765<a name=\"hpo-HP.580100765\"> </a></td><td>Abnormality of the tonsils</td></tr><tr><td style=\"white-space:nowrap\">HP:0100747<a name=\"hpo-HP.580100747\"> </a></td><td>Macrodactyly of toe</td></tr><tr><td style=\"white-space:nowrap\">HP:0002109<a name=\"hpo-HP.580002109\"> </a></td><td>obsolete Abnormality of the bronchi</td></tr><tr><td style=\"white-space:nowrap\">HP:0011950<a name=\"hpo-HP.580011950\"> </a></td><td>Bronchiolitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002850<a name=\"hpo-HP.580002850\"> </a></td><td>Decreased circulating total IgM</td></tr><tr><td style=\"white-space:nowrap\">HP:0001395<a name=\"hpo-HP.580001395\"> </a></td><td>Hepatic fibrosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0010701<a name=\"hpo-HP.580010701\"> </a></td><td>Abnormal immunoglobulin level</td></tr><tr><td style=\"white-space:nowrap\">HP:0009928<a name=\"hpo-HP.580009928\"> </a></td><td>Thick nasal alae</td></tr><tr><td style=\"white-space:nowrap\">HP:0010807<a name=\"hpo-HP.580010807\"> </a></td><td>Open bite</td></tr><tr><td style=\"white-space:nowrap\">HP:0002126<a name=\"hpo-HP.580002126\"> </a></td><td>Polymicrogyria</td></tr><tr><td style=\"white-space:nowrap\">HP:0002900<a name=\"hpo-HP.580002900\"> </a></td><td>Hypokalemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000155<a name=\"hpo-HP.580000155\"> </a></td><td>Oral ulcer</td></tr><tr><td style=\"white-space:nowrap\">HP:0000135<a name=\"hpo-HP.580000135\"> </a></td><td>Hypogonadism</td></tr><tr><td style=\"white-space:nowrap\">HP:0100783<a name=\"hpo-HP.580100783\"> </a></td><td>Breast aplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000336<a name=\"hpo-HP.580000336\"> </a></td><td>Prominent supraorbital ridges</td></tr><tr><td style=\"white-space:nowrap\">HP:0010557<a name=\"hpo-HP.580010557\"> </a></td><td>Overlapping fingers</td></tr><tr><td style=\"white-space:nowrap\">HP:0005100<a name=\"hpo-HP.580005100\"> </a></td><td>Premature birth following premature rupture of fetal membranes</td></tr><tr><td style=\"white-space:nowrap\">HP:0002594<a name=\"hpo-HP.580002594\"> </a></td><td>Pancreatic hypoplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0010109<a name=\"hpo-HP.580010109\"> </a></td><td>Short hallux</td></tr><tr><td style=\"white-space:nowrap\">HP:0002334<a name=\"hpo-HP.580002334\"> </a></td><td>Abnormality of the cerebellar vermis</td></tr><tr><td style=\"white-space:nowrap\">HP:0003326<a name=\"hpo-HP.580003326\"> </a></td><td>Myalgia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001645<a name=\"hpo-HP.580001645\"> </a></td><td>Sudden cardiac death</td></tr><tr><td style=\"white-space:nowrap\">HP:0001612<a name=\"hpo-HP.580001612\"> </a></td><td>Weak cry</td></tr><tr><td style=\"white-space:nowrap\">HP:0001618<a name=\"hpo-HP.580001618\"> </a></td><td>Dysphonia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001336<a name=\"hpo-HP.580001336\"> </a></td><td>Myoclonus</td></tr><tr><td style=\"white-space:nowrap\">HP:0001283<a name=\"hpo-HP.580001283\"> </a></td><td>Bulbar palsy</td></tr><tr><td style=\"white-space:nowrap\">HP:0002080<a name=\"hpo-HP.580002080\"> </a></td><td>Intention tremor</td></tr><tr><td style=\"white-space:nowrap\">HP:0002174<a name=\"hpo-HP.580002174\"> </a></td><td>Postural tremor</td></tr><tr><td style=\"white-space:nowrap\">HP:0002064<a name=\"hpo-HP.580002064\"> </a></td><td>Spastic gait</td></tr><tr><td style=\"white-space:nowrap\">HP:0009800<a name=\"hpo-HP.580009800\"> </a></td><td>Maternal diabetes</td></tr><tr><td style=\"white-space:nowrap\">HP:0001662<a name=\"hpo-HP.580001662\"> </a></td><td>Bradycardia</td></tr><tr><td style=\"white-space:nowrap\">HP:0006595<a name=\"hpo-HP.580006595\"> </a></td><td>Scapulohumeral synostosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0005815<a name=\"hpo-HP.580005815\"> </a></td><td>Supernumerary ribs</td></tr><tr><td style=\"white-space:nowrap\">HP:0000307<a name=\"hpo-HP.580000307\"> </a></td><td>Pointed chin</td></tr><tr><td style=\"white-space:nowrap\">HP:0012371<a name=\"hpo-HP.580012371\"> </a></td><td>Hyperplasia of midface</td></tr><tr><td style=\"white-space:nowrap\">HP:0002643<a name=\"hpo-HP.580002643\"> </a></td><td>Neonatal respiratory distress</td></tr><tr><td style=\"white-space:nowrap\">HP:0002093<a name=\"hpo-HP.580002093\"> </a></td><td>Respiratory insufficiency</td></tr><tr><td style=\"white-space:nowrap\">HP:0010310<a name=\"hpo-HP.580010310\"> </a></td><td>Chylothorax</td></tr><tr><td style=\"white-space:nowrap\">HP:0006376<a name=\"hpo-HP.580006376\"> </a></td><td>Limited elbow flexion</td></tr><tr><td style=\"white-space:nowrap\">HP:0006467<a name=\"hpo-HP.580006467\"> </a></td><td>Limited shoulder movement</td></tr><tr><td style=\"white-space:nowrap\">HP:0010505<a name=\"hpo-HP.580010505\"> </a></td><td>Limitation of movement at ankles</td></tr><tr><td style=\"white-space:nowrap\">HP:0010501<a name=\"hpo-HP.580010501\"> </a></td><td>Limitation of knee mobility</td></tr><tr><td style=\"white-space:nowrap\">HP:0009896<a name=\"hpo-HP.580009896\"> </a></td><td>Abnormality of the antitragus</td></tr><tr><td style=\"white-space:nowrap\">HP:0004404<a name=\"hpo-HP.580004404\"> </a></td><td>Abnormal nipple morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0011957<a name=\"hpo-HP.580011957\"> </a></td><td>Abnormal pectoral muscle morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0000777<a name=\"hpo-HP.580000777\"> </a></td><td>Abnormality of the thymus</td></tr><tr><td style=\"white-space:nowrap\">HP:0000418<a name=\"hpo-HP.580000418\"> </a></td><td>Narrow nasal ridge</td></tr><tr><td style=\"white-space:nowrap\">HP:0001572<a name=\"hpo-HP.580001572\"> </a></td><td>Macrodontia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002967<a name=\"hpo-HP.580002967\"> </a></td><td>Cubitus valgus</td></tr><tr><td style=\"white-space:nowrap\">HP:0000988<a name=\"hpo-HP.580000988\"> </a></td><td>Skin rash</td></tr><tr><td style=\"white-space:nowrap\">HP:0009733<a name=\"hpo-HP.580009733\"> </a></td><td>Glioma</td></tr><tr><td style=\"white-space:nowrap\">HP:0012452<a name=\"hpo-HP.580012452\"> </a></td><td>Restless legs</td></tr><tr><td style=\"white-space:nowrap\">HP:0100031<a name=\"hpo-HP.580100031\"> </a></td><td>Neoplasm of the thyroid gland</td></tr><tr><td style=\"white-space:nowrap\">HP:0030127<a name=\"hpo-HP.580030127\"> </a></td><td>Endometriosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0000123<a name=\"hpo-HP.580000123\"> </a></td><td>Nephritis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001974<a name=\"hpo-HP.580001974\"> </a></td><td>Leukocytosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0010976<a name=\"hpo-HP.580010976\"> </a></td><td>B lymphocytopenia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000010<a name=\"hpo-HP.580000010\"> </a></td><td>Recurrent urinary tract infections</td></tr><tr><td style=\"white-space:nowrap\">HP:0100807<a name=\"hpo-HP.580100807\"> </a></td><td>Long fingers</td></tr><tr><td style=\"white-space:nowrap\">HP:0000653<a name=\"hpo-HP.580000653\"> </a></td><td>Sparse eyelashes</td></tr><tr><td style=\"white-space:nowrap\">HP:0000171<a name=\"hpo-HP.580000171\"> </a></td><td>Microglossia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002575<a name=\"hpo-HP.580002575\"> </a></td><td>Tracheoesophageal fistula</td></tr><tr><td style=\"white-space:nowrap\">HP:0009933<a name=\"hpo-HP.580009933\"> </a></td><td>Narrow naris</td></tr><tr><td style=\"white-space:nowrap\">HP:0000883<a name=\"hpo-HP.580000883\"> </a></td><td>Thin ribs</td></tr><tr><td style=\"white-space:nowrap\">HP:0000121<a name=\"hpo-HP.580000121\"> </a></td><td>Nephrocalcinosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001349<a name=\"hpo-HP.580001349\"> </a></td><td>Facial diplegia</td></tr><tr><td style=\"white-space:nowrap\">HP:0012037<a name=\"hpo-HP.580012037\"> </a></td><td>Pectoralis amyotrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0100560<a name=\"hpo-HP.580100560\"> </a></td><td>Upper limb asymmetry</td></tr><tr><td style=\"white-space:nowrap\">HP:0005684<a name=\"hpo-HP.580005684\"> </a></td><td>Distal arthrogryposis</td></tr><tr><td style=\"white-space:nowrap\">HP:0010722<a name=\"hpo-HP.580010722\"> </a></td><td>Asymmetry of the ears</td></tr><tr><td style=\"white-space:nowrap\">HP:0009380<a name=\"hpo-HP.580009380\"> </a></td><td>Aplasia of the fingers</td></tr><tr><td style=\"white-space:nowrap\">HP:0001657<a name=\"hpo-HP.580001657\"> </a></td><td>Prolonged QT interval</td></tr><tr><td style=\"white-space:nowrap\">HP:0002040<a name=\"hpo-HP.580002040\"> </a></td><td>Esophageal varix</td></tr><tr><td style=\"white-space:nowrap\">HP:0000613<a name=\"hpo-HP.580000613\"> </a></td><td>Photophobia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000561<a name=\"hpo-HP.580000561\"> </a></td><td>Absent eyelashes</td></tr><tr><td style=\"white-space:nowrap\">HP:0002223<a name=\"hpo-HP.580002223\"> </a></td><td>Absent eyebrow</td></tr><tr><td style=\"white-space:nowrap\">HP:0002591<a name=\"hpo-HP.580002591\"> </a></td><td>Polyphagia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002373<a name=\"hpo-HP.580002373\"> </a></td><td>Febrile seizure (within the age range of 3 months to 6 years)</td></tr><tr><td style=\"white-space:nowrap\">HP:0002419<a name=\"hpo-HP.580002419\"> </a></td><td>Molar tooth sign on MRI</td></tr><tr><td style=\"white-space:nowrap\">HP:0001010<a name=\"hpo-HP.580001010\"> </a></td><td>Hypopigmentation of the skin</td></tr><tr><td style=\"white-space:nowrap\">HP:0005772<a name=\"hpo-HP.580005772\"> </a></td><td>Aplasia/Hypoplasia of the tibia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002211<a name=\"hpo-HP.580002211\"> </a></td><td>White forelock</td></tr><tr><td style=\"white-space:nowrap\">HP:0007126<a name=\"hpo-HP.580007126\"> </a></td><td>Proximal amyotrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0003798<a name=\"hpo-HP.580003798\"> </a></td><td>Nemaline bodies</td></tr><tr><td style=\"white-space:nowrap\">HP:0006533<a name=\"hpo-HP.580006533\"> </a></td><td>Bronchodysplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0003391<a name=\"hpo-HP.580003391\"> </a></td><td>Gowers sign</td></tr><tr><td style=\"white-space:nowrap\">HP:0000771<a name=\"hpo-HP.580000771\"> </a></td><td>Gynecomastia</td></tr><tr><td style=\"white-space:nowrap\">HP:0100785<a name=\"hpo-HP.580100785\"> </a></td><td>Insomnia</td></tr><tr><td style=\"white-space:nowrap\">HP:0010529<a name=\"hpo-HP.580010529\"> </a></td><td>Echolalia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000363<a name=\"hpo-HP.580000363\"> </a></td><td>Abnormality of earlobe</td></tr><tr><td style=\"white-space:nowrap\">HP:0002612<a name=\"hpo-HP.580002612\"> </a></td><td>Congenital hepatic fibrosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0006721<a name=\"hpo-HP.580006721\"> </a></td><td>Acute lymphoblastic leukemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001958<a name=\"hpo-HP.580001958\"> </a></td><td>Nonketotic hypoglycemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0003457<a name=\"hpo-HP.580003457\"> </a></td><td>EMG abnormality</td></tr><tr><td style=\"white-space:nowrap\">HP:0010636<a name=\"hpo-HP.580010636\"> </a></td><td>Schizencephaly</td></tr><tr><td style=\"white-space:nowrap\">HP:0005266<a name=\"hpo-HP.580005266\"> </a></td><td>Intestinal polyp</td></tr><tr><td style=\"white-space:nowrap\">HP:0200063<a name=\"hpo-HP.580200063\"> </a></td><td>Colorectal polyposis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001762<a name=\"hpo-HP.580001762\"> </a></td><td>Talipes equinovarus</td></tr><tr><td style=\"white-space:nowrap\">HP:0000056<a name=\"hpo-HP.580000056\"> </a></td><td>Abnormality of the clitoris</td></tr><tr><td style=\"white-space:nowrap\">HP:0008655<a name=\"hpo-HP.580008655\"> </a></td><td>Aplasia/Hypoplasia of the fallopian tube</td></tr><tr><td style=\"white-space:nowrap\">HP:0002072<a name=\"hpo-HP.580002072\"> </a></td><td>Chorea</td></tr><tr><td style=\"white-space:nowrap\">HP:0008734<a name=\"hpo-HP.580008734\"> </a></td><td>Decreased testicular size</td></tr><tr><td style=\"white-space:nowrap\">HP:0002136<a name=\"hpo-HP.580002136\"> </a></td><td>Broad-based gait</td></tr><tr><td style=\"white-space:nowrap\">HP:0010958<a name=\"hpo-HP.580010958\"> </a></td><td>Bilateral renal agenesis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002510<a name=\"hpo-HP.580002510\"> </a></td><td>Spastic tetraplegia</td></tr><tr><td style=\"white-space:nowrap\">HP:0003234<a name=\"hpo-HP.580003234\"> </a></td><td>Decreased plasma carnitine</td></tr><tr><td style=\"white-space:nowrap\">HP:0000720<a name=\"hpo-HP.580000720\"> </a></td><td>Mood swings</td></tr><tr><td style=\"white-space:nowrap\">HP:0012638<a name=\"hpo-HP.580012638\"> </a></td><td>Abnormal nervous system physiology</td></tr><tr><td style=\"white-space:nowrap\">HP:0002803<a name=\"hpo-HP.580002803\"> </a></td><td>Congenital contracture</td></tr><tr><td style=\"white-space:nowrap\">HP:0000152<a name=\"hpo-HP.580000152\"> </a></td><td>Abnormality of head or neck</td></tr><tr><td style=\"white-space:nowrap\">HP:0004377<a name=\"hpo-HP.580004377\"> </a></td><td>Hematological neoplasm</td></tr><tr><td style=\"white-space:nowrap\">HP:0100006<a name=\"hpo-HP.580100006\"> </a></td><td>Neoplasm of the central nervous system</td></tr><tr><td style=\"white-space:nowrap\">HP:0012759<a name=\"hpo-HP.580012759\"> </a></td><td>Neurodevelopmental abnormality</td></tr><tr><td style=\"white-space:nowrap\">HP:0011805<a name=\"hpo-HP.580011805\"> </a></td><td>Abnormal skeletal muscle morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0003634<a name=\"hpo-HP.580003634\"> </a></td><td>Amyoplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001507<a name=\"hpo-HP.580001507\"> </a></td><td>Growth abnormality</td></tr><tr><td style=\"white-space:nowrap\">HP:0001939<a name=\"hpo-HP.580001939\"> </a></td><td>Abnormality of metabolism/homeostasis</td></tr><tr><td style=\"white-space:nowrap\">HP:0011013<a name=\"hpo-HP.580011013\"> </a></td><td>Abnormal circulating carbohydrate concentration</td></tr><tr><td style=\"white-space:nowrap\">HP:0410008<a name=\"hpo-HP.580410008\"> </a></td><td>Abnormality of the peripheral nervous system</td></tr><tr><td style=\"white-space:nowrap\">HP:0200134<a name=\"hpo-HP.580200134\"> </a></td><td>Epileptic encephalopathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0001881<a name=\"hpo-HP.580001881\"> </a></td><td>Abnormal leukocyte morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0005549<a name=\"hpo-HP.580005549\"> </a></td><td>obsolete Congenital neutropenia</td></tr><tr><td style=\"white-space:nowrap\">HP:0004439<a name=\"hpo-HP.580004439\"> </a></td><td>Craniofacial dysostosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0012443<a name=\"hpo-HP.580012443\"> </a></td><td>Abnormality of brain morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0000202<a name=\"hpo-HP.580000202\"> </a></td><td>Oral cleft</td></tr><tr><td style=\"white-space:nowrap\">HP:0011842<a name=\"hpo-HP.580011842\"> </a></td><td>Abnormality of skeletal morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0003808<a name=\"hpo-HP.580003808\"> </a></td><td>Abnormal muscle tone</td></tr><tr><td style=\"white-space:nowrap\">HP:0001574<a name=\"hpo-HP.580001574\"> </a></td><td>Abnormality of the integument</td></tr><tr><td style=\"white-space:nowrap\">HP:0030056<a name=\"hpo-HP.580030056\"> </a></td><td>Uncombable hair</td></tr><tr><td style=\"white-space:nowrap\">HP:0003549<a name=\"hpo-HP.580003549\"> </a></td><td>Abnormality of connective tissue</td></tr><tr><td style=\"white-space:nowrap\">HP:0030875<a name=\"hpo-HP.580030875\"> </a></td><td>Abnormality of pulmonary circulation</td></tr><tr><td style=\"white-space:nowrap\">HP:0000118<a name=\"hpo-HP.580000118\"> </a></td><td>Phenotypic abnormality</td></tr><tr><td style=\"white-space:nowrap\">HP:0012469<a name=\"hpo-HP.580012469\"> </a></td><td>Infantile spasms</td></tr><tr><td style=\"white-space:nowrap\">HP:0032894<a name=\"hpo-HP.580032894\"> </a></td><td>Seizure precipitated by febrile infection</td></tr><tr><td style=\"white-space:nowrap\">HP:0100661<a name=\"hpo-HP.580100661\"> </a></td><td>Trigeminal neuralgia</td></tr><tr><td style=\"white-space:nowrap\">HP:0012207<a name=\"hpo-HP.580012207\"> </a></td><td>Reduced sperm motility</td></tr><tr><td style=\"white-space:nowrap\">HP:0000798<a name=\"hpo-HP.580000798\"> </a></td><td>Oligospermia</td></tr><tr><td style=\"white-space:nowrap\">HP:0012864<a name=\"hpo-HP.580012864\"> </a></td><td>Abnormal sperm morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0008232<a name=\"hpo-HP.580008232\"> </a></td><td>Elevated circulating follicle stimulating hormone level</td></tr><tr><td style=\"white-space:nowrap\">HP:0040306<a name=\"hpo-HP.580040306\"> </a></td><td>Decreased male libido</td></tr><tr><td style=\"white-space:nowrap\">HP:0012208<a name=\"hpo-HP.580012208\"> </a></td><td>Immotile sperm</td></tr><tr><td style=\"white-space:nowrap\">HP:0000027<a name=\"hpo-HP.580000027\"> </a></td><td>Azoospermia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000870<a name=\"hpo-HP.580000870\"> </a></td><td>Increased circulating prolactin concentration</td></tr><tr><td style=\"white-space:nowrap\">HP:0008187<a name=\"hpo-HP.580008187\"> </a></td><td>Absence of secondary sex characteristics</td></tr><tr><td style=\"white-space:nowrap\">HP:0010469<a name=\"hpo-HP.580010469\"> </a></td><td>Absent testis</td></tr><tr><td style=\"white-space:nowrap\">HP:0011969<a name=\"hpo-HP.580011969\"> </a></td><td>Elevated circulating luteinizing hormone level</td></tr><tr><td style=\"white-space:nowrap\">HP:0040171<a name=\"hpo-HP.580040171\"> </a></td><td>Decreased serum testosterone level</td></tr><tr><td style=\"white-space:nowrap\">HP:0003251<a name=\"hpo-HP.580003251\"> </a></td><td>Male infertility</td></tr><tr><td style=\"white-space:nowrap\">HP:0009804<a name=\"hpo-HP.580009804\"> </a></td><td>Reduced number of teeth</td></tr><tr><td style=\"white-space:nowrap\">HP:0000548<a name=\"hpo-HP.580000548\"> </a></td><td>Cone/cone-rod dystrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0000546<a name=\"hpo-HP.580000546\"> </a></td><td>Retinal degeneration</td></tr><tr><td style=\"white-space:nowrap\">HP:0008002<a name=\"hpo-HP.580008002\"> </a></td><td>Abnormality of macular pigmentation</td></tr><tr><td style=\"white-space:nowrap\">HP:0000608<a name=\"hpo-HP.580000608\"> </a></td><td>Macular degeneration</td></tr><tr><td style=\"white-space:nowrap\">HP:0030611<a name=\"hpo-HP.580030611\"> </a></td><td>Retinal pigment epithelial loss on macular OCT</td></tr><tr><td style=\"white-space:nowrap\">HP:0001135<a name=\"hpo-HP.580001135\"> </a></td><td>Chorioretinal dystrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0030468<a name=\"hpo-HP.580030468\"> </a></td><td>Abnormal multifocal electroretinogram</td></tr><tr><td style=\"white-space:nowrap\">HP:00030532<a name=\"hpo-HP.5800030532\"> </a></td><td>Visual acuity test abnormality</td></tr><tr><td style=\"white-space:nowrap\">HP:0007401<a name=\"hpo-HP.580007401\"> </a></td><td>Macular atrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0030466<a name=\"hpo-HP.580030466\"> </a></td><td>Abnormal full-field electroretinogram</td></tr><tr><td style=\"white-space:nowrap\">HP:007737<a name=\"hpo-HP.58007737\"> </a></td><td>Bone spicule pigmentation of the retina</td></tr><tr><td style=\"white-space:nowrap\">HP:0011342<a name=\"hpo-HP.580011342\"> </a></td><td>Mild global developmental delay</td></tr><tr><td style=\"white-space:nowrap\">HP:0030610<a name=\"hpo-HP.580030610\"> </a></td><td>Photoreceptor outer segment loss on macular OCT</td></tr><tr><td style=\"white-space:nowrap\">HP:0007722<a name=\"hpo-HP.580007722\"> </a></td><td>Retinal pigment epithelial atrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0030493<a name=\"hpo-HP.580030493\"> </a></td><td>Abnormality of foveal pigmentation</td></tr><tr><td style=\"white-space:nowrap\">HP:0007843<a name=\"hpo-HP.580007843\"> </a></td><td>Attenuation of retinal blood vessels</td></tr><tr><td style=\"white-space:nowrap\">HP:0007754<a name=\"hpo-HP.580007754\"> </a></td><td>Macular dystrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0011509<a name=\"hpo-HP.580011509\"> </a></td><td>Macular hyperpigmentation</td></tr><tr><td style=\"white-space:nowrap\">HP:0008527<a name=\"hpo-HP.580008527\"> </a></td><td>Congenital sensorineural hearing impairment</td></tr><tr><td style=\"white-space:nowrap\">HP:0200070<a name=\"hpo-HP.580200070\"> </a></td><td>Peripheral retinal atrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0007793<a name=\"hpo-HP.580007793\"> </a></td><td>Granular macular appearance</td></tr><tr><td style=\"white-space:nowrap\">HP:0007987<a name=\"hpo-HP.580007987\"> </a></td><td>Progressive visual field defects</td></tr><tr><td style=\"white-space:nowrap\">HP:0100817<a name=\"hpo-HP.580100817\"> </a></td><td>Renovascular hypertension</td></tr><tr><td style=\"white-space:nowrap\">HP:0007868<a name=\"hpo-HP.580007868\"> </a></td><td>obsolete Age-related macular degeneration</td></tr><tr><td style=\"white-space:nowrap\">HP:0030527<a name=\"hpo-HP.580030527\"> </a></td><td>Very severe constriction of peripheral visual field</td></tr><tr><td style=\"white-space:nowrap\">HP:0030551<a name=\"hpo-HP.580030551\"> </a></td><td>Visual acuity light perception with projection</td></tr><tr><td style=\"white-space:nowrap\">HP:0011505<a name=\"hpo-HP.580011505\"> </a></td><td>Cystoid macular edema</td></tr><tr><td style=\"white-space:nowrap\">HP:0010442<a name=\"hpo-HP.580010442\"> </a></td><td>Polydactyly</td></tr><tr><td style=\"white-space:nowrap\">HP:0007642<a name=\"hpo-HP.580007642\"> </a></td><td>Congenital stationary night blindness</td></tr><tr><td style=\"white-space:nowrap\">HP:0009073<a name=\"hpo-HP.580009073\"> </a></td><td>Progressive proximal muscle weakness</td></tr><tr><td style=\"white-space:nowrap\">HP:0003741<a name=\"hpo-HP.580003741\"> </a></td><td>Congenital muscular dystrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0100299<a name=\"hpo-HP.580100299\"> </a></td><td>Muscle fiber inclusion bodies</td></tr><tr><td style=\"white-space:nowrap\">HP:0003540<a name=\"hpo-HP.580003540\"> </a></td><td>Impaired platelet aggregation</td></tr><tr><td style=\"white-space:nowrap\">HP:0010489<a name=\"hpo-HP.580010489\"> </a></td><td>Absent palmar crease</td></tr><tr><td style=\"white-space:nowrap\">HP:0009824<a name=\"hpo-HP.580009824\"> </a></td><td>Upper limb undergrowth</td></tr><tr><td style=\"white-space:nowrap\">HP:0002395<a name=\"hpo-HP.580002395\"> </a></td><td>Lower limb hyperreflexia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001138<a name=\"hpo-HP.580001138\"> </a></td><td>Optic neuropathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0007103<a name=\"hpo-HP.580007103\"> </a></td><td>Hypointensity of cerebral white matter on MRI</td></tr><tr><td style=\"white-space:nowrap\">HP:0003458<a name=\"hpo-HP.580003458\"> </a></td><td>EMG: myopathic abnormalities</td></tr><tr><td style=\"white-space:nowrap\">HP:0002987<a name=\"hpo-HP.580002987\"> </a></td><td>Elbow flexion contracture</td></tr><tr><td style=\"white-space:nowrap\">HP:0006466<a name=\"hpo-HP.580006466\"> </a></td><td>Ankle flexion contracture</td></tr><tr><td style=\"white-space:nowrap\">HP:0008458<a name=\"hpo-HP.580008458\"> </a></td><td>Progressive congenital scoliosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0000473<a name=\"hpo-HP.580000473\"> </a></td><td>Torticollis</td></tr><tr><td style=\"white-space:nowrap\">HP:0011800<a name=\"hpo-HP.580011800\"> </a></td><td>Midface retrusion</td></tr><tr><td style=\"white-space:nowrap\">HP:0000597<a name=\"hpo-HP.580000597\"> </a></td><td>Ophthalmoparesis</td></tr><tr><td style=\"white-space:nowrap\">HP:0005853<a name=\"hpo-HP.580005853\"> </a></td><td>Congenital foot contraction deformities</td></tr><tr><td style=\"white-space:nowrap\">HP:0007002<a name=\"hpo-HP.580007002\"> </a></td><td>Motor axonal neuropathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0003327<a name=\"hpo-HP.580003327\"> </a></td><td>Axial muscle weakness</td></tr><tr><td style=\"white-space:nowrap\">HP:0003306<a name=\"hpo-HP.580003306\"> </a></td><td>Spinal rigidity</td></tr><tr><td style=\"white-space:nowrap\">HP:0002068<a name=\"hpo-HP.580002068\"> </a></td><td>Neuromuscular dysphagia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001002<a name=\"hpo-HP.580001002\"> </a></td><td>obsolete Decreased subcutaneous fat</td></tr><tr><td style=\"white-space:nowrap\">HP:0002880<a name=\"hpo-HP.580002880\"> </a></td><td>obsolete Respiratory difficulties</td></tr><tr><td style=\"white-space:nowrap\">HP:0006829<a name=\"hpo-HP.580006829\"> </a></td><td>Severe muscular hypotonia</td></tr><tr><td style=\"white-space:nowrap\">HP:0011448<a name=\"hpo-HP.580011448\"> </a></td><td>Ankle clonus</td></tr><tr><td style=\"white-space:nowrap\">HP:0003487<a name=\"hpo-HP.580003487\"> </a></td><td>Babinski sign</td></tr><tr><td style=\"white-space:nowrap\">HP:0002378<a name=\"hpo-HP.580002378\"> </a></td><td>Hand tremor</td></tr><tr><td style=\"white-space:nowrap\">HP:0002747<a name=\"hpo-HP.580002747\"> </a></td><td>Respiratory insufficiency due to muscle weakness</td></tr><tr><td style=\"white-space:nowrap\">HP:0002579<a name=\"hpo-HP.580002579\"> </a></td><td>Gastrointestinal dysmotility</td></tr><tr><td style=\"white-space:nowrap\">HP:0001041<a name=\"hpo-HP.580001041\"> </a></td><td>Facial erythema</td></tr><tr><td style=\"white-space:nowrap\">HP:0040180<a name=\"hpo-HP.580040180\"> </a></td><td>Hyperkeratosis pilaris</td></tr><tr><td style=\"white-space:nowrap\">HP:0001382<a name=\"hpo-HP.580001382\"> </a></td><td>Joint hypermobility</td></tr><tr><td style=\"white-space:nowrap\">HP:0003722<a name=\"hpo-HP.580003722\"> </a></td><td>Neck flexor weakness</td></tr><tr><td style=\"white-space:nowrap\">HP:0003323<a name=\"hpo-HP.580003323\"> </a></td><td>Progressive muscle weakness</td></tr><tr><td style=\"white-space:nowrap\">HP:0002380<a name=\"hpo-HP.580002380\"> </a></td><td>Fasciculations</td></tr><tr><td style=\"white-space:nowrap\">HP:0012785<a name=\"hpo-HP.580012785\"> </a></td><td>Flexion contracture of finger</td></tr><tr><td style=\"white-space:nowrap\">HP:0007936<a name=\"hpo-HP.580007936\"> </a></td><td>Restrictive external ophthalmoplegia</td></tr><tr><td style=\"white-space:nowrap\">HP:0030319<a name=\"hpo-HP.580030319\"> </a></td><td>Weakness of facial musculature</td></tr><tr><td style=\"white-space:nowrap\">HP:0008936<a name=\"hpo-HP.580008936\"> </a></td><td>Muscular hypotonia of the trunk</td></tr><tr><td style=\"white-space:nowrap\">HP:0030230<a name=\"hpo-HP.580030230\"> </a></td><td>Central core regions in muscle fibers</td></tr><tr><td style=\"white-space:nowrap\">HP:0011471<a name=\"hpo-HP.580011471\"> </a></td><td>Gastrostomy tube feeding in infancy</td></tr><tr><td style=\"white-space:nowrap\">HP:0001290<a name=\"hpo-HP.580001290\"> </a></td><td>Generalized hypotonia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002421<a name=\"hpo-HP.580002421\"> </a></td><td>Poor head control</td></tr><tr><td style=\"white-space:nowrap\">HP:0010301<a name=\"hpo-HP.580010301\"> </a></td><td>Spinal dysraphism</td></tr><tr><td style=\"white-space:nowrap\">HP:0004303<a name=\"hpo-HP.580004303\"> </a></td><td>Abnormal muscle fiber morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0009046<a name=\"hpo-HP.580009046\"> </a></td><td>Difficulty running</td></tr><tr><td style=\"white-space:nowrap\">HP:0003715<a name=\"hpo-HP.580003715\"> </a></td><td>Myofibrillar myopathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0000467<a name=\"hpo-HP.580000467\"> </a></td><td>Neck muscle weakness</td></tr><tr><td style=\"white-space:nowrap\">HP:0001999<a name=\"hpo-HP.580001999\"> </a></td><td>Abnormal facial shape</td></tr><tr><td style=\"white-space:nowrap\">HP:0002751<a name=\"hpo-HP.580002751\"> </a></td><td>Kyphoscoliosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0030223<a name=\"hpo-HP.580030223\"> </a></td><td>Perseveration</td></tr><tr><td style=\"white-space:nowrap\">HP:0002344<a name=\"hpo-HP.580002344\"> </a></td><td>Progressive neurologic deterioration</td></tr><tr><td style=\"white-space:nowrap\">HP:0002522<a name=\"hpo-HP.580002522\"> </a></td><td>Areflexia of lower limbs</td></tr><tr><td style=\"white-space:nowrap\">HP:0003805<a name=\"hpo-HP.580003805\"> </a></td><td>Rimmed vacuoles</td></tr><tr><td style=\"white-space:nowrap\">HP:0005781<a name=\"hpo-HP.580005781\"> </a></td><td>Contractures of the large joints</td></tr><tr><td style=\"white-space:nowrap\">HP:0040083<a name=\"hpo-HP.580040083\"> </a></td><td>Toe walking</td></tr><tr><td style=\"white-space:nowrap\">HP:0003749<a name=\"hpo-HP.580003749\"> </a></td><td>Pelvic girdle muscle weakness</td></tr><tr><td style=\"white-space:nowrap\">HP:0012444<a name=\"hpo-HP.580012444\"> </a></td><td>Brain atrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0003738<a name=\"hpo-HP.580003738\"> </a></td><td>Exercise-induced myalgia</td></tr><tr><td style=\"white-space:nowrap\">HP:0003756<a name=\"hpo-HP.580003756\"> </a></td><td>Skeletal myopathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0002492<a name=\"hpo-HP.580002492\"> </a></td><td>Morphological abnormality of the corticospinal tract</td></tr><tr><td style=\"white-space:nowrap\">HP:0100302<a name=\"hpo-HP.580100302\"> </a></td><td>Muscle fiber tubuloreticular inclusions</td></tr><tr><td style=\"white-space:nowrap\">HP:0006817<a name=\"hpo-HP.580006817\"> </a></td><td>Aplasia/Hypoplasia of the cerebellar vermis</td></tr><tr><td style=\"white-space:nowrap\">HP:0003473<a name=\"hpo-HP.580003473\"> </a></td><td>Fatigable weakness</td></tr><tr><td style=\"white-space:nowrap\">HP:0002077<a name=\"hpo-HP.580002077\"> </a></td><td>Migraine with aura</td></tr><tr><td style=\"white-space:nowrap\">HP:0100559<a name=\"hpo-HP.580100559\"> </a></td><td>Lower limb asymmetry</td></tr><tr><td style=\"white-space:nowrap\">HP:0002079<a name=\"hpo-HP.580002079\"> </a></td><td>Hypoplasia of the corpus callosum</td></tr><tr><td style=\"white-space:nowrap\">HP:0002804<a name=\"hpo-HP.580002804\"> </a></td><td>Arthrogryposis multiplex congenita</td></tr><tr><td style=\"white-space:nowrap\">HP:0011623<a name=\"hpo-HP.580011623\"> </a></td><td>Muscular ventricular septal defect</td></tr><tr><td style=\"white-space:nowrap\">HP:0002191<a name=\"hpo-HP.580002191\"> </a></td><td>Progressive spasticity</td></tr><tr><td style=\"white-space:nowrap\">HP:0003390<a name=\"hpo-HP.580003390\"> </a></td><td>Sensory axonal neuropathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0006986<a name=\"hpo-HP.580006986\"> </a></td><td>Upper limb spasticity</td></tr><tr><td style=\"white-space:nowrap\">HP:0002464<a name=\"hpo-HP.580002464\"> </a></td><td>Spastic dysarthria</td></tr><tr><td style=\"white-space:nowrap\">HP:0001308<a name=\"hpo-HP.580001308\"> </a></td><td>Tongue fasciculations</td></tr><tr><td style=\"white-space:nowrap\">HP:0007010<a name=\"hpo-HP.580007010\"> </a></td><td>Poor fine motor coordination</td></tr><tr><td style=\"white-space:nowrap\">HP:0003737<a name=\"hpo-HP.580003737\"> </a></td><td>Mitochondrial myopathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0008012<a name=\"hpo-HP.580008012\"> </a></td><td>obsolete Congenital myopia</td></tr><tr><td style=\"white-space:nowrap\">HP:0008872<a name=\"hpo-HP.580008872\"> </a></td><td>Feeding difficulties in infancy</td></tr><tr><td style=\"white-space:nowrap\">HP:0005750<a name=\"hpo-HP.580005750\"> </a></td><td>Contractures of the joints of the lower limbs</td></tr><tr><td style=\"white-space:nowrap\">HP:0009067<a name=\"hpo-HP.580009067\"> </a></td><td>Progressive spinal muscular atrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0001623<a name=\"hpo-HP.580001623\"> </a></td><td>Breech presentation</td></tr><tr><td style=\"white-space:nowrap\">HP:0001374<a name=\"hpo-HP.580001374\"> </a></td><td>Congenital hip dislocation</td></tr><tr><td style=\"white-space:nowrap\">HP:0002359<a name=\"hpo-HP.580002359\"> </a></td><td>Frequent falls</td></tr><tr><td style=\"white-space:nowrap\">HP:0003803<a name=\"hpo-HP.580003803\"> </a></td><td>Type 1 muscle fiber predominance</td></tr><tr><td style=\"white-space:nowrap\">HP:0011410<a name=\"hpo-HP.580011410\"> </a></td><td>Caesarian section</td></tr><tr><td style=\"white-space:nowrap\">HP:0008947<a name=\"hpo-HP.580008947\"> </a></td><td>Infantile muscular hypotonia</td></tr><tr><td style=\"white-space:nowrap\">HP:0100501<a name=\"hpo-HP.580100501\"> </a></td><td>Recurrent bronchiolitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0003789<a name=\"hpo-HP.580003789\"> </a></td><td>Minicore myopathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0000544<a name=\"hpo-HP.580000544\"> </a></td><td>External ophthalmoplegia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001605<a name=\"hpo-HP.580001605\"> </a></td><td>Vocal cord paralysis</td></tr><tr><td style=\"white-space:nowrap\">HP:0003712<a name=\"hpo-HP.580003712\"> </a></td><td>Skeletal muscle hypertrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0012507<a name=\"hpo-HP.580012507\"> </a></td><td>Weakness of orbicularis oculi muscle</td></tr><tr><td style=\"white-space:nowrap\">HP:0009816<a name=\"hpo-HP.580009816\"> </a></td><td>Lower limb undergrowth</td></tr><tr><td style=\"white-space:nowrap\">HP:0008935<a name=\"hpo-HP.580008935\"> </a></td><td>Generalized neonatal hypotonia</td></tr><tr><td style=\"white-space:nowrap\">HP:0003484<a name=\"hpo-HP.580003484\"> </a></td><td>Upper limb muscle weakness</td></tr><tr><td style=\"white-space:nowrap\">HP:0008331<a name=\"hpo-HP.580008331\"> </a></td><td>Elevated creatine kinase after exercise</td></tr><tr><td style=\"white-space:nowrap\">HP:0001315<a name=\"hpo-HP.580001315\"> </a></td><td>Reduced tendon reflexes</td></tr><tr><td style=\"white-space:nowrap\">HP:0012473<a name=\"hpo-HP.580012473\"> </a></td><td>Tongue atrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0003273<a name=\"hpo-HP.580003273\"> </a></td><td>Hip contracture</td></tr><tr><td style=\"white-space:nowrap\">HP:0006380<a name=\"hpo-HP.580006380\"> </a></td><td>Knee flexion contracture</td></tr><tr><td style=\"white-space:nowrap\">HP:0003752<a name=\"hpo-HP.580003752\"> </a></td><td>Episodic flaccid weakness</td></tr><tr><td style=\"white-space:nowrap\">HP:0100298<a name=\"hpo-HP.580100298\"> </a></td><td>Motheaten muscle fibers</td></tr><tr><td style=\"white-space:nowrap\">HP:0003693<a name=\"hpo-HP.580003693\"> </a></td><td>Distal amyotrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0002167<a name=\"hpo-HP.580002167\"> </a></td><td>Neurological speech impairment</td></tr><tr><td style=\"white-space:nowrap\">HP:0003388<a name=\"hpo-HP.580003388\"> </a></td><td>Easy fatigability</td></tr><tr><td style=\"white-space:nowrap\">HP:0001348<a name=\"hpo-HP.580001348\"> </a></td><td>Brisk reflexes</td></tr><tr><td style=\"white-space:nowrap\">HP:0003445<a name=\"hpo-HP.580003445\"> </a></td><td>EMG: neuropathic changes</td></tr><tr><td style=\"white-space:nowrap\">HP:0009063<a name=\"hpo-HP.580009063\"> </a></td><td>Progressive distal muscle weakness</td></tr><tr><td style=\"white-space:nowrap\">HP:0003720<a name=\"hpo-HP.580003720\"> </a></td><td>Generalized muscle hypertrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0002493<a name=\"hpo-HP.580002493\"> </a></td><td>Upper motor neuron dysfunction</td></tr><tr><td style=\"white-space:nowrap\">HP:0012448<a name=\"hpo-HP.580012448\"> </a></td><td>Delayed myelination</td></tr><tr><td style=\"white-space:nowrap\">HP:0001338<a name=\"hpo-HP.580001338\"> </a></td><td>Partial agenesis of the corpus callosum</td></tr><tr><td style=\"white-space:nowrap\">HP:0006879<a name=\"hpo-HP.580006879\"> </a></td><td>Pontocerebellar atrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0200101<a name=\"hpo-HP.580200101\"> </a></td><td>Decreased/absent ankle reflexes</td></tr><tr><td style=\"white-space:nowrap\">HP:0009020<a name=\"hpo-HP.580009020\"> </a></td><td>Exercise-induced muscle fatigue</td></tr><tr><td style=\"white-space:nowrap\">HP:0002067<a name=\"hpo-HP.580002067\"> </a></td><td>Bradykinesia</td></tr><tr><td style=\"white-space:nowrap\">HP:0012751<a name=\"hpo-HP.580012751\"> </a></td><td>Abnormal basal ganglia MRI signal intensity</td></tr><tr><td style=\"white-space:nowrap\">HP:0003355<a name=\"hpo-HP.580003355\"> </a></td><td>Aminoaciduria</td></tr><tr><td style=\"white-space:nowrap\">HP:0012450<a name=\"hpo-HP.580012450\"> </a></td><td>Chronic constipation</td></tr><tr><td style=\"white-space:nowrap\">HP:0011834<a name=\"hpo-HP.580011834\"> </a></td><td>Moyamoya phenomenon</td></tr><tr><td style=\"white-space:nowrap\">HP:0001297<a name=\"hpo-HP.580001297\"> </a></td><td>Stroke</td></tr><tr><td style=\"white-space:nowrap\">HP:0200049<a name=\"hpo-HP.580200049\"> </a></td><td>Upper limb hypertonia</td></tr><tr><td style=\"white-space:nowrap\">HP:0008981<a name=\"hpo-HP.580008981\"> </a></td><td>Calf muscle hypertrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0006785<a name=\"hpo-HP.580006785\"> </a></td><td>Limb-girdle muscular dystrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0006957<a name=\"hpo-HP.580006957\"> </a></td><td>Loss of ability to walk</td></tr><tr><td style=\"white-space:nowrap\">HP:0030098<a name=\"hpo-HP.580030098\"> </a></td><td>Reduced muscle dystrophin expression</td></tr><tr><td style=\"white-space:nowrap\">HP:0030115<a name=\"hpo-HP.580030115\"> </a></td><td>Reduced muscle fiber dysferlin</td></tr><tr><td style=\"white-space:nowrap\">HP:0002058<a name=\"hpo-HP.580002058\"> </a></td><td>Myopathic facies</td></tr><tr><td style=\"white-space:nowrap\">HP:0007858<a name=\"hpo-HP.580007858\"> </a></td><td>Chorioretinal lacunae</td></tr><tr><td style=\"white-space:nowrap\">HP:0006657<a name=\"hpo-HP.580006657\"> </a></td><td>Hypoplasia of first ribs</td></tr><tr><td style=\"white-space:nowrap\">HP:0007165<a name=\"hpo-HP.580007165\"> </a></td><td>Periventricular heterotopia</td></tr><tr><td style=\"white-space:nowrap\">HP:0009779<a name=\"hpo-HP.580009779\"> </a></td><td>3-4 toe syndactyly</td></tr><tr><td style=\"white-space:nowrap\">HP:0010665<a name=\"hpo-HP.580010665\"> </a></td><td>Bilateral coxa valga</td></tr><tr><td style=\"white-space:nowrap\">HP:0007598<a name=\"hpo-HP.580007598\"> </a></td><td>Bilateral single transverse palmar creases</td></tr><tr><td style=\"white-space:nowrap\">HP:0006101<a name=\"hpo-HP.580006101\"> </a></td><td>Finger syndactyly</td></tr><tr><td style=\"white-space:nowrap\">HP:0010511<a name=\"hpo-HP.580010511\"> </a></td><td>Long toe</td></tr><tr><td style=\"white-space:nowrap\">HP:0002370<a name=\"hpo-HP.580002370\"> </a></td><td>Poor coordination</td></tr><tr><td style=\"white-space:nowrap\">HP:0000480<a name=\"hpo-HP.580000480\"> </a></td><td>Retinal coloboma</td></tr><tr><td style=\"white-space:nowrap\">HP:0001770<a name=\"hpo-HP.580001770\"> </a></td><td>Toe syndactyly</td></tr><tr><td style=\"white-space:nowrap\">HP:0010851<a name=\"hpo-HP.580010851\"> </a></td><td>EEG with burst suppression</td></tr><tr><td style=\"white-space:nowrap\">HP:0002791<a name=\"hpo-HP.580002791\"> </a></td><td>Hypoventilation</td></tr><tr><td style=\"white-space:nowrap\">HP:0040075<a name=\"hpo-HP.580040075\"> </a></td><td>Hypopituitarism</td></tr><tr><td style=\"white-space:nowrap\">HP:0012506<a name=\"hpo-HP.580012506\"> </a></td><td>Small pituitary gland</td></tr><tr><td style=\"white-space:nowrap\">HP:0000538<a name=\"hpo-HP.580000538\"> </a></td><td>Pseudopapilledema</td></tr><tr><td style=\"white-space:nowrap\">HP:0012717<a name=\"hpo-HP.580012717\"> </a></td><td>Severe conductive hearing impairment</td></tr><tr><td style=\"white-space:nowrap\">HP:0001370<a name=\"hpo-HP.580001370\"> </a></td><td>Rheumatoid arthritis</td></tr><tr><td style=\"white-space:nowrap\">HP:0000016<a name=\"hpo-HP.580000016\"> </a></td><td>Urinary retention</td></tr><tr><td style=\"white-space:nowrap\">HP:0012537<a name=\"hpo-HP.580012537\"> </a></td><td>Food intolerance</td></tr><tr><td style=\"white-space:nowrap\">HP:0011297<a name=\"hpo-HP.580011297\"> </a></td><td>Abnormal digit morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0001273<a name=\"hpo-HP.580001273\"> </a></td><td>Abnormal corpus callosum morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0030148<a name=\"hpo-HP.580030148\"> </a></td><td>Heart murmur</td></tr><tr><td style=\"white-space:nowrap\">HP:0045018<a name=\"hpo-HP.580045018\"> </a></td><td>Partial duplication of eyebrows</td></tr><tr><td style=\"white-space:nowrap\">HP:0008998<a name=\"hpo-HP.580008998\"> </a></td><td>Pectoralis hypoplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001707<a name=\"hpo-HP.580001707\"> </a></td><td>Abnormal right ventricle morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0001540<a name=\"hpo-HP.580001540\"> </a></td><td>Diastasis recti</td></tr><tr><td style=\"white-space:nowrap\">HP:0100693<a name=\"hpo-HP.580100693\"> </a></td><td>Iridodonesis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002265<a name=\"hpo-HP.580002265\"> </a></td><td>Large fleshy ears</td></tr><tr><td style=\"white-space:nowrap\">HP:0001132<a name=\"hpo-HP.580001132\"> </a></td><td>Lens subluxation</td></tr><tr><td style=\"white-space:nowrap\">HP:0004927<a name=\"hpo-HP.580004927\"> </a></td><td>Pulmonary artery dilatation</td></tr><tr><td style=\"white-space:nowrap\">HP:0005619<a name=\"hpo-HP.580005619\"> </a></td><td>Thoracolumbar kyphosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0008619<a name=\"hpo-HP.580008619\"> </a></td><td>Bilateral sensorineural hearing impairment</td></tr><tr><td style=\"white-space:nowrap\">HP:0001045<a name=\"hpo-HP.580001045\"> </a></td><td>Vitiligo</td></tr><tr><td style=\"white-space:nowrap\">HP:0009124<a name=\"hpo-HP.580009124\"> </a></td><td>Abnormal adipose tissue morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0002979<a name=\"hpo-HP.580002979\"> </a></td><td>Bowing of the legs</td></tr><tr><td style=\"white-space:nowrap\">HP:0000455<a name=\"hpo-HP.580000455\"> </a></td><td>Broad nasal tip</td></tr><tr><td style=\"white-space:nowrap\">HP:0001007<a name=\"hpo-HP.580001007\"> </a></td><td>Hirsutism</td></tr><tr><td style=\"white-space:nowrap\">HP:0010314<a name=\"hpo-HP.580010314\"> </a></td><td>Premature thelarche</td></tr><tr><td style=\"white-space:nowrap\">HP:0000075<a name=\"hpo-HP.580000075\"> </a></td><td>Renal duplication</td></tr><tr><td style=\"white-space:nowrap\">HP:0000368<a name=\"hpo-HP.580000368\"> </a></td><td>Low-set, posteriorly rotated ears</td></tr><tr><td style=\"white-space:nowrap\">HP:0001052<a name=\"hpo-HP.580001052\"> </a></td><td>Nevus flammeus</td></tr><tr><td style=\"white-space:nowrap\">HP:0200048<a name=\"hpo-HP.580200048\"> </a></td><td>Cyanotic episode</td></tr><tr><td style=\"white-space:nowrap\">HP:0001902<a name=\"hpo-HP.580001902\"> </a></td><td>Giant platelets</td></tr><tr><td style=\"white-space:nowrap\">HP:0030043<a name=\"hpo-HP.580030043\"> </a></td><td>Hip subluxation</td></tr><tr><td style=\"white-space:nowrap\">HP:0002938<a name=\"hpo-HP.580002938\"> </a></td><td>Lumbar hyperlordosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0030084<a name=\"hpo-HP.580030084\"> </a></td><td>Clinodactyly</td></tr><tr><td style=\"white-space:nowrap\">HP:0005560<a name=\"hpo-HP.580005560\"> </a></td><td>Imbalanced hemoglobin synthesis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001539<a name=\"hpo-HP.580001539\"> </a></td><td>Omphalocele</td></tr><tr><td style=\"white-space:nowrap\">HP:0009778<a name=\"hpo-HP.580009778\"> </a></td><td>Short thumb</td></tr><tr><td style=\"white-space:nowrap\">HP:0002277<a name=\"hpo-HP.580002277\"> </a></td><td>Horner syndrome</td></tr><tr><td style=\"white-space:nowrap\">HP:0011701<a name=\"hpo-HP.580011701\"> </a></td><td>Multifocal atrial tachycardia</td></tr><tr><td style=\"white-space:nowrap\">HP:0005274<a name=\"hpo-HP.580005274\"> </a></td><td>Prominent nasal tip</td></tr><tr><td style=\"white-space:nowrap\">HP:0001262<a name=\"hpo-HP.580001262\"> </a></td><td>Excessive daytime somnolence</td></tr><tr><td style=\"white-space:nowrap\">HP:0001285<a name=\"hpo-HP.580001285\"> </a></td><td>Spastic tetraparesis</td></tr><tr><td style=\"white-space:nowrap\">HP:0012171<a name=\"hpo-HP.580012171\"> </a></td><td>Stereotypical hand wringing</td></tr><tr><td style=\"white-space:nowrap\">HP:0002518<a name=\"hpo-HP.580002518\"> </a></td><td>Abnormality of the periventricular white matter</td></tr><tr><td style=\"white-space:nowrap\">HP:0005692<a name=\"hpo-HP.580005692\"> </a></td><td>Joint hyperflexibility</td></tr><tr><td style=\"white-space:nowrap\">HP:0007440<a name=\"hpo-HP.580007440\"> </a></td><td>Generalized hyperpigmentation</td></tr><tr><td style=\"white-space:nowrap\">HP:0001805<a name=\"hpo-HP.580001805\"> </a></td><td>Onychogryposis</td></tr><tr><td style=\"white-space:nowrap\">HP:0011945<a name=\"hpo-HP.580011945\"> </a></td><td>Bronchiolitis obliterans organizing pneumonia</td></tr><tr><td style=\"white-space:nowrap\">HP:0003763<a name=\"hpo-HP.580003763\"> </a></td><td>Bruxism</td></tr><tr><td style=\"white-space:nowrap\">HP:0010500<a name=\"hpo-HP.580010500\"> </a></td><td>Hyperextensibility of the knee</td></tr><tr><td style=\"white-space:nowrap\">HP:0040115<a name=\"hpo-HP.580040115\"> </a></td><td>Abnormality of the Eustachian tube</td></tr><tr><td style=\"white-space:nowrap\">HP:0008751<a name=\"hpo-HP.580008751\"> </a></td><td>Laryngeal cleft</td></tr><tr><td style=\"white-space:nowrap\">HP:0000403<a name=\"hpo-HP.580000403\"> </a></td><td>Recurrent otitis media</td></tr><tr><td style=\"white-space:nowrap\">HP:0001787<a name=\"hpo-HP.580001787\"> </a></td><td>Abnormal delivery</td></tr><tr><td style=\"white-space:nowrap\">HP:0002571<a name=\"hpo-HP.580002571\"> </a></td><td>Achalasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002615<a name=\"hpo-HP.580002615\"> </a></td><td>Hypotension</td></tr><tr><td style=\"white-space:nowrap\">HP:0003550<a name=\"hpo-HP.580003550\"> </a></td><td>Predominantly lower limb lymphedema</td></tr><tr><td style=\"white-space:nowrap\">HP:0030363<a name=\"hpo-HP.580030363\"> </a></td><td>Primary Caesarian section</td></tr><tr><td style=\"white-space:nowrap\">HP:0001727<a name=\"hpo-HP.580001727\"> </a></td><td>Thromboembolic stroke</td></tr><tr><td style=\"white-space:nowrap\">HP:0100603<a name=\"hpo-HP.580100603\"> </a></td><td>Toxemia of pregnancy</td></tr><tr><td style=\"white-space:nowrap\">HP:0010836<a name=\"hpo-HP.580010836\"> </a></td><td>Abnormal circulating copper concentration</td></tr><tr><td style=\"white-space:nowrap\">HP:0000356<a name=\"hpo-HP.580000356\"> </a></td><td>Abnormality of the outer ear</td></tr><tr><td style=\"white-space:nowrap\">HP:0002197<a name=\"hpo-HP.580002197\"> </a></td><td>Generalized-onset seizure</td></tr><tr><td style=\"white-space:nowrap\">HP:0011436<a name=\"hpo-HP.580011436\"> </a></td><td>Abnormal maternal serum screening</td></tr><tr><td style=\"white-space:nowrap\">HP:0003517<a name=\"hpo-HP.580003517\"> </a></td><td>Birth length greater than 97th percentile</td></tr><tr><td style=\"white-space:nowrap\">HP:0003561<a name=\"hpo-HP.580003561\"> </a></td><td>Birth length less than 3rd percentile</td></tr><tr><td style=\"white-space:nowrap\">HP:0012188<a name=\"hpo-HP.580012188\"> </a></td><td>Hyperemesis gravidarum</td></tr><tr><td style=\"white-space:nowrap\">HP:0010519<a name=\"hpo-HP.580010519\"> </a></td><td>Increased fetal movement</td></tr><tr><td style=\"white-space:nowrap\">HP:0030244<a name=\"hpo-HP.580030244\"> </a></td><td>Maternal fever in pregnancy</td></tr><tr><td style=\"white-space:nowrap\">HP:0008071<a name=\"hpo-HP.580008071\"> </a></td><td>Maternal hypertension</td></tr><tr><td style=\"white-space:nowrap\">HP:0100622<a name=\"hpo-HP.580100622\"> </a></td><td>Maternal seizure</td></tr><tr><td style=\"white-space:nowrap\">HP:0011438<a name=\"hpo-HP.580011438\"> </a></td><td>Maternal teratogenic exposure</td></tr><tr><td style=\"white-space:nowrap\">HP:0001998<a name=\"hpo-HP.580001998\"> </a></td><td>Neonatal hypoglycemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0040187<a name=\"hpo-HP.580040187\"> </a></td><td>Neonatal sepsis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002033<a name=\"hpo-HP.580002033\"> </a></td><td>Poor suck</td></tr><tr><td style=\"white-space:nowrap\">HP:0006579<a name=\"hpo-HP.580006579\"> </a></td><td>Prolonged neonatal jaundice</td></tr><tr><td style=\"white-space:nowrap\">HP:0001724<a name=\"hpo-HP.580001724\"> </a></td><td>obsolete Aortic dilatation</td></tr><tr><td style=\"white-space:nowrap\">HP:0010621<a name=\"hpo-HP.580010621\"> </a></td><td>Cutaneous syndactyly of toes</td></tr><tr><td style=\"white-space:nowrap\">HP:0001880<a name=\"hpo-HP.580001880\"> </a></td><td>Eosinophilia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000162<a name=\"hpo-HP.580000162\"> </a></td><td>Glossoptosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0100578<a name=\"hpo-HP.580100578\"> </a></td><td>Lipoatrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0002562<a name=\"hpo-HP.580002562\"> </a></td><td>Low-set nipples</td></tr><tr><td style=\"white-space:nowrap\">HP:0012893<a name=\"hpo-HP.580012893\"> </a></td><td>Neck muscle hypertrophy</td></tr><tr><td style=\"white-space:nowrap\">HP:0001027<a name=\"hpo-HP.580001027\"> </a></td><td>Soft, doughy skin</td></tr><tr><td style=\"white-space:nowrap\">HP:0100738<a name=\"hpo-HP.580100738\"> </a></td><td>Abnormal eating behavior</td></tr><tr><td style=\"white-space:nowrap\">HP:0007328<a name=\"hpo-HP.580007328\"> </a></td><td>Impaired pain sensation</td></tr><tr><td style=\"white-space:nowrap\">HP:0002878<a name=\"hpo-HP.580002878\"> </a></td><td>Respiratory failure</td></tr><tr><td style=\"white-space:nowrap\">HP:0001776<a name=\"hpo-HP.580001776\"> </a></td><td>Bilateral talipes equinovarus</td></tr><tr><td style=\"white-space:nowrap\">HP:0001360<a name=\"hpo-HP.580001360\"> </a></td><td>Holoprosencephaly</td></tr><tr><td style=\"white-space:nowrap\">HP:0001973<a name=\"hpo-HP.580001973\"> </a></td><td>Autoimmune thrombocytopenia</td></tr><tr><td style=\"white-space:nowrap\">HP:0100749<a name=\"hpo-HP.580100749\"> </a></td><td>Chest pain</td></tr><tr><td style=\"white-space:nowrap\">HP:0012531<a name=\"hpo-HP.580012531\"> </a></td><td>Pain</td></tr><tr><td style=\"white-space:nowrap\">HP:0007585<a name=\"hpo-HP.580007585\"> </a></td><td>Skin fragility with non-scarring blistering</td></tr><tr><td style=\"white-space:nowrap\">HP:0002108<a name=\"hpo-HP.580002108\"> </a></td><td>Spontaneous pneumothorax</td></tr><tr><td style=\"white-space:nowrap\">HP:0006562<a name=\"hpo-HP.580006562\"> </a></td><td>Viral hepatitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0012647<a name=\"hpo-HP.580012647\"> </a></td><td>Abnormal inflammatory response</td></tr><tr><td style=\"white-space:nowrap\">HP:0012088<a name=\"hpo-HP.580012088\"> </a></td><td>Abnormal urinary odor</td></tr><tr><td style=\"white-space:nowrap\">HP:0011458<a name=\"hpo-HP.580011458\"> </a></td><td>Abdominal symptom</td></tr><tr><td style=\"white-space:nowrap\">HP:0002829<a name=\"hpo-HP.580002829\"> </a></td><td>Arthralgia</td></tr><tr><td style=\"white-space:nowrap\">HP:0010783<a name=\"hpo-HP.580010783\"> </a></td><td>Erythema</td></tr><tr><td style=\"white-space:nowrap\">HP:0010307<a name=\"hpo-HP.580010307\"> </a></td><td>Stridor</td></tr><tr><td style=\"white-space:nowrap\">HP:0001269<a name=\"hpo-HP.580001269\"> </a></td><td>Hemiparesis</td></tr><tr><td style=\"white-space:nowrap\">HP:0006532<a name=\"hpo-HP.580006532\"> </a></td><td>Recurrent pneumonia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002580<a name=\"hpo-HP.580002580\"> </a></td><td>Volvulus</td></tr><tr><td style=\"white-space:nowrap\">HP:0012387<a name=\"hpo-HP.580012387\"> </a></td><td>Bronchitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001266<a name=\"hpo-HP.580001266\"> </a></td><td>Choreoathetosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001531<a name=\"hpo-HP.580001531\"> </a></td><td>Failure to thrive in infancy</td></tr><tr><td style=\"white-space:nowrap\">HP:0011470<a name=\"hpo-HP.580011470\"> </a></td><td>Nasogastric tube feeding in infancy</td></tr><tr><td style=\"white-space:nowrap\">HP:0001361<a name=\"hpo-HP.580001361\"> </a></td><td>Nystagmus-induced head nodding</td></tr><tr><td style=\"white-space:nowrap\">HP:0001997<a name=\"hpo-HP.580001997\"> </a></td><td>Gout</td></tr><tr><td style=\"white-space:nowrap\">HP:0000965<a name=\"hpo-HP.580000965\"> </a></td><td>Cutis marmorata</td></tr><tr><td style=\"white-space:nowrap\">HP:0010316<a name=\"hpo-HP.580010316\"> </a></td><td>Ebstein anomaly of the tricuspid valve</td></tr><tr><td style=\"white-space:nowrap\">HP:0010543<a name=\"hpo-HP.580010543\"> </a></td><td>Opsoclonus</td></tr><tr><td style=\"white-space:nowrap\">HP:0007704<a name=\"hpo-HP.580007704\"> </a></td><td>Paroxysmal involuntary eye movements</td></tr><tr><td style=\"white-space:nowrap\">HP:0030364<a name=\"hpo-HP.580030364\"> </a></td><td>Secondary Caesarian section</td></tr><tr><td style=\"white-space:nowrap\">HP:0007738<a name=\"hpo-HP.580007738\"> </a></td><td>Uncontrolled eye movements</td></tr><tr><td style=\"white-space:nowrap\">HP:0030366<a name=\"hpo-HP.580030366\"> </a></td><td>Delivery by Odon device</td></tr><tr><td style=\"white-space:nowrap\">HP:0011411<a name=\"hpo-HP.580011411\"> </a></td><td>Forceps delivery</td></tr><tr><td style=\"white-space:nowrap\">HP:0030369<a name=\"hpo-HP.580030369\"> </a></td><td>Induced vaginal delivery</td></tr><tr><td style=\"white-space:nowrap\">HP:0005268<a name=\"hpo-HP.580005268\"> </a></td><td>Spontaneous abortion</td></tr><tr><td style=\"white-space:nowrap\">HP:0030365<a name=\"hpo-HP.580030365\"> </a></td><td>Vaginal birth after Caesarian</td></tr><tr><td style=\"white-space:nowrap\">HP:0011412<a name=\"hpo-HP.580011412\"> </a></td><td>Ventouse delivery</td></tr><tr><td style=\"white-space:nowrap\">HP:0002572<a name=\"hpo-HP.580002572\"> </a></td><td>Episodic vomiting</td></tr><tr><td style=\"white-space:nowrap\">HP:0030350<a name=\"hpo-HP.580030350\"> </a></td><td>Erythematous papule</td></tr><tr><td style=\"white-space:nowrap\">HP:0001386<a name=\"hpo-HP.580001386\"> </a></td><td>Joint swelling</td></tr><tr><td style=\"white-space:nowrap\">HP:0000147<a name=\"hpo-HP.580000147\"> </a></td><td>Polycystic ovaries</td></tr><tr><td style=\"white-space:nowrap\">HP:0012412<a name=\"hpo-HP.580012412\"> </a></td><td>Premature adrenarche</td></tr><tr><td style=\"white-space:nowrap\">HP:0004411<a name=\"hpo-HP.580004411\"> </a></td><td>Deviated nasal septum</td></tr><tr><td style=\"white-space:nowrap\">HP:0040183<a name=\"hpo-HP.580040183\"> </a></td><td>Encopresis</td></tr><tr><td style=\"white-space:nowrap\">HP:0100507<a name=\"hpo-HP.580100507\"> </a></td><td>Reduced blood folate concentration</td></tr><tr><td style=\"white-space:nowrap\">HP:0007011<a name=\"hpo-HP.580007011\"> </a></td><td>Fourth cranial nerve palsy</td></tr><tr><td style=\"white-space:nowrap\">HP:0000375<a name=\"hpo-HP.580000375\"> </a></td><td>Abnormal cochlea morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0009911<a name=\"hpo-HP.580009911\"> </a></td><td>Abnormal temporal bone morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0000081<a name=\"hpo-HP.580000081\"> </a></td><td>Duplicated collecting system</td></tr><tr><td style=\"white-space:nowrap\">HP:0006894<a name=\"hpo-HP.580006894\"> </a></td><td>Hypoplastic olfactory lobes</td></tr><tr><td style=\"white-space:nowrap\">HP:0011380<a name=\"hpo-HP.580011380\"> </a></td><td>Morphological abnormality of the semicircular canal</td></tr><tr><td style=\"white-space:nowrap\">HP:0000110<a name=\"hpo-HP.580000110\"> </a></td><td>Renal dysplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0030025<a name=\"hpo-HP.580030025\"> </a></td><td>Auricular pit</td></tr><tr><td style=\"white-space:nowrap\">HP:0010044<a name=\"hpo-HP.580010044\"> </a></td><td>Short 4th metacarpal</td></tr><tr><td style=\"white-space:nowrap\">HP:0010047<a name=\"hpo-HP.580010047\"> </a></td><td>Short 5th metacarpal</td></tr><tr><td style=\"white-space:nowrap\">HP:0000201<a name=\"hpo-HP.580000201\"> </a></td><td>Pierre-Robin sequence</td></tr><tr><td style=\"white-space:nowrap\">HP:0100837<a name=\"hpo-HP.580100837\"> </a></td><td>Atrophodermia vermiculata</td></tr><tr><td style=\"white-space:nowrap\">HP:0002673<a name=\"hpo-HP.580002673\"> </a></td><td>Coxa valga</td></tr><tr><td style=\"white-space:nowrap\">HP:0001476<a name=\"hpo-HP.580001476\"> </a></td><td>Delayed closure of the anterior fontanelle</td></tr><tr><td style=\"white-space:nowrap\">HP:0011069<a name=\"hpo-HP.580011069\"> </a></td><td>Increased number of teeth</td></tr><tr><td style=\"white-space:nowrap\">HP:0009879<a name=\"hpo-HP.580009879\"> </a></td><td>Simplified gyral pattern</td></tr><tr><td style=\"white-space:nowrap\">HP:0006315<a name=\"hpo-HP.580006315\"> </a></td><td>Single median maxillary incisor</td></tr><tr><td style=\"white-space:nowrap\">HP:0001194<a name=\"hpo-HP.580001194\"> </a></td><td>Abnormalities of placenta or umbilical cord</td></tr><tr><td style=\"white-space:nowrap\">HP:0100767<a name=\"hpo-HP.580100767\"> </a></td><td>Abnormal placenta morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0006543<a name=\"hpo-HP.580006543\"> </a></td><td>Cardiorespiratory arrest</td></tr><tr><td style=\"white-space:nowrap\">HP:0003074<a name=\"hpo-HP.580003074\"> </a></td><td>Hyperglycemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000842<a name=\"hpo-HP.580000842\"> </a></td><td>Hyperinsulinemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0011951<a name=\"hpo-HP.580011951\"> </a></td><td>Aspiration pneumonia</td></tr><tr><td style=\"white-space:nowrap\">HP:0006528<a name=\"hpo-HP.580006528\"> </a></td><td>Chronic lung disease</td></tr><tr><td style=\"white-space:nowrap\">HP:0002383<a name=\"hpo-HP.580002383\"> </a></td><td>Encephalitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0000388<a name=\"hpo-HP.580000388\"> </a></td><td>Otitis media</td></tr><tr><td style=\"white-space:nowrap\">HP:0002530<a name=\"hpo-HP.580002530\"> </a></td><td>Axial dystonia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002780<a name=\"hpo-HP.580002780\"> </a></td><td>Bronchomalacia</td></tr><tr><td style=\"white-space:nowrap\">HP:0008755<a name=\"hpo-HP.580008755\"> </a></td><td>Laryngotracheomalacia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000308<a name=\"hpo-HP.580000308\"> </a></td><td>Microretrognathia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002786<a name=\"hpo-HP.580002786\"> </a></td><td>Tracheobronchomalacia</td></tr><tr><td style=\"white-space:nowrap\">HP:0012389<a name=\"hpo-HP.580012389\"> </a></td><td>Appendicular hypotonia</td></tr><tr><td style=\"white-space:nowrap\">HP:0011323<a name=\"hpo-HP.580011323\"> </a></td><td>Cleft of chin</td></tr><tr><td style=\"white-space:nowrap\">HP:0000417<a name=\"hpo-HP.580000417\"> </a></td><td>Slender nose</td></tr><tr><td style=\"white-space:nowrap\">HP:0001863<a name=\"hpo-HP.580001863\"> </a></td><td>Toe clinodactyly</td></tr><tr><td style=\"white-space:nowrap\">HP:0008386<a name=\"hpo-HP.580008386\"> </a></td><td>Aplasia/Hypoplasia of the nails</td></tr><tr><td style=\"white-space:nowrap\">HP:0006989<a name=\"hpo-HP.580006989\"> </a></td><td>Dysplastic corpus callosum</td></tr><tr><td style=\"white-space:nowrap\">HP:0100954<a name=\"hpo-HP.580100954\"> </a></td><td>Open operculum</td></tr><tr><td style=\"white-space:nowrap\">HP:0004482<a name=\"hpo-HP.580004482\"> </a></td><td>Relative macrocephaly</td></tr><tr><td style=\"white-space:nowrap\">HP:3000033<a name=\"hpo-HP.583000033\"> </a></td><td>Abnormal nasopharyngeal adenoid morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0009062<a name=\"hpo-HP.580009062\"> </a></td><td>Infantile axial hypotonia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002189<a name=\"hpo-HP.580002189\"> </a></td><td>obsolete Excessive daytime sleepiness</td></tr><tr><td style=\"white-space:nowrap\">HP:0002141<a name=\"hpo-HP.580002141\"> </a></td><td>Gait imbalance</td></tr><tr><td style=\"white-space:nowrap\">HP:0012734<a name=\"hpo-HP.580012734\"> </a></td><td>Ketotic hypoglycemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0005968<a name=\"hpo-HP.580005968\"> </a></td><td>Temperature instability</td></tr><tr><td style=\"white-space:nowrap\">HP:0012538<a name=\"hpo-HP.580012538\"> </a></td><td>Gluten intolerance</td></tr><tr><td style=\"white-space:nowrap\">HP:0000979<a name=\"hpo-HP.580000979\"> </a></td><td>Purpura</td></tr><tr><td style=\"white-space:nowrap\">HP:0001988<a name=\"hpo-HP.580001988\"> </a></td><td>Recurrent hypoglycemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001488<a name=\"hpo-HP.580001488\"> </a></td><td>Bilateral ptosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0011229<a name=\"hpo-HP.580011229\"> </a></td><td>Broad eyebrow</td></tr><tr><td style=\"white-space:nowrap\">HP:0004440<a name=\"hpo-HP.580004440\"> </a></td><td>Coronal craniosynostosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0004453<a name=\"hpo-HP.580004453\"> </a></td><td>Overfolding of the superior helices</td></tr><tr><td style=\"white-space:nowrap\">HP:0012547<a name=\"hpo-HP.580012547\"> </a></td><td>Abnormal involuntary eye movements</td></tr><tr><td style=\"white-space:nowrap\">HP:0100814<a name=\"hpo-HP.580100814\"> </a></td><td>Blue nevus</td></tr><tr><td style=\"white-space:nowrap\">HP:0010751<a name=\"hpo-HP.580010751\"> </a></td><td>Dimple chin</td></tr><tr><td style=\"white-space:nowrap\">HP:0007087<a name=\"hpo-HP.580007087\"> </a></td><td>obsolete Involuntary jerking movements</td></tr><tr><td style=\"white-space:nowrap\">HP:0012498<a name=\"hpo-HP.580012498\"> </a></td><td>Nuchal cord</td></tr><tr><td style=\"white-space:nowrap\">HP:0002472<a name=\"hpo-HP.580002472\"> </a></td><td>Small cerebral cortex</td></tr><tr><td style=\"white-space:nowrap\">HP:0100307<a name=\"hpo-HP.580100307\"> </a></td><td>Cerebellar hemisphere hypoplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002151<a name=\"hpo-HP.580002151\"> </a></td><td>Increased serum lactate</td></tr><tr><td style=\"white-space:nowrap\">HP:0001698<a name=\"hpo-HP.580001698\"> </a></td><td>Pericardial effusion</td></tr><tr><td style=\"white-space:nowrap\">HP:0006903<a name=\"hpo-HP.580006903\"> </a></td><td>Congenital peripheral neuropathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0006895<a name=\"hpo-HP.580006895\"> </a></td><td>Lower limb hypertonia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002744<a name=\"hpo-HP.580002744\"> </a></td><td>Bilateral cleft lip and palate</td></tr><tr><td style=\"white-space:nowrap\">HP:0010664<a name=\"hpo-HP.580010664\"> </a></td><td>Fusion of the left and right thalami</td></tr><tr><td style=\"white-space:nowrap\">HP:0000327<a name=\"hpo-HP.580000327\"> </a></td><td>Hypoplasia of the maxilla</td></tr><tr><td style=\"white-space:nowrap\">HP:0000474<a name=\"hpo-HP.580000474\"> </a></td><td>Thickened nuchal skin fold</td></tr><tr><td style=\"white-space:nowrap\">HP:0000105<a name=\"hpo-HP.580000105\"> </a></td><td>Enlarged kidney</td></tr><tr><td style=\"white-space:nowrap\">HP:0000113<a name=\"hpo-HP.580000113\"> </a></td><td>Polycystic kidney dysplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000104<a name=\"hpo-HP.580000104\"> </a></td><td>Renal agenesis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001362<a name=\"hpo-HP.580001362\"> </a></td><td>Calvarial skull defect</td></tr><tr><td style=\"white-space:nowrap\">HP:0008245<a name=\"hpo-HP.580008245\"> </a></td><td>Pituitary hypothyroidism</td></tr><tr><td style=\"white-space:nowrap\">HP:0001552<a name=\"hpo-HP.580001552\"> </a></td><td>Barrel-shaped chest</td></tr><tr><td style=\"white-space:nowrap\">HP:0006297<a name=\"hpo-HP.580006297\"> </a></td><td>Hypoplasia of dental enamel</td></tr><tr><td style=\"white-space:nowrap\">HP:0100023<a name=\"hpo-HP.580100023\"> </a></td><td>Recurrent hand flapping</td></tr><tr><td style=\"white-space:nowrap\">HP:0005518<a name=\"hpo-HP.580005518\"> </a></td><td>Increased mean corpuscular volume</td></tr><tr><td style=\"white-space:nowrap\">HP:0012418<a name=\"hpo-HP.580012418\"> </a></td><td>Hypoxemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0100259<a name=\"hpo-HP.580100259\"> </a></td><td>Postaxial polydactyly</td></tr><tr><td style=\"white-space:nowrap\">HP:0010814<a name=\"hpo-HP.580010814\"> </a></td><td>Abnormal position of hair whorl</td></tr><tr><td style=\"white-space:nowrap\">HP:0003764<a name=\"hpo-HP.580003764\"> </a></td><td>Nevus</td></tr><tr><td style=\"white-space:nowrap\">HP:0000445<a name=\"hpo-HP.580000445\"> </a></td><td>Wide nose</td></tr><tr><td style=\"white-space:nowrap\">HP:0010677<a name=\"hpo-HP.580010677\"> </a></td><td>Enuresis nocturna</td></tr><tr><td style=\"white-space:nowrap\">HP:0001510<a name=\"hpo-HP.580001510\"> </a></td><td>Growth delay</td></tr><tr><td style=\"white-space:nowrap\">HP:0012428<a name=\"hpo-HP.580012428\"> </a></td><td>Prominent calcaneus</td></tr><tr><td style=\"white-space:nowrap\">HP:0012471<a name=\"hpo-HP.580012471\"> </a></td><td>Thick vermilion border</td></tr><tr><td style=\"white-space:nowrap\">HP:0007110<a name=\"hpo-HP.580007110\"> </a></td><td>Central hypoventilation</td></tr><tr><td style=\"white-space:nowrap\">HP:0010614<a name=\"hpo-HP.580010614\"> </a></td><td>Fibroma</td></tr><tr><td style=\"white-space:nowrap\">HP:0001034<a name=\"hpo-HP.580001034\"> </a></td><td>Hypermelanotic macule</td></tr><tr><td style=\"white-space:nowrap\">HP:0011365<a name=\"hpo-HP.580011365\"> </a></td><td>Patchy hypopigmentation of hair</td></tr><tr><td style=\"white-space:nowrap\">HP:0001920<a name=\"hpo-HP.580001920\"> </a></td><td>Renal artery stenosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002828<a name=\"hpo-HP.580002828\"> </a></td><td>Multiple joint contractures</td></tr><tr><td style=\"white-space:nowrap\">HP:0002144<a name=\"hpo-HP.580002144\"> </a></td><td>Tethered cord</td></tr><tr><td style=\"white-space:nowrap\">HP:0010964<a name=\"hpo-HP.580010964\"> </a></td><td>Abnormal circulating long-chain fatty-acid concentration</td></tr><tr><td style=\"white-space:nowrap\">HP:0010536<a name=\"hpo-HP.580010536\"> </a></td><td>Central sleep apnea</td></tr><tr><td style=\"white-space:nowrap\">HP:0011262<a name=\"hpo-HP.580011262\"> </a></td><td>Crimped helix</td></tr><tr><td style=\"white-space:nowrap\">HP:0040079<a name=\"hpo-HP.580040079\"> </a></td><td>Irregular dentition</td></tr><tr><td style=\"white-space:nowrap\">HP:0011481<a name=\"hpo-HP.580011481\"> </a></td><td>Abnormal lacrimal duct morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0000220<a name=\"hpo-HP.580000220\"> </a></td><td>Velopharyngeal insufficiency</td></tr><tr><td style=\"white-space:nowrap\">HP:0002153<a name=\"hpo-HP.580002153\"> </a></td><td>Hyperkalemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002148<a name=\"hpo-HP.580002148\"> </a></td><td>Hypophosphatemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0012621<a name=\"hpo-HP.580012621\"> </a></td><td>Persistent cloaca</td></tr><tr><td style=\"white-space:nowrap\">HP:0000867<a name=\"hpo-HP.580000867\"> </a></td><td>Secondary hyperparathyroidism</td></tr><tr><td style=\"white-space:nowrap\">HP:0003762<a name=\"hpo-HP.580003762\"> </a></td><td>Uterus didelphys</td></tr><tr><td style=\"white-space:nowrap\">HP:0100512<a name=\"hpo-HP.580100512\"> </a></td><td>Low levels of vitamin D</td></tr><tr><td style=\"white-space:nowrap\">HP:0012156<a name=\"hpo-HP.580012156\"> </a></td><td>Hemophagocytosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0008209<a name=\"hpo-HP.580008209\"> </a></td><td>Premature ovarian insufficiency</td></tr><tr><td style=\"white-space:nowrap\">HP:0004349<a name=\"hpo-HP.580004349\"> </a></td><td>Reduced bone mineral density</td></tr><tr><td style=\"white-space:nowrap\">HP:0001924<a name=\"hpo-HP.580001924\"> </a></td><td>Sideroblastic anemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0011703<a name=\"hpo-HP.580011703\"> </a></td><td>Sinus tachycardia</td></tr><tr><td style=\"white-space:nowrap\">HP:0010609<a name=\"hpo-HP.580010609\"> </a></td><td>Skin tags</td></tr><tr><td style=\"white-space:nowrap\">HP:0002725<a name=\"hpo-HP.580002725\"> </a></td><td>Systemic lupus erythematosus</td></tr><tr><td style=\"white-space:nowrap\">HP:0003193<a name=\"hpo-HP.580003193\"> </a></td><td>Allergic rhinitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0006896<a name=\"hpo-HP.580006896\"> </a></td><td>Hypnopompic hallucinations</td></tr><tr><td style=\"white-space:nowrap\">HP:0002524<a name=\"hpo-HP.580002524\"> </a></td><td>Cataplexy</td></tr><tr><td style=\"white-space:nowrap\">HP:0005227<a name=\"hpo-HP.580005227\"> </a></td><td>Adenomatous colonic polyposis</td></tr><tr><td style=\"white-space:nowrap\">HP:0012173<a name=\"hpo-HP.580012173\"> </a></td><td>Orthostatic tachycardia</td></tr><tr><td style=\"white-space:nowrap\">HP:0001271<a name=\"hpo-HP.580001271\"> </a></td><td>Polyneuropathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0009120<a name=\"hpo-HP.580009120\"> </a></td><td>Aplasia/Hypoplasia involving the sinuses</td></tr><tr><td style=\"white-space:nowrap\">HP:0000625<a name=\"hpo-HP.580000625\"> </a></td><td>Eyelid coloboma</td></tr><tr><td style=\"white-space:nowrap\">HP:0009754<a name=\"hpo-HP.580009754\"> </a></td><td>Fibrous syngnathia</td></tr><tr><td style=\"white-space:nowrap\">HP:0012478<a name=\"hpo-HP.580012478\"> </a></td><td>Temporomandibular joint ankylosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001233<a name=\"hpo-HP.580001233\"> </a></td><td>2-3 finger syndactyly</td></tr><tr><td style=\"white-space:nowrap\">HP:0000811<a name=\"hpo-HP.580000811\"> </a></td><td>Abnormal external genitalia</td></tr><tr><td style=\"white-space:nowrap\">HP:0005120<a name=\"hpo-HP.580005120\"> </a></td><td>Abnormal cardiac atrium morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0008388<a name=\"hpo-HP.580008388\"> </a></td><td>Abnormal toenail morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0011467<a name=\"hpo-HP.580011467\"> </a></td><td>Absent gallbladder</td></tr><tr><td style=\"white-space:nowrap\">HP:0010760<a name=\"hpo-HP.580010760\"> </a></td><td>Absent toe</td></tr><tr><td style=\"white-space:nowrap\">HP:0001545<a name=\"hpo-HP.580001545\"> </a></td><td>Anteriorly placed anus</td></tr><tr><td style=\"white-space:nowrap\">HP:0001640<a name=\"hpo-HP.580001640\"> </a></td><td>Cardiomegaly</td></tr><tr><td style=\"white-space:nowrap\">HP:0002990<a name=\"hpo-HP.580002990\"> </a></td><td>Fibular aplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0004443<a name=\"hpo-HP.580004443\"> </a></td><td>Lambdoidal craniosynostosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0008569<a name=\"hpo-HP.580008569\"> </a></td><td>Microtia, second degree</td></tr><tr><td style=\"white-space:nowrap\">HP:0006277<a name=\"hpo-HP.580006277\"> </a></td><td>Pancreatic hyperplasia</td></tr><tr><td style=\"white-space:nowrap\">HP:0010445<a name=\"hpo-HP.580010445\"> </a></td><td>Primum atrial septal defect</td></tr><tr><td style=\"white-space:nowrap\">HP:0011640<a name=\"hpo-HP.580011640\"> </a></td><td>Single coronary artery origin</td></tr><tr><td style=\"white-space:nowrap\">HP:0011608<a name=\"hpo-HP.580011608\"> </a></td><td>Type II truncus arteriosus</td></tr><tr><td style=\"white-space:nowrap\">HP:0011327<a name=\"hpo-HP.580011327\"> </a></td><td>Posterior plagiocephaly</td></tr><tr><td style=\"white-space:nowrap\">HP:0007655<a name=\"hpo-HP.580007655\"> </a></td><td>Eversion of lateral third of lower eyelids</td></tr><tr><td style=\"white-space:nowrap\">HP:0010747<a name=\"hpo-HP.580010747\"> </a></td><td>Medial flaring of the eyebrow</td></tr><tr><td style=\"white-space:nowrap\">HP:0005957<a name=\"hpo-HP.580005957\"> </a></td><td>Breathing dysregulation</td></tr><tr><td style=\"white-space:nowrap\">HP:0000992<a name=\"hpo-HP.580000992\"> </a></td><td>Cutaneous photosensitivity</td></tr><tr><td style=\"white-space:nowrap\">HP:0011995<a name=\"hpo-HP.580011995\"> </a></td><td>Atrial septal dilatation</td></tr><tr><td style=\"white-space:nowrap\">HP:0000377<a name=\"hpo-HP.580000377\"> </a></td><td>Abnormality of the pinna</td></tr><tr><td style=\"white-space:nowrap\">HP:0011266<a name=\"hpo-HP.580011266\"> </a></td><td>Microtia, first degree</td></tr><tr><td style=\"white-space:nowrap\">HP:0012650<a name=\"hpo-HP.580012650\"> </a></td><td>Perisylvian polymicrogyria</td></tr><tr><td style=\"white-space:nowrap\">HP:0004970<a name=\"hpo-HP.580004970\"> </a></td><td>Ascending tubular aorta aneurysm</td></tr><tr><td style=\"white-space:nowrap\">HP:0008348<a name=\"hpo-HP.580008348\"> </a></td><td>Decreased circulating IgG2 level</td></tr><tr><td style=\"white-space:nowrap\">HP:0012115<a name=\"hpo-HP.580012115\"> </a></td><td>Hepatitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0006979<a name=\"hpo-HP.580006979\"> </a></td><td>Sleep-wake cycle disturbance</td></tr><tr><td style=\"white-space:nowrap\">HP:0008587<a name=\"hpo-HP.580008587\"> </a></td><td>Mild neurosensory hearing impairment</td></tr><tr><td style=\"white-space:nowrap\">HP:0006097<a name=\"hpo-HP.580006097\"> </a></td><td>3-4 finger syndactyly</td></tr><tr><td style=\"white-space:nowrap\">HP:0005263<a name=\"hpo-HP.580005263\"> </a></td><td>Gastritis</td></tr><tr><td style=\"white-space:nowrap\">HP:0200043<a name=\"hpo-HP.580200043\"> </a></td><td>Verrucae</td></tr><tr><td style=\"white-space:nowrap\">HP:0009600<a name=\"hpo-HP.580009600\"> </a></td><td>Flexion contracture of thumb</td></tr><tr><td style=\"white-space:nowrap\">HP:0010818<a name=\"hpo-HP.580010818\"> </a></td><td>Generalized tonic seizure</td></tr><tr><td style=\"white-space:nowrap\">HP:0002599<a name=\"hpo-HP.580002599\"> </a></td><td>Head titubation</td></tr><tr><td style=\"white-space:nowrap\">HP:0002090<a name=\"hpo-HP.580002090\"> </a></td><td>Pneumonia</td></tr><tr><td style=\"white-space:nowrap\">HP:0030423<a name=\"hpo-HP.580030423\"> </a></td><td>Splenic cyst</td></tr><tr><td style=\"white-space:nowrap\">HP:0030187<a name=\"hpo-HP.580030187\"> </a></td><td>Titubation</td></tr><tr><td style=\"white-space:nowrap\">HP:0002375<a name=\"hpo-HP.580002375\"> </a></td><td>Hypokinesia</td></tr><tr><td style=\"white-space:nowrap\">HP:0007166<a name=\"hpo-HP.580007166\"> </a></td><td>Paroxysmal dyskinesia</td></tr><tr><td style=\"white-space:nowrap\">HP:0003077<a name=\"hpo-HP.580003077\"> </a></td><td>Hyperlipidemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0000017<a name=\"hpo-HP.580000017\"> </a></td><td>Nocturia</td></tr><tr><td style=\"white-space:nowrap\">HP:0100555<a name=\"hpo-HP.580100555\"> </a></td><td>Asymmetric growth</td></tr><tr><td style=\"white-space:nowrap\">HP:0011847<a name=\"hpo-HP.580011847\"> </a></td><td>Giant cell tumor of bone</td></tr><tr><td style=\"white-space:nowrap\">HP:0000112<a name=\"hpo-HP.580000112\"> </a></td><td>Nephropathy</td></tr><tr><td style=\"white-space:nowrap\">HP:0000246<a name=\"hpo-HP.580000246\"> </a></td><td>Sinusitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001012<a name=\"hpo-HP.580001012\"> </a></td><td>Multiple lipomas</td></tr><tr><td style=\"white-space:nowrap\">HP:0000851<a name=\"hpo-HP.580000851\"> </a></td><td>Congenital hypothyroidism</td></tr><tr><td style=\"white-space:nowrap\">HP:0002345<a name=\"hpo-HP.580002345\"> </a></td><td>Action tremor</td></tr><tr><td style=\"white-space:nowrap\">HP:0002677<a name=\"hpo-HP.580002677\"> </a></td><td>Small foramen magnum</td></tr><tr><td style=\"white-space:nowrap\">HP:0011947<a name=\"hpo-HP.580011947\"> </a></td><td>Respiratory tract infection</td></tr><tr><td style=\"white-space:nowrap\">HP:0012151<a name=\"hpo-HP.580012151\"> </a></td><td>Hemothorax</td></tr><tr><td style=\"white-space:nowrap\">HP:0005988<a name=\"hpo-HP.580005988\"> </a></td><td>Congenital muscular torticollis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002329<a name=\"hpo-HP.580002329\"> </a></td><td>Drowsiness</td></tr><tr><td style=\"white-space:nowrap\">HP:0012395<a name=\"hpo-HP.580012395\"> </a></td><td>Seasonal allergy</td></tr><tr><td style=\"white-space:nowrap\">HP:0011679<a name=\"hpo-HP.580011679\"> </a></td><td>Tetralogy of Fallot with pulmonary stenosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0001864<a name=\"hpo-HP.580001864\"> </a></td><td>Clinodactyly of the 5th toe</td></tr><tr><td style=\"white-space:nowrap\">HP:0006934<a name=\"hpo-HP.580006934\"> </a></td><td>Congenital nystagmus</td></tr><tr><td style=\"white-space:nowrap\">HP:0100355<a name=\"hpo-HP.580100355\"> </a></td><td>Contractures of the distal interphalangeal joint of the 5th toe</td></tr><tr><td style=\"white-space:nowrap\">HP:0007894<a name=\"hpo-HP.580007894\"> </a></td><td>Hypopigmentation of the fundus</td></tr><tr><td style=\"white-space:nowrap\">HP:0012377<a name=\"hpo-HP.580012377\"> </a></td><td>Hemianopia</td></tr><tr><td style=\"white-space:nowrap\">HP:0002354<a name=\"hpo-HP.580002354\"> </a></td><td>Memory impairment</td></tr><tr><td style=\"white-space:nowrap\">HP:0000872<a name=\"hpo-HP.580000872\"> </a></td><td>Hashimoto thyroiditis</td></tr><tr><td style=\"white-space:nowrap\">HP:0002519<a name=\"hpo-HP.580002519\"> </a></td><td>Hypnagogic hallucinations</td></tr><tr><td style=\"white-space:nowrap\">HP:0010647<a name=\"hpo-HP.580010647\"> </a></td><td>Abnormal elasticity of skin</td></tr><tr><td style=\"white-space:nowrap\">HP:0002592<a name=\"hpo-HP.580002592\"> </a></td><td>Gastric ulcer</td></tr><tr><td style=\"white-space:nowrap\">HP:0004938<a name=\"hpo-HP.580004938\"> </a></td><td>Tortuous cerebral arteries</td></tr><tr><td style=\"white-space:nowrap\">HP:0004948<a name=\"hpo-HP.580004948\"> </a></td><td>Vascular tortuosity</td></tr><tr><td style=\"white-space:nowrap\">HP:0002516<a name=\"hpo-HP.580002516\"> </a></td><td>Increased intracranial pressure</td></tr><tr><td style=\"white-space:nowrap\">HP:0006460<a name=\"hpo-HP.580006460\"> </a></td><td>Increased laxity of ankles</td></tr><tr><td style=\"white-space:nowrap\">HP:0002317<a name=\"hpo-HP.580002317\"> </a></td><td>Unsteady gait</td></tr><tr><td style=\"white-space:nowrap\">HP:0000182<a name=\"hpo-HP.580000182\"> </a></td><td>Movement abnormality of the tongue</td></tr><tr><td style=\"white-space:nowrap\">HP:0009887<a name=\"hpo-HP.580009887\"> </a></td><td>Abnormality of hair pigmentation</td></tr><tr><td style=\"white-space:nowrap\">HP:0005824<a name=\"hpo-HP.580005824\"> </a></td><td>Clinodactyly of the 2nd toe</td></tr><tr><td style=\"white-space:nowrap\">HP:0002212<a name=\"hpo-HP.580002212\"> </a></td><td>Curly hair</td></tr><tr><td style=\"white-space:nowrap\">HP:0009803<a name=\"hpo-HP.580009803\"> </a></td><td>Short phalanx of finger</td></tr><tr><td style=\"white-space:nowrap\">HP:0000572<a name=\"hpo-HP.580000572\"> </a></td><td>Visual loss</td></tr><tr><td style=\"white-space:nowrap\">HP:0005216<a name=\"hpo-HP.580005216\"> </a></td><td>Impaired mastication</td></tr><tr><td style=\"white-space:nowrap\">HP:0000619<a name=\"hpo-HP.580000619\"> </a></td><td>Impaired convergence</td></tr><tr><td style=\"white-space:nowrap\">HP:0002403<a name=\"hpo-HP.580002403\"> </a></td><td>Positive Romberg sign</td></tr><tr><td style=\"white-space:nowrap\">HP:0008744<a name=\"hpo-HP.580008744\"> </a></td><td>Abnormal aryepiglottic fold morphology</td></tr><tr><td style=\"white-space:nowrap\">HP:0002374<a name=\"hpo-HP.580002374\"> </a></td><td>Diminished movement</td></tr><tr><td style=\"white-space:nowrap\">HP:0008277<a name=\"hpo-HP.580008277\"> </a></td><td>Abnormal blood zinc concentration</td></tr><tr><td style=\"white-space:nowrap\">HP:0012781<a name=\"hpo-HP.580012781\"> </a></td><td>Mid-frequency hearing loss</td></tr><tr><td style=\"white-space:nowrap\">HP:0100758<a name=\"hpo-HP.580100758\"> </a></td><td>Gangrene</td></tr><tr><td style=\"white-space:nowrap\">HP:0003256<a name=\"hpo-HP.580003256\"> </a></td><td>Abnormality of the coagulation cascade</td></tr><tr><td style=\"white-space:nowrap\">HP:0004387<a name=\"hpo-HP.580004387\"> </a></td><td>Enterocolitis</td></tr><tr><td style=\"white-space:nowrap\">HP:0011029<a name=\"hpo-HP.580011029\"> </a></td><td>Internal hemorrhage</td></tr><tr><td style=\"white-space:nowrap\">HP:0011649<a name=\"hpo-HP.580011649\"> </a></td><td>Patent ductus arteriosus after premature birth</td></tr><tr><td style=\"white-space:nowrap\">HP:0012050<a name=\"hpo-HP.580012050\"> </a></td><td>Anasarca</td></tr><tr><td style=\"white-space:nowrap\">HP:0001683<a name=\"hpo-HP.580001683\"> </a></td><td>Ectopia cordis</td></tr><tr><td style=\"white-space:nowrap\">HP:0011682<a name=\"hpo-HP.580011682\"> </a></td><td>Perimembranous ventricular septal defect</td></tr><tr><td style=\"white-space:nowrap\">HP:0010624<a name=\"hpo-HP.580010624\"> </a></td><td>Aplastic/hypoplastic toenail</td></tr><tr><td style=\"white-space:nowrap\">HP:0002705<a name=\"hpo-HP.580002705\"> </a></td><td>High, narrow palate</td></tr><tr><td style=\"white-space:nowrap\">HP:0011340<a name=\"hpo-HP.580011340\"> </a></td><td>Incomplete cleft of the upper lip</td></tr><tr><td style=\"white-space:nowrap\">HP:0011613<a name=\"hpo-HP.580011613\"> </a></td><td>Interrupted aortic arch type B</td></tr><tr><td style=\"white-space:nowrap\">HP:0006167<a name=\"hpo-HP.580006167\"> </a></td><td>Prominent proximal interphalangeal joints</td></tr><tr><td style=\"white-space:nowrap\">HP:0002918<a name=\"hpo-HP.580002918\"> </a></td><td>Hypermagnesemia</td></tr><tr><td style=\"white-space:nowrap\">HP:0011937<a name=\"hpo-HP.580011937\"> </a></td><td>Hypoplastic fifth toenail</td></tr><tr><td style=\"white-space:nowrap\">HP:0001067<a name=\"hpo-HP.580001067\"> </a></td><td>Neurofibromas</td></tr><tr><td style=\"white-space:nowrap\">HP:0011403<a name=\"hpo-HP.580011403\"> </a></td><td>Abnormal umbilical cord blood vessels</td></tr><tr><td style=\"white-space:nowrap\">HP:0003316<a name=\"hpo-HP.580003316\"> </a></td><td>Butterfly vertebrae</td></tr><tr><td style=\"white-space:nowrap\">HP:0002247<a name=\"hpo-HP.580002247\"> </a></td><td>Duodenal atresia</td></tr><tr><td style=\"white-space:nowrap\">HP:0008439<a name=\"hpo-HP.580008439\"> </a></td><td>Lumbar hemivertebrae</td></tr><tr><td style=\"white-space:nowrap\">HP:0011599<a name=\"hpo-HP.580011599\"> </a></td><td>Mesocardia</td></tr><tr><td style=\"white-space:nowrap\">HP:0008467<a name=\"hpo-HP.580008467\"> </a></td><td>Thoracic hemivertebrae</td></tr><tr><td style=\"white-space:nowrap\">HP:0004626<a name=\"hpo-HP.580004626\"> </a></td><td>Lumbar scoliosis</td></tr><tr><td style=\"white-space:nowrap\">HP:0006808<a name=\"hpo-HP.580006808\"> </a></td><td>Cerebral hypomyelination</td></tr><tr><td style=\"white-space:nowrap\">HP:0002926<a name=\"hpo-HP.580002926\"> </a></td><td>Abnormality of thyroid physiology</td></tr><tr><td style=\"white-space:nowrap\">HP:0007970<a name=\"hpo-HP.580007970\"> </a></td><td>Congenital ptosis</td></tr></table></div>"
  ]; # 
  fhir:CodeSystem.url [ fhir:value "http://purl.obolibrary.org/obo/hp.owl"]; # 
  fhir:CodeSystem.version [ fhir:value "0.2.0"]; # 
  fhir:CodeSystem.name [ fhir:value "HPO"]; # 
  fhir:CodeSystem.title [ fhir:value "Human Phenotype Ontology"]; # 
  fhir:CodeSystem.status [ fhir:value "draft"]; # 
  fhir:CodeSystem.experimental [ fhir:value "false"^^xsd:boolean]; # 
  fhir:CodeSystem.date [ fhir:value "2022-12-09T17:30:30+00:00"^^xsd:dateTime]; # 
  fhir:CodeSystem.publisher [ fhir:value "NCPI FHIR Working Group"]; # 
  fhir:CodeSystem.contact [
     fhir:index 0;
     fhir:ContactDetail.name [ fhir:value "NCPI FHIR Working Group" ];
     fhir:ContactDetail.telecom [
       fhir:index 0;
       fhir:ContactPoint.system [ fhir:value "url" ];
       fhir:ContactPoint.value [ fhir:value "https://github.com/nih-ncpi" ]     ]
  ], [
     fhir:index 1;
     fhir:ContactDetail.name [ fhir:value "Meen Chul Kim" ];
     fhir:ContactDetail.telecom [
       fhir:index 0;
       fhir:ContactPoint.system [ fhir:value "email" ];
       fhir:ContactPoint.value [ fhir:value "meenchul@d3b.center" ];
       fhir:ContactPoint.use [ fhir:value "work" ]     ]
  ]; # 
  fhir:CodeSystem.description [ fhir:value "The Human Phenotype Ontology (HPO) provides a standardized vocabulary of phenotypic abnormalities encountered in human disease. Please see license of HPO at http://www.human-phenotype-ontology.org"]; # 
  fhir:CodeSystem.valueSet [
     fhir:value "http://fhir.ncpi-project-forge.io/ValueSet/phenotype-codes";
     fhir:link <http://fhir.ncpi-project-forge.io/ValueSet/phenotype-codes>
  ]; # 
  fhir:CodeSystem.hierarchyMeaning [ fhir:value "is-a"]; # 
  fhir:CodeSystem.compositional [ fhir:value "false"^^xsd:boolean]; # 
  fhir:CodeSystem.versionNeeded [ fhir:value "false"^^xsd:boolean]; # 
  fhir:CodeSystem.content [ fhir:value "fragment"]; # 
  fhir:CodeSystem.count [ fhir:value "1880"^^xsd:nonNegativeInteger]; # 
  fhir:CodeSystem.filter [
     fhir:index 0;
     fhir:CodeSystem.filter.code [ fhir:value "root" ];
     fhir:CodeSystem.filter.operator [
       fhir:value "=";
       fhir:index 0     ];
     fhir:CodeSystem.filter.value [ fhir:value "True or false." ]
  ], [
     fhir:index 1;
     fhir:CodeSystem.filter.code [ fhir:value "deprecated" ];
     fhir:CodeSystem.filter.operator [
       fhir:value "=";
       fhir:index 0     ];
     fhir:CodeSystem.filter.value [ fhir:value "True or false." ]
  ], [
     fhir:index 2;
     fhir:CodeSystem.filter.code [ fhir:value "imported" ];
     fhir:CodeSystem.filter.operator [
       fhir:value "=";
       fhir:index 0     ];
     fhir:CodeSystem.filter.value [ fhir:value "True or false" ]
  ]; # 
  fhir:CodeSystem.property [
     fhir:index 0;
     fhir:CodeSystem.property.code [ fhir:value "parent" ];
     fhir:CodeSystem.property.description [ fhir:value "Parent codes." ];
     fhir:CodeSystem.property.type [ fhir:value "code" ]
  ], [
     fhir:index 1;
     fhir:CodeSystem.property.code [ fhir:value "imported" ];
     fhir:CodeSystem.property.description [ fhir:value "Indicates if the concept is imported from another code system." ];
     fhir:CodeSystem.property.type [ fhir:value "boolean" ]
  ], [
     fhir:index 2;
     fhir:CodeSystem.property.code [ fhir:value "root" ];
     fhir:CodeSystem.property.description [ fhir:value "Indicates if this concept is a root concept (i.e. Thing is equivalent or a direct parent)" ];
     fhir:CodeSystem.property.type [ fhir:value "boolean" ]
  ], [
     fhir:index 3;
     fhir:CodeSystem.property.code [ fhir:value "deprecated" ];
     fhir:CodeSystem.property.description [ fhir:value "Indicates if this concept is deprecated." ];
     fhir:CodeSystem.property.type [ fhir:value "boolean" ]
  ]; # 
  fhir:CodeSystem.concept [
     fhir:index 0;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000365" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hearing impairment" ]
  ], [
     fhir:index 1;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002564" ];
     fhir:CodeSystem.concept.display [ fhir:value "obsolete Malformation of the heart and great vessels" ]
  ], [
     fhir:index 2;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001028" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hemangioma" ]
  ], [
     fhir:index 3;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000476" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cystic hygroma" ]
  ], [
     fhir:index 4;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000568" ];
     fhir:CodeSystem.concept.display [ fhir:value "Microphthalmia" ]
  ], [
     fhir:index 5;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000518" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cataract" ]
  ], [
     fhir:index 6;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000612" ];
     fhir:CodeSystem.concept.display [ fhir:value "Iris coloboma" ]
  ], [
     fhir:index 7;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000567" ];
     fhir:CodeSystem.concept.display [ fhir:value "Chorioretinal coloboma" ]
  ], [
     fhir:index 8;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000316" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypertelorism" ]
  ], [
     fhir:index 9;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000482" ];
     fhir:CodeSystem.concept.display [ fhir:value "Microcornea" ]
  ], [
     fhir:index 10;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000588" ];
     fhir:CodeSystem.concept.display [ fhir:value "Optic nerve coloboma" ]
  ], [
     fhir:index 11;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004426" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the cheek" ]
  ], [
     fhir:index 12;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009125" ];
     fhir:CodeSystem.concept.display [ fhir:value "Lipodystrophy" ]
  ], [
     fhir:index 13;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002023" ];
     fhir:CodeSystem.concept.display [ fhir:value "Anal atresia" ]
  ], [
     fhir:index 14;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003468" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal vertebral morphology" ]
  ], [
     fhir:index 15;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000545" ];
     fhir:CodeSystem.concept.display [ fhir:value "Myopia" ]
  ], [
     fhir:index 16;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000122" ];
     fhir:CodeSystem.concept.display [ fhir:value "Unilateral renal agenesis" ]
  ], [
     fhir:index 17;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002143" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the spinal cord" ]
  ], [
     fhir:index 18;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003508" ];
     fhir:CodeSystem.concept.display [ fhir:value "Proportionate short stature" ]
  ], [
     fhir:index 19;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000271" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the face" ]
  ], [
     fhir:index 20;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000637" ];
     fhir:CodeSystem.concept.display [ fhir:value "Long palpebral fissure" ]
  ], [
     fhir:index 21;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000492" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal eyelid morphology" ]
  ], [
     fhir:index 22;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000389" ];
     fhir:CodeSystem.concept.display [ fhir:value "Chronic otitis media" ]
  ], [
     fhir:index 23;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000400" ];
     fhir:CodeSystem.concept.display [ fhir:value "Macrotia" ]
  ], [
     fhir:index 24;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000405" ];
     fhir:CodeSystem.concept.display [ fhir:value "Conductive hearing impairment" ]
  ], [
     fhir:index 25;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012712" ];
     fhir:CodeSystem.concept.display [ fhir:value "Mild hearing impairment" ]
  ], [
     fhir:index 26;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005280" ];
     fhir:CodeSystem.concept.display [ fhir:value "Depressed nasal bridge" ]
  ], [
     fhir:index 27;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000431" ];
     fhir:CodeSystem.concept.display [ fhir:value "Wide nasal bridge" ]
  ], [
     fhir:index 28;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000319" ];
     fhir:CodeSystem.concept.display [ fhir:value "Smooth philtrum" ]
  ], [
     fhir:index 29;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000175" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cleft palate" ]
  ], [
     fhir:index 30;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001611" ];
     fhir:CodeSystem.concept.display [ fhir:value "Nasal speech" ]
  ], [
     fhir:index 31;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002099" ];
     fhir:CodeSystem.concept.display [ fhir:value "Asthma" ]
  ], [
     fhir:index 32;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001397" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hepatic steatosis" ]
  ], [
     fhir:index 33;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001081" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cholelithiasis" ]
  ], [
     fhir:index 34;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002650" ];
     fhir:CodeSystem.concept.display [ fhir:value "Scoliosis" ]
  ], [
     fhir:index 35;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001212" ];
     fhir:CodeSystem.concept.display [ fhir:value "Prominent fingertip pads" ]
  ], [
     fhir:index 36;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001328" ];
     fhir:CodeSystem.concept.display [ fhir:value "Specific learning disability" ]
  ], [
     fhir:index 37;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000824" ];
     fhir:CodeSystem.concept.display [ fhir:value "Growth hormone deficiency" ]
  ], [
     fhir:index 38;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002607" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bowel incontinence" ]
  ], [
     fhir:index 39;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100731" ];
     fhir:CodeSystem.concept.display [ fhir:value "Transverse facial cleft" ]
  ], [
     fhir:index 40;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000528" ];
     fhir:CodeSystem.concept.display [ fhir:value "Anophthalmia" ]
  ], [
     fhir:index 41;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000601" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypotelorism" ]
  ], [
     fhir:index 42;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000369" ];
     fhir:CodeSystem.concept.display [ fhir:value "Low-set ears" ]
  ], [
     fhir:index 43;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001274" ];
     fhir:CodeSystem.concept.display [ fhir:value "Agenesis of corpus callosum" ]
  ], [
     fhir:index 44;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002084" ];
     fhir:CodeSystem.concept.display [ fhir:value "Encephalocele" ]
  ], [
     fhir:index 45;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007033" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cerebellar dysplasia" ]
  ], [
     fhir:index 46;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100336" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bilateral cleft lip" ]
  ], [
     fhir:index 47;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100337" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bilateral cleft palate" ]
  ], [
     fhir:index 48;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001511" ];
     fhir:CodeSystem.concept.display [ fhir:value "Intrauterine growth retardation" ]
  ], [
     fhir:index 49;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011451" ];
     fhir:CodeSystem.concept.display [ fhir:value "Congenital microcephaly" ]
  ], [
     fhir:index 50;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000324" ];
     fhir:CodeSystem.concept.display [ fhir:value "Facial asymmetry" ]
  ], [
     fhir:index 51;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000581" ];
     fhir:CodeSystem.concept.display [ fhir:value "Blepharophimosis" ]
  ], [
     fhir:index 52;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000508" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ptosis" ]
  ], [
     fhir:index 53;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008551" ];
     fhir:CodeSystem.concept.display [ fhir:value "Microtia" ]
  ], [
     fhir:index 54;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001631" ];
     fhir:CodeSystem.concept.display [ fhir:value "Atrial septal defect" ]
  ], [
     fhir:index 55;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000085" ];
     fhir:CodeSystem.concept.display [ fhir:value "Horseshoe kidney" ]
  ], [
     fhir:index 56;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011927" ];
     fhir:CodeSystem.concept.display [ fhir:value "Short digit" ]
  ], [
     fhir:index 57;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001156" ];
     fhir:CodeSystem.concept.display [ fhir:value "Brachydactyly" ]
  ], [
     fhir:index 58;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002066" ];
     fhir:CodeSystem.concept.display [ fhir:value "Gait ataxia" ]
  ], [
     fhir:index 59;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001250" ];
     fhir:CodeSystem.concept.display [ fhir:value "Seizure" ]
  ], [
     fhir:index 60;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001263" ];
     fhir:CodeSystem.concept.display [ fhir:value "Global developmental delay" ]
  ], [
     fhir:index 61;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001562" ];
     fhir:CodeSystem.concept.display [ fhir:value "Oligohydramnios" ]
  ], [
     fhir:index 62;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001195" ];
     fhir:CodeSystem.concept.display [ fhir:value "Single umbilical artery" ]
  ], [
     fhir:index 63;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006349" ];
     fhir:CodeSystem.concept.display [ fhir:value "Agenesis of permanent teeth" ]
  ], [
     fhir:index 64;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000668" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypodontia" ]
  ], [
     fhir:index 65;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000677" ];
     fhir:CodeSystem.concept.display [ fhir:value "Oligodontia" ]
  ], [
     fhir:index 66;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001252" ];
     fhir:CodeSystem.concept.display [ fhir:value "Muscular hypotonia" ]
  ], [
     fhir:index 67;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003429" ];
     fhir:CodeSystem.concept.display [ fhir:value "CNS hypomyelination" ]
  ], [
     fhir:index 68;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010864" ];
     fhir:CodeSystem.concept.display [ fhir:value "Intellectual disability, severe" ]
  ], [
     fhir:index 69;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004325" ];
     fhir:CodeSystem.concept.display [ fhir:value "Decreased body weight" ]
  ], [
     fhir:index 70;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000666" ];
     fhir:CodeSystem.concept.display [ fhir:value "Horizontal nystagmus" ]
  ], [
     fhir:index 71;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000218" ];
     fhir:CodeSystem.concept.display [ fhir:value "High palate" ]
  ], [
     fhir:index 72;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010809" ];
     fhir:CodeSystem.concept.display [ fhir:value "Broad uvula" ]
  ], [
     fhir:index 73;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000767" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pectus excavatum" ]
  ], [
     fhir:index 74;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003691" ];
     fhir:CodeSystem.concept.display [ fhir:value "Scapular winging" ]
  ], [
     fhir:index 75;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002616" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aortic root aneurysm" ]
  ], [
     fhir:index 76;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001601" ];
     fhir:CodeSystem.concept.display [ fhir:value "Laryngomalacia" ]
  ], [
     fhir:index 77;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002021" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pyloric stenosis" ]
  ], [
     fhir:index 78;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001388" ];
     fhir:CodeSystem.concept.display [ fhir:value "Joint laxity" ]
  ], [
     fhir:index 79;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001187" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyperextensibility of the finger joints" ]
  ], [
     fhir:index 80;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000741" ];
     fhir:CodeSystem.concept.display [ fhir:value "Apathy" ]
  ], [
     fhir:index 81;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000817" ];
     fhir:CodeSystem.concept.display [ fhir:value "Poor eye contact" ]
  ], [
     fhir:index 82;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000821" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypothyroidism" ]
  ], [
     fhir:index 83;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000002" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of body height" ]
  ], [
     fhir:index 84;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000079" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the urinary system" ]
  ], [
     fhir:index 85;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000164" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the dentition" ]
  ], [
     fhir:index 86;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000364" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hearing abnormality" ]
  ], [
     fhir:index 87;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000366" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the nose" ]
  ], [
     fhir:index 88;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000464" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the neck" ]
  ], [
     fhir:index 89;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000707" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the nervous system" ]
  ], [
     fhir:index 90;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000708" ];
     fhir:CodeSystem.concept.display [ fhir:value "Behavioral abnormality" ]
  ], [
     fhir:index 91;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000769" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the breast" ]
  ], [
     fhir:index 92;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000772" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the ribs" ]
  ], [
     fhir:index 93;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000775" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the diaphragm" ]
  ], [
     fhir:index 94;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000889" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the clavicle" ]
  ], [
     fhir:index 95;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000925" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the vertebral column" ]
  ], [
     fhir:index 96;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001080" ];
     fhir:CodeSystem.concept.display [ fhir:value "Biliary tract abnormality" ]
  ], [
     fhir:index 97;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001392" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the liver" ]
  ], [
     fhir:index 98;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001438" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal abdomen morphology" ]
  ], [
     fhir:index 99;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001608" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the voice" ]
  ], [
     fhir:index 100;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001627" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal heart morphology" ]
  ], [
     fhir:index 101;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001732" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the pancreas" ]
  ], [
     fhir:index 102;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001739" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the nasopharynx" ]
  ], [
     fhir:index 103;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001743" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the spleen" ]
  ], [
     fhir:index 104;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001760" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal foot morphology" ]
  ], [
     fhir:index 105;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001871" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of blood and blood-forming tissues" ]
  ], [
     fhir:index 106;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002031" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal esophagus morphology" ]
  ], [
     fhir:index 107;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002244" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the small intestine" ]
  ], [
     fhir:index 108;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002246" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the duodenum" ]
  ], [
     fhir:index 109;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002250" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal large intestine morphology" ]
  ], [
     fhir:index 110;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002644" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of pelvic girdle bone morphology" ]
  ], [
     fhir:index 111;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002664" ];
     fhir:CodeSystem.concept.display [ fhir:value "Neoplasm" ]
  ], [
     fhir:index 112;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002715" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the immune system" ]
  ], [
     fhir:index 113;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002814" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the lower limb" ]
  ], [
     fhir:index 114;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002817" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the upper limb" ]
  ], [
     fhir:index 115;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005483" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal epiglottis morphology" ]
  ], [
     fhir:index 116;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008777" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal vocal cord morphology" ]
  ], [
     fhir:index 117;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011844" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal appendicular skeleton morphology" ]
  ], [
     fhir:index 118;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012732" ];
     fhir:CodeSystem.concept.display [ fhir:value "Anorectal anomaly" ]
  ], [
     fhir:index 119;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001508" ];
     fhir:CodeSystem.concept.display [ fhir:value "Failure to thrive" ]
  ], [
     fhir:index 120;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002902" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyponatremia" ]
  ], [
     fhir:index 121;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012236" ];
     fhir:CodeSystem.concept.display [ fhir:value "Elevated sweat chloride" ]
  ], [
     fhir:index 122;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000347" ];
     fhir:CodeSystem.concept.display [ fhir:value "Micrognathia" ]
  ], [
     fhir:index 123;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000926" ];
     fhir:CodeSystem.concept.display [ fhir:value "Platyspondyly" ]
  ], [
     fhir:index 124;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001371" ];
     fhir:CodeSystem.concept.display [ fhir:value "Flexion contracture" ]
  ], [
     fhir:index 125;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001875" ];
     fhir:CodeSystem.concept.display [ fhir:value "Neutropenia" ]
  ], [
     fhir:index 126;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001888" ];
     fhir:CodeSystem.concept.display [ fhir:value "Lymphopenia" ]
  ], [
     fhir:index 127;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002857" ];
     fhir:CodeSystem.concept.display [ fhir:value "Genu valgum" ]
  ], [
     fhir:index 128;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002986" ];
     fhir:CodeSystem.concept.display [ fhir:value "Radial bowing" ]
  ], [
     fhir:index 129;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003015" ];
     fhir:CodeSystem.concept.display [ fhir:value "Flared metaphysis" ]
  ], [
     fhir:index 130;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003025" ];
     fhir:CodeSystem.concept.display [ fhir:value "Metaphyseal irregularity" ]
  ], [
     fhir:index 131;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003097" ];
     fhir:CodeSystem.concept.display [ fhir:value "Short femur" ]
  ], [
     fhir:index 132;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003300" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ovoid vertebral bodies" ]
  ], [
     fhir:index 133;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003307" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyperlordosis" ]
  ], [
     fhir:index 134;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004209" ];
     fhir:CodeSystem.concept.display [ fhir:value "Clinodactyly of the 5th finger" ]
  ], [
     fhir:index 135;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004322" ];
     fhir:CodeSystem.concept.display [ fhir:value "Short stature" ]
  ], [
     fhir:index 136;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005792" ];
     fhir:CodeSystem.concept.display [ fhir:value "Short humerus" ]
  ], [
     fhir:index 137;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006248" ];
     fhir:CodeSystem.concept.display [ fhir:value "Limited wrist movement" ]
  ], [
     fhir:index 138;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000944" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the metaphysis" ]
  ], [
     fhir:index 139;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011921" ];
     fhir:CodeSystem.concept.display [ fhir:value "Exudative pleural effusion" ]
  ], [
     fhir:index 140;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003043" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the shoulder" ]
  ], [
     fhir:index 141;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000290" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the forehead" ]
  ], [
     fhir:index 142;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005288" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the nares" ]
  ], [
     fhir:index 143;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000234" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the head" ]
  ], [
     fhir:index 144;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004323" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of body weight" ]
  ], [
     fhir:index 145;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000483" ];
     fhir:CodeSystem.concept.display [ fhir:value "Astigmatism" ]
  ], [
     fhir:index 146;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011003" ];
     fhir:CodeSystem.concept.display [ fhir:value "High myopia" ]
  ], [
     fhir:index 147;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000470" ];
     fhir:CodeSystem.concept.display [ fhir:value "Short neck" ]
  ], [
     fhir:index 148;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030044" ];
     fhir:CodeSystem.concept.display [ fhir:value "Flexion contracture of digit" ]
  ], [
     fhir:index 149;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100871" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the palm" ]
  ], [
     fhir:index 150;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004334" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dermal atrophy" ]
  ], [
     fhir:index 151;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001845" ];
     fhir:CodeSystem.concept.display [ fhir:value "Overlapping toe" ]
  ], [
     fhir:index 152;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000496" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of eye movement" ]
  ], [
     fhir:index 153;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001780" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of toe" ]
  ], [
     fhir:index 154;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001626" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the cardiovascular system" ]
  ], [
     fhir:index 155;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002086" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the respiratory system" ]
  ], [
     fhir:index 156;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000818" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the endocrine system" ]
  ], [
     fhir:index 157;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012372" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal eye morphology" ]
  ], [
     fhir:index 158;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009473" ];
     fhir:CodeSystem.concept.display [ fhir:value "Joint contracture of the hand" ]
  ], [
     fhir:index 159;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003199" ];
     fhir:CodeSystem.concept.display [ fhir:value "Decreased muscle mass" ]
  ], [
     fhir:index 160;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003202" ];
     fhir:CodeSystem.concept.display [ fhir:value "Skeletal muscle atrophy" ]
  ], [
     fhir:index 161;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003551" ];
     fhir:CodeSystem.concept.display [ fhir:value "Difficulty climbing stairs" ]
  ], [
     fhir:index 162;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002355" ];
     fhir:CodeSystem.concept.display [ fhir:value "Difficulty walking" ]
  ], [
     fhir:index 163;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003546" ];
     fhir:CodeSystem.concept.display [ fhir:value "Exercise intolerance" ]
  ], [
     fhir:index 164;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003325" ];
     fhir:CodeSystem.concept.display [ fhir:value "Limb-girdle muscle weakness" ]
  ], [
     fhir:index 165;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003701" ];
     fhir:CodeSystem.concept.display [ fhir:value "Proximal muscle weakness" ]
  ], [
     fhir:index 166;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003547" ];
     fhir:CodeSystem.concept.display [ fhir:value "Shoulder girdle muscle weakness" ]
  ], [
     fhir:index 167;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007340" ];
     fhir:CodeSystem.concept.display [ fhir:value "Lower limb muscle weakness" ]
  ], [
     fhir:index 168;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002168" ];
     fhir:CodeSystem.concept.display [ fhir:value "Scanning speech" ]
  ], [
     fhir:index 169;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001265" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyporeflexia" ]
  ], [
     fhir:index 170;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001284" ];
     fhir:CodeSystem.concept.display [ fhir:value "Areflexia" ]
  ], [
     fhir:index 171;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003477" ];
     fhir:CodeSystem.concept.display [ fhir:value "Peripheral axonal neuropathy" ]
  ], [
     fhir:index 172;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000924" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the skeletal system" ]
  ], [
     fhir:index 173;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001291" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal cranial nerve morphology" ]
  ], [
     fhir:index 174;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003687" ];
     fhir:CodeSystem.concept.display [ fhir:value "Centrally nucleated skeletal muscle fibers" ]
  ], [
     fhir:index 175;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001324" ];
     fhir:CodeSystem.concept.display [ fhir:value "Muscle weakness" ]
  ], [
     fhir:index 176;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002515" ];
     fhir:CodeSystem.concept.display [ fhir:value "Waddling gait" ]
  ], [
     fhir:index 177;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100280" ];
     fhir:CodeSystem.concept.display [ fhir:value "Crohn's disease" ]
  ], [
     fhir:index 178;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002631" ];
     fhir:CodeSystem.concept.display [ fhir:value "obsolete Dilatation of ascending aorta" ]
  ], [
     fhir:index 179;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100026" ];
     fhir:CodeSystem.concept.display [ fhir:value "Arteriovenous malformation" ]
  ], [
     fhir:index 180;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002637" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cerebral ischemia" ]
  ], [
     fhir:index 181;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002619" ];
     fhir:CodeSystem.concept.display [ fhir:value "Varicose veins" ]
  ], [
     fhir:index 182;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001159" ];
     fhir:CodeSystem.concept.display [ fhir:value "Syndactyly" ]
  ], [
     fhir:index 183;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002069" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bilateral tonic-clonic seizure" ]
  ], [
     fhir:index 184;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000977" ];
     fhir:CodeSystem.concept.display [ fhir:value "Soft skin" ]
  ], [
     fhir:index 185;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010648" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dermal translucency" ]
  ], [
     fhir:index 186;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000978" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bruising susceptibility" ]
  ], [
     fhir:index 187;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001956" ];
     fhir:CodeSystem.concept.display [ fhir:value "Truncal obesity" ]
  ], [
     fhir:index 188;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000189" ];
     fhir:CodeSystem.concept.display [ fhir:value "Narrow palate" ]
  ], [
     fhir:index 189;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000678" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dental crowding" ]
  ], [
     fhir:index 190;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002870" ];
     fhir:CodeSystem.concept.display [ fhir:value "Obstructive sleep apnea" ]
  ], [
     fhir:index 191;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001763" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pes planus" ]
  ], [
     fhir:index 192;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000782" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the scapula" ]
  ], [
     fhir:index 193;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001600" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the larynx" ]
  ], [
     fhir:index 194;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002088" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal lung morphology" ]
  ], [
     fhir:index 195;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011407" ];
     fhir:CodeSystem.concept.display [ fhir:value "Proportionate tall stature" ]
  ], [
     fhir:index 196;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000541" ];
     fhir:CodeSystem.concept.display [ fhir:value "Retinal detachment" ]
  ], [
     fhir:index 197;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001373" ];
     fhir:CodeSystem.concept.display [ fhir:value "Joint dislocation" ]
  ], [
     fhir:index 198;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000938" ];
     fhir:CodeSystem.concept.display [ fhir:value "Osteopenia" ]
  ], [
     fhir:index 199;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002942" ];
     fhir:CodeSystem.concept.display [ fhir:value "Thoracic kyphosis" ]
  ], [
     fhir:index 200;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001840" ];
     fhir:CodeSystem.concept.display [ fhir:value "Metatarsus adductus" ]
  ], [
     fhir:index 201;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001844" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the hallux" ]
  ], [
     fhir:index 202;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001765" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hammertoe" ]
  ], [
     fhir:index 203;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000606" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the periorbital region" ]
  ], [
     fhir:index 204;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002757" ];
     fhir:CodeSystem.concept.display [ fhir:value "Recurrent fractures" ]
  ], [
     fhir:index 205;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000647" ];
     fhir:CodeSystem.concept.display [ fhir:value "Sclerocornea" ]
  ], [
     fhir:index 206;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001166" ];
     fhir:CodeSystem.concept.display [ fhir:value "Arachnodactyly" ]
  ], [
     fhir:index 207;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005490" ];
     fhir:CodeSystem.concept.display [ fhir:value "Postnatal macrocephaly" ]
  ], [
     fhir:index 208;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011363" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of hair growth rate" ]
  ], [
     fhir:index 209;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000276" ];
     fhir:CodeSystem.concept.display [ fhir:value "Long face" ]
  ], [
     fhir:index 210;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000275" ];
     fhir:CodeSystem.concept.display [ fhir:value "Narrow face" ]
  ], [
     fhir:index 211;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000337" ];
     fhir:CodeSystem.concept.display [ fhir:value "Broad forehead" ]
  ], [
     fhir:index 212;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002267" ];
     fhir:CodeSystem.concept.display [ fhir:value "Exaggerated startle response" ]
  ], [
     fhir:index 213;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002187" ];
     fhir:CodeSystem.concept.display [ fhir:value "Intellectual disability, profound" ]
  ], [
     fhir:index 214;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000728" ];
     fhir:CodeSystem.concept.display [ fhir:value "Impaired ability to form peer relationships" ]
  ], [
     fhir:index 215;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000733" ];
     fhir:CodeSystem.concept.display [ fhir:value "Stereotypy" ]
  ], [
     fhir:index 216;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000739" ];
     fhir:CodeSystem.concept.display [ fhir:value "Anxiety" ]
  ], [
     fhir:index 217;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000929" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal skull morphology" ]
  ], [
     fhir:index 218;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001965" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal scalp morphology" ]
  ], [
     fhir:index 219;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100538" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the supraorbital ridges" ]
  ], [
     fhir:index 220;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000309" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the midface" ]
  ], [
     fhir:index 221;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000277" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the mandible" ]
  ], [
     fhir:index 222;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000765" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the thorax" ]
  ], [
     fhir:index 223;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100008" ];
     fhir:CodeSystem.concept.display [ fhir:value "Schwannoma" ]
  ], [
     fhir:index 224;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030038" ];
     fhir:CodeSystem.concept.display [ fhir:value "Enchondroma" ]
  ], [
     fhir:index 225;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100777" ];
     fhir:CodeSystem.concept.display [ fhir:value "Exostoses" ]
  ], [
     fhir:index 226;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011663" ];
     fhir:CodeSystem.concept.display [ fhir:value "Right ventricular cardiomyopathy" ]
  ], [
     fhir:index 227;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011675" ];
     fhir:CodeSystem.concept.display [ fhir:value "Arrhythmia" ]
  ], [
     fhir:index 228;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001962" ];
     fhir:CodeSystem.concept.display [ fhir:value "Palpitations" ]
  ], [
     fhir:index 229;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001279" ];
     fhir:CodeSystem.concept.display [ fhir:value "Syncope" ]
  ], [
     fhir:index 230;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004756" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ventricular tachycardia" ]
  ], [
     fhir:index 231;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000252" ];
     fhir:CodeSystem.concept.display [ fhir:value "Microcephaly" ]
  ], [
     fhir:index 232;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000303" ];
     fhir:CodeSystem.concept.display [ fhir:value "Mandibular prognathia" ]
  ], [
     fhir:index 233;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000664" ];
     fhir:CodeSystem.concept.display [ fhir:value "Synophrys" ]
  ], [
     fhir:index 234;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001609" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hoarse voice" ]
  ], [
     fhir:index 235;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002558" ];
     fhir:CodeSystem.concept.display [ fhir:value "Supernumerary nipple" ]
  ], [
     fhir:index 236;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001634" ];
     fhir:CodeSystem.concept.display [ fhir:value "Mitral valve prolapse" ]
  ], [
     fhir:index 237;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000028" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cryptorchidism" ]
  ], [
     fhir:index 238;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000973" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cutis laxa" ]
  ], [
     fhir:index 239;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001518" ];
     fhir:CodeSystem.concept.display [ fhir:value "Small for gestational age" ]
  ], [
     fhir:index 240;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000527" ];
     fhir:CodeSystem.concept.display [ fhir:value "Long eyelashes" ]
  ], [
     fhir:index 241;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002808" ];
     fhir:CodeSystem.concept.display [ fhir:value "Kyphosis" ]
  ], [
     fhir:index 242;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000248" ];
     fhir:CodeSystem.concept.display [ fhir:value "Brachycephaly" ]
  ], [
     fhir:index 243;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000505" ];
     fhir:CodeSystem.concept.display [ fhir:value "Visual impairment" ]
  ], [
     fhir:index 244;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000512" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal electroretinogram" ]
  ], [
     fhir:index 245;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000517" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the lens" ]
  ], [
     fhir:index 246;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000529" ];
     fhir:CodeSystem.concept.display [ fhir:value "Progressive visual loss" ]
  ], [
     fhir:index 247;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000586" ];
     fhir:CodeSystem.concept.display [ fhir:value "Shallow orbits" ]
  ], [
     fhir:index 248;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000603" ];
     fhir:CodeSystem.concept.display [ fhir:value "Central scotoma" ]
  ], [
     fhir:index 249;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000939" ];
     fhir:CodeSystem.concept.display [ fhir:value "Osteoporosis" ]
  ], [
     fhir:index 250;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001377" ];
     fhir:CodeSystem.concept.display [ fhir:value "Limited elbow extension" ]
  ], [
     fhir:index 251;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001387" ];
     fhir:CodeSystem.concept.display [ fhir:value "Joint stiffness" ]
  ], [
     fhir:index 252;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001822" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hallux valgus" ]
  ], [
     fhir:index 253;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002657" ];
     fhir:CodeSystem.concept.display [ fhir:value "Spondylometaphyseal dysplasia" ]
  ], [
     fhir:index 254;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003026" ];
     fhir:CodeSystem.concept.display [ fhir:value "Short long bone" ]
  ], [
     fhir:index 255;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006462" ];
     fhir:CodeSystem.concept.display [ fhir:value "Generalized bone demineralization" ]
  ], [
     fhir:index 256;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008873" ];
     fhir:CodeSystem.concept.display [ fhir:value "Disproportionate short-limb short stature" ]
  ], [
     fhir:index 257;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008905" ];
     fhir:CodeSystem.concept.display [ fhir:value "Rhizomelia" ]
  ], [
     fhir:index 258;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008922" ];
     fhir:CodeSystem.concept.display [ fhir:value "Childhood-onset short-trunk short stature" ]
  ], [
     fhir:index 259;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0200020" ];
     fhir:CodeSystem.concept.display [ fhir:value "Corneal erosion" ]
  ], [
     fhir:index 260;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001172" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal thumb morphology" ]
  ], [
     fhir:index 261;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002286" ];
     fhir:CodeSystem.concept.display [ fhir:value "Fair hair" ]
  ], [
     fhir:index 262;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010719" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of hair texture" ]
  ], [
     fhir:index 263;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010720" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal hair pattern" ]
  ], [
     fhir:index 264;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001635" ];
     fhir:CodeSystem.concept.display [ fhir:value "Congestive heart failure" ]
  ], [
     fhir:index 265;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001644" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dilated cardiomyopathy" ]
  ], [
     fhir:index 266;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001663" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ventricular fibrillation" ]
  ], [
     fhir:index 267;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011712" ];
     fhir:CodeSystem.concept.display [ fhir:value "Right bundle branch block" ]
  ], [
     fhir:index 268;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000272" ];
     fhir:CodeSystem.concept.display [ fhir:value "Malar flattening" ]
  ], [
     fhir:index 269;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000286" ];
     fhir:CodeSystem.concept.display [ fhir:value "Epicanthus" ]
  ], [
     fhir:index 270;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000322" ];
     fhir:CodeSystem.concept.display [ fhir:value "Short philtrum" ]
  ], [
     fhir:index 271;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000463" ];
     fhir:CodeSystem.concept.display [ fhir:value "Anteverted nares" ]
  ], [
     fhir:index 272;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000494" ];
     fhir:CodeSystem.concept.display [ fhir:value "Downslanted palpebral fissures" ]
  ], [
     fhir:index 273;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000543" ];
     fhir:CodeSystem.concept.display [ fhir:value "Optic disc pallor" ]
  ], [
     fhir:index 274;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000699" ];
     fhir:CodeSystem.concept.display [ fhir:value "Diastema" ]
  ], [
     fhir:index 275;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000773" ];
     fhir:CodeSystem.concept.display [ fhir:value "Short ribs" ]
  ], [
     fhir:index 276;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000887" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cupped ribs" ]
  ], [
     fhir:index 277;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000946" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoplastic ilia" ]
  ], [
     fhir:index 278;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000954" ];
     fhir:CodeSystem.concept.display [ fhir:value "Single transverse palmar crease" ]
  ], [
     fhir:index 279;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001182" ];
     fhir:CodeSystem.concept.display [ fhir:value "Tapered finger" ]
  ], [
     fhir:index 280;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001537" ];
     fhir:CodeSystem.concept.display [ fhir:value "Umbilical hernia" ]
  ], [
     fhir:index 281;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002007" ];
     fhir:CodeSystem.concept.display [ fhir:value "Frontal bossing" ]
  ], [
     fhir:index 282;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002980" ];
     fhir:CodeSystem.concept.display [ fhir:value "Femoral bowing" ]
  ], [
     fhir:index 283;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002982" ];
     fhir:CodeSystem.concept.display [ fhir:value "Tibial bowing" ]
  ], [
     fhir:index 284;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003021" ];
     fhir:CodeSystem.concept.display [ fhir:value "Metaphyseal cupping" ]
  ], [
     fhir:index 285;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005011" ];
     fhir:CodeSystem.concept.display [ fhir:value "Mesomelic arm shortening" ]
  ], [
     fhir:index 286;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008803" ];
     fhir:CodeSystem.concept.display [ fhir:value "obsolete Narrow sacroiliac notch" ]
  ], [
     fhir:index 287;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009117" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aplasia/Hypoplasia of the maxilla" ]
  ], [
     fhir:index 288;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011220" ];
     fhir:CodeSystem.concept.display [ fhir:value "Prominent forehead" ]
  ], [
     fhir:index 289;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012801" ];
     fhir:CodeSystem.concept.display [ fhir:value "Narrow jaw" ]
  ], [
     fhir:index 290;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000243" ];
     fhir:CodeSystem.concept.display [ fhir:value "Trigonocephaly" ]
  ], [
     fhir:index 291;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000358" ];
     fhir:CodeSystem.concept.display [ fhir:value "Posteriorly rotated ears" ]
  ], [
     fhir:index 292;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000411" ];
     fhir:CodeSystem.concept.display [ fhir:value "Protruding ear" ]
  ], [
     fhir:index 293;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000646" ];
     fhir:CodeSystem.concept.display [ fhir:value "Amblyopia" ]
  ], [
     fhir:index 294;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002812" ];
     fhir:CodeSystem.concept.display [ fhir:value "Coxa vara" ]
  ], [
     fhir:index 295;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002970" ];
     fhir:CodeSystem.concept.display [ fhir:value "Genu varum" ]
  ], [
     fhir:index 296;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012775" ];
     fhir:CodeSystem.concept.display [ fhir:value "Stellate iris" ]
  ], [
     fhir:index 297;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000278" ];
     fhir:CodeSystem.concept.display [ fhir:value "Retrognathia" ]
  ], [
     fhir:index 298;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009796" ];
     fhir:CodeSystem.concept.display [ fhir:value "Branchial cyst" ]
  ], [
     fhir:index 299;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002474" ];
     fhir:CodeSystem.concept.display [ fhir:value "Expressive language delay" ]
  ], [
     fhir:index 300;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007018" ];
     fhir:CodeSystem.concept.display [ fhir:value "Attention deficit hyperactivity disorder" ]
  ], [
     fhir:index 301;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003198" ];
     fhir:CodeSystem.concept.display [ fhir:value "Myopathy" ]
  ], [
     fhir:index 302;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003324" ];
     fhir:CodeSystem.concept.display [ fhir:value "Generalized muscle weakness" ]
  ], [
     fhir:index 303;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003552" ];
     fhir:CodeSystem.concept.display [ fhir:value "Muscle stiffness" ]
  ], [
     fhir:index 304;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003554" ];
     fhir:CodeSystem.concept.display [ fhir:value "Type 2 muscle fiber atrophy" ]
  ], [
     fhir:index 305;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003557" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased variability in muscle fiber diameter" ]
  ], [
     fhir:index 306;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009025" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased connective tissue" ]
  ], [
     fhir:index 307;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003635" ];
     fhir:CodeSystem.concept.display [ fhir:value "Loss of subcutaneous adipose tissue in limbs" ]
  ], [
     fhir:index 308;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002597" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the vasculature" ]
  ], [
     fhir:index 309;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001649" ];
     fhir:CodeSystem.concept.display [ fhir:value "Tachycardia" ]
  ], [
     fhir:index 310;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001638" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cardiomyopathy" ]
  ], [
     fhir:index 311;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001654" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal heart valve morphology" ]
  ], [
     fhir:index 312;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001671" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal cardiac septum morphology" ]
  ], [
     fhir:index 313;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000103" ];
     fhir:CodeSystem.concept.display [ fhir:value "Polyuria" ]
  ], [
     fhir:index 314;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000114" ];
     fhir:CodeSystem.concept.display [ fhir:value "Proximal tubulopathy" ]
  ], [
     fhir:index 315;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001878" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hemolytic anemia" ]
  ], [
     fhir:index 316;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001931" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypochromic anemia" ]
  ], [
     fhir:index 317;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001935" ];
     fhir:CodeSystem.concept.display [ fhir:value "Microcytic anemia" ]
  ], [
     fhir:index 318;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001959" ];
     fhir:CodeSystem.concept.display [ fhir:value "Polydipsia" ]
  ], [
     fhir:index 319;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001994" ];
     fhir:CodeSystem.concept.display [ fhir:value "Renal Fanconi syndrome" ]
  ], [
     fhir:index 320;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002134" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the basal ganglia" ]
  ], [
     fhir:index 321;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002188" ];
     fhir:CodeSystem.concept.display [ fhir:value "Delayed CNS myelination" ]
  ], [
     fhir:index 322;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002908" ];
     fhir:CodeSystem.concept.display [ fhir:value "Conjugated hyperbilirubinemia" ]
  ], [
     fhir:index 323;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003774" ];
     fhir:CodeSystem.concept.display [ fhir:value "Stage 5 chronic kidney disease" ]
  ], [
     fhir:index 324;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010700" ];
     fhir:CodeSystem.concept.display [ fhir:value "obsolete Total cataract" ]
  ], [
     fhir:index 325;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000193" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bifid uvula" ]
  ], [
     fhir:index 326;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000219" ];
     fhir:CodeSystem.concept.display [ fhir:value "Thin upper lip vermilion" ]
  ], [
     fhir:index 327;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000426" ];
     fhir:CodeSystem.concept.display [ fhir:value "Prominent nasal bridge" ]
  ], [
     fhir:index 328;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000452" ];
     fhir:CodeSystem.concept.display [ fhir:value "Choanal stenosis" ]
  ], [
     fhir:index 329;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000490" ];
     fhir:CodeSystem.concept.display [ fhir:value "Deeply set eye" ]
  ], [
     fhir:index 330;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000540" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypermetropia" ]
  ], [
     fhir:index 331;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000579" ];
     fhir:CodeSystem.concept.display [ fhir:value "Nasolacrimal duct obstruction" ]
  ], [
     fhir:index 332;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000684" ];
     fhir:CodeSystem.concept.display [ fhir:value "Delayed eruption of teeth" ]
  ], [
     fhir:index 333;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000960" ];
     fhir:CodeSystem.concept.display [ fhir:value "Sacral dimple" ]
  ], [
     fhir:index 334;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000998" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypertrichosis" ]
  ], [
     fhir:index 335;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001643" ];
     fhir:CodeSystem.concept.display [ fhir:value "Patent ductus arteriosus" ]
  ], [
     fhir:index 336;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010813" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal number of hair whorls" ]
  ], [
     fhir:index 337;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012384" ];
     fhir:CodeSystem.concept.display [ fhir:value "Rhinitis" ]
  ], [
     fhir:index 338;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012745" ];
     fhir:CodeSystem.concept.display [ fhir:value "Short palpebral fissure" ]
  ], [
     fhir:index 339;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000359" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the inner ear" ]
  ], [
     fhir:index 340;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000429" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the nasal alae" ]
  ], [
     fhir:index 341;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000436" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the nasal tip" ]
  ], [
     fhir:index 342;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000499" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal eyelash morphology" ]
  ], [
     fhir:index 343;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000534" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal eyebrow morphology" ]
  ], [
     fhir:index 344;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000951" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the skin" ]
  ], [
     fhir:index 345;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001000" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of skin pigmentation" ]
  ], [
     fhir:index 346;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001597" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the nail" ]
  ], [
     fhir:index 347;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006483" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal number of teeth" ]
  ], [
     fhir:index 348;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009929" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the columella" ]
  ], [
     fhir:index 349;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011119" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the nasal dorsum" ]
  ], [
     fhir:index 350;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012808" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal nasal base" ]
  ], [
     fhir:index 351;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100490" ];
     fhir:CodeSystem.concept.display [ fhir:value "Camptodactyly of finger" ]
  ], [
     fhir:index 352;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000964" ];
     fhir:CodeSystem.concept.display [ fhir:value "Eczema" ]
  ], [
     fhir:index 353;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004442" ];
     fhir:CodeSystem.concept.display [ fhir:value "Sagittal craniosynostosis" ]
  ], [
     fhir:index 354;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000414" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bulbous nose" ]
  ], [
     fhir:index 355;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003180" ];
     fhir:CodeSystem.concept.display [ fhir:value "Flat acetabular roof" ]
  ], [
     fhir:index 356;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000422" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the nasal bridge" ]
  ], [
     fhir:index 357;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000614" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal nasolacrimal system morphology" ]
  ], [
     fhir:index 358;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001167" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of finger" ]
  ], [
     fhir:index 359;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001595" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal hair morphology" ]
  ], [
     fhir:index 360;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012373" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal eye physiology" ]
  ], [
     fhir:index 361;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001655" ];
     fhir:CodeSystem.concept.display [ fhir:value "Patent foramen ovale" ]
  ], [
     fhir:index 362;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001647" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bicuspid aortic valve" ]
  ], [
     fhir:index 363;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000574" ];
     fhir:CodeSystem.concept.display [ fhir:value "Thick eyebrow" ]
  ], [
     fhir:index 364;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001169" ];
     fhir:CodeSystem.concept.display [ fhir:value "Broad palm" ]
  ], [
     fhir:index 365;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006471" ];
     fhir:CodeSystem.concept.display [ fhir:value "Fixed elbow flexion" ]
  ], [
     fhir:index 366;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008689" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bilateral cryptorchidism" ]
  ], [
     fhir:index 367;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011304" ];
     fhir:CodeSystem.concept.display [ fhir:value "Broad thumb" ]
  ], [
     fhir:index 368;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005110" ];
     fhir:CodeSystem.concept.display [ fhir:value "Atrial fibrillation" ]
  ], [
     fhir:index 369;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001633" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal mitral valve morphology" ]
  ], [
     fhir:index 370;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001641" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal pulmonary valve morphology" ]
  ], [
     fhir:index 371;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001702" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal tricuspid valve morphology" ]
  ], [
     fhir:index 372;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000012" ];
     fhir:CodeSystem.concept.display [ fhir:value "Urinary urgency" ]
  ], [
     fhir:index 373;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000020" ];
     fhir:CodeSystem.concept.display [ fhir:value "Urinary incontinence" ]
  ], [
     fhir:index 374;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000131" ];
     fhir:CodeSystem.concept.display [ fhir:value "Uterine leiomyoma" ]
  ], [
     fhir:index 375;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000132" ];
     fhir:CodeSystem.concept.display [ fhir:value "Menorrhagia" ]
  ], [
     fhir:index 376;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000138" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ovarian cyst" ]
  ], [
     fhir:index 377;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000853" ];
     fhir:CodeSystem.concept.display [ fhir:value "Goiter" ]
  ], [
     fhir:index 378;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000953" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyperpigmentation of the skin" ]
  ], [
     fhir:index 379;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001061" ];
     fhir:CodeSystem.concept.display [ fhir:value "Acne" ]
  ], [
     fhir:index 380;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002315" ];
     fhir:CodeSystem.concept.display [ fhir:value "Headache" ]
  ], [
     fhir:index 381;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004324" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased body weight" ]
  ], [
     fhir:index 382;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000069" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the ureter" ]
  ], [
     fhir:index 383;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000077" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the kidney" ]
  ], [
     fhir:index 384;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000759" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal peripheral nervous system morphology" ]
  ], [
     fhir:index 385;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008069" ];
     fhir:CodeSystem.concept.display [ fhir:value "Neoplasm of the skin" ]
  ], [
     fhir:index 386;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011276" ];
     fhir:CodeSystem.concept.display [ fhir:value "Vascular skin abnormality" ]
  ], [
     fhir:index 387;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000705" ];
     fhir:CodeSystem.concept.display [ fhir:value "Amelogenesis imperfecta" ]
  ], [
     fhir:index 388;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001256" ];
     fhir:CodeSystem.concept.display [ fhir:value "Intellectual disability, mild" ]
  ], [
     fhir:index 389;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000325" ];
     fhir:CodeSystem.concept.display [ fhir:value "Triangular face" ]
  ], [
     fhir:index 390;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000160" ];
     fhir:CodeSystem.concept.display [ fhir:value "Narrow mouth" ]
  ], [
     fhir:index 391;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009487" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ulnar deviation of the hand" ]
  ], [
     fhir:index 392;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001249" ];
     fhir:CodeSystem.concept.display [ fhir:value "Intellectual disability" ]
  ], [
     fhir:index 393;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008064" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ichthyosis" ]
  ], [
     fhir:index 394;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000311" ];
     fhir:CodeSystem.concept.display [ fhir:value "Round face" ]
  ], [
     fhir:index 395;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001653" ];
     fhir:CodeSystem.concept.display [ fhir:value "Mitral regurgitation" ]
  ], [
     fhir:index 396;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001771" ];
     fhir:CodeSystem.concept.display [ fhir:value "Achilles tendon contracture" ]
  ], [
     fhir:index 397;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012032" ];
     fhir:CodeSystem.concept.display [ fhir:value "Lipoma" ]
  ], [
     fhir:index 398;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012368" ];
     fhir:CodeSystem.concept.display [ fhir:value "Flat face" ]
  ], [
     fhir:index 399;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030053" ];
     fhir:CodeSystem.concept.display [ fhir:value "Stiff skin" ]
  ], [
     fhir:index 400;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011124" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of epidermal morphology" ]
  ], [
     fhir:index 401;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011097" ];
     fhir:CodeSystem.concept.display [ fhir:value "Epileptic spasm" ]
  ], [
     fhir:index 402;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000407" ];
     fhir:CodeSystem.concept.display [ fhir:value "Sensorineural hearing impairment" ]
  ], [
     fhir:index 403;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000331" ];
     fhir:CodeSystem.concept.display [ fhir:value "Short chin" ]
  ], [
     fhir:index 404;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000340" ];
     fhir:CodeSystem.concept.display [ fhir:value "Sloping forehead" ]
  ], [
     fhir:index 405;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000486" ];
     fhir:CodeSystem.concept.display [ fhir:value "Strabismus" ]
  ], [
     fhir:index 406;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000713" ];
     fhir:CodeSystem.concept.display [ fhir:value "Agitation" ]
  ], [
     fhir:index 407;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000802" ];
     fhir:CodeSystem.concept.display [ fhir:value "Impotence" ]
  ], [
     fhir:index 408;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001272" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cerebellar atrophy" ]
  ], [
     fhir:index 409;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001276" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypertonia" ]
  ], [
     fhir:index 410;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001321" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cerebellar hypoplasia" ]
  ], [
     fhir:index 411;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001322" ];
     fhir:CodeSystem.concept.display [ fhir:value "obsolete Brain very small" ]
  ], [
     fhir:index 412;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002061" ];
     fhir:CodeSystem.concept.display [ fhir:value "Lower limb spasticity" ]
  ], [
     fhir:index 413;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002529" ];
     fhir:CodeSystem.concept.display [ fhir:value "Neuronal loss in central nervous system" ]
  ], [
     fhir:index 414;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002540" ];
     fhir:CodeSystem.concept.display [ fhir:value "Inability to walk" ]
  ], [
     fhir:index 415;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005484" ];
     fhir:CodeSystem.concept.display [ fhir:value "Postnatal microcephaly" ]
  ], [
     fhir:index 416;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012850" ];
     fhir:CodeSystem.concept.display [ fhir:value "Small intestinal dysmotility" ]
  ], [
     fhir:index 417;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000504" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of vision" ]
  ], [
     fhir:index 418;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002118" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the cerebral ventricles" ]
  ], [
     fhir:index 419;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002363" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of brainstem morphology" ]
  ], [
     fhir:index 420;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010651" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal meningeal morphology" ]
  ], [
     fhir:index 421;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100024" ];
     fhir:CodeSystem.concept.display [ fhir:value "Conspicuously happy disposition" ]
  ], [
     fhir:index 422;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002538" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the cerebral cortex" ]
  ], [
     fhir:index 423;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000054" ];
     fhir:CodeSystem.concept.display [ fhir:value "Micropenis" ]
  ], [
     fhir:index 424;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000215" ];
     fhir:CodeSystem.concept.display [ fhir:value "Thick upper lip vermilion" ]
  ], [
     fhir:index 425;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000293" ];
     fhir:CodeSystem.concept.display [ fhir:value "Full cheeks" ]
  ], [
     fhir:index 426;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000349" ];
     fhir:CodeSystem.concept.display [ fhir:value "Widow's peak" ]
  ], [
     fhir:index 427;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000444" ];
     fhir:CodeSystem.concept.display [ fhir:value "Convex nasal ridge" ]
  ], [
     fhir:index 428;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000506" ];
     fhir:CodeSystem.concept.display [ fhir:value "Telecanthus" ]
  ], [
     fhir:index 429;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000592" ];
     fhir:CodeSystem.concept.display [ fhir:value "Blue sclerae" ]
  ], [
     fhir:index 430;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000691" ];
     fhir:CodeSystem.concept.display [ fhir:value "Microdontia" ]
  ], [
     fhir:index 431;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000698" ];
     fhir:CodeSystem.concept.display [ fhir:value "Conical tooth" ]
  ], [
     fhir:index 432;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002000" ];
     fhir:CodeSystem.concept.display [ fhir:value "Short columella" ]
  ], [
     fhir:index 433;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002097" ];
     fhir:CodeSystem.concept.display [ fhir:value "Emphysema" ]
  ], [
     fhir:index 434;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002209" ];
     fhir:CodeSystem.concept.display [ fhir:value "Sparse scalp hair" ]
  ], [
     fhir:index 435;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002816" ];
     fhir:CodeSystem.concept.display [ fhir:value "Genu recurvatum" ]
  ], [
     fhir:index 436;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005116" ];
     fhir:CodeSystem.concept.display [ fhir:value "Arterial tortuosity" ]
  ], [
     fhir:index 437;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007957" ];
     fhir:CodeSystem.concept.display [ fhir:value "Corneal opacity" ]
  ], [
     fhir:index 438;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008070" ];
     fhir:CodeSystem.concept.display [ fhir:value "Sparse hair" ]
  ], [
     fhir:index 439;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009623" ];
     fhir:CodeSystem.concept.display [ fhir:value "Proximal placement of thumb" ]
  ], [
     fhir:index 440;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010055" ];
     fhir:CodeSystem.concept.display [ fhir:value "Broad hallux" ]
  ], [
     fhir:index 441;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011318" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bicoronal synostosis" ]
  ], [
     fhir:index 442;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011968" ];
     fhir:CodeSystem.concept.display [ fhir:value "Feeding difficulties" ]
  ], [
     fhir:index 443;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0200067" ];
     fhir:CodeSystem.concept.display [ fhir:value "Recurrent spontaneous abortion" ]
  ], [
     fhir:index 444;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011819" ];
     fhir:CodeSystem.concept.display [ fhir:value "Submucous cleft soft palate" ]
  ], [
     fhir:index 445;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000268" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dolichocephaly" ]
  ], [
     fhir:index 446;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003302" ];
     fhir:CodeSystem.concept.display [ fhir:value "Spondylolisthesis" ]
  ], [
     fhir:index 447;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000582" ];
     fhir:CodeSystem.concept.display [ fhir:value "Upslanted palpebral fissure" ]
  ], [
     fhir:index 448;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000952" ];
     fhir:CodeSystem.concept.display [ fhir:value "Jaundice" ]
  ], [
     fhir:index 449;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001298" ];
     fhir:CodeSystem.concept.display [ fhir:value "Encephalopathy" ]
  ], [
     fhir:index 450;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001396" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cholestasis" ]
  ], [
     fhir:index 451;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002059" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cerebral atrophy" ]
  ], [
     fhir:index 452;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002171" ];
     fhir:CodeSystem.concept.display [ fhir:value "Gliosis" ]
  ], [
     fhir:index 453;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002240" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hepatomegaly" ]
  ], [
     fhir:index 454;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002353" ];
     fhir:CodeSystem.concept.display [ fhir:value "EEG abnormality" ]
  ], [
     fhir:index 455;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002446" ];
     fhir:CodeSystem.concept.display [ fhir:value "Astrocytosis" ]
  ], [
     fhir:index 456;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003287" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of mitochondrial metabolism" ]
  ], [
     fhir:index 457;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011449" ];
     fhir:CodeSystem.concept.display [ fhir:value "Knee clonus" ]
  ], [
     fhir:index 458;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012852" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hepatic bridging fibrosis" ]
  ], [
     fhir:index 459;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100626" ];
     fhir:CodeSystem.concept.display [ fhir:value "Chronic hepatic failure" ]
  ], [
     fhir:index 460;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000385" ];
     fhir:CodeSystem.concept.display [ fhir:value "Small earlobe" ]
  ], [
     fhir:index 461;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009748" ];
     fhir:CodeSystem.concept.display [ fhir:value "Large earlobe" ]
  ], [
     fhir:index 462;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000157" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the tongue" ]
  ], [
     fhir:index 463;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000172" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the uvula" ]
  ], [
     fhir:index 464;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000174" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal palate morphology" ]
  ], [
     fhir:index 465;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000306" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the chin" ]
  ], [
     fhir:index 466;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004408" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the sense of smell" ]
  ], [
     fhir:index 467;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009912" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the tragus" ]
  ], [
     fhir:index 468;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000537" ];
     fhir:CodeSystem.concept.display [ fhir:value "Epicanthus inversus" ]
  ], [
     fhir:index 469;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000565" ];
     fhir:CodeSystem.concept.display [ fhir:value "Esotropia" ]
  ], [
     fhir:index 470;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000752" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyperactivity" ]
  ], [
     fhir:index 471;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003186" ];
     fhir:CodeSystem.concept.display [ fhir:value "Inverted nipples" ]
  ], [
     fhir:index 472;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012503" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the pituitary gland" ]
  ], [
     fhir:index 473;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100710" ];
     fhir:CodeSystem.concept.display [ fhir:value "Impulsivity" ]
  ], [
     fhir:index 474;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000357" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal location of ears" ]
  ], [
     fhir:index 475;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000820" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the thyroid gland" ]
  ], [
     fhir:index 476;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000828" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the parathyroid gland" ]
  ], [
     fhir:index 477;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000834" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the adrenal glands" ]
  ], [
     fhir:index 478;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012093" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of endocrine pancreas physiology" ]
  ], [
     fhir:index 479;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000269" ];
     fhir:CodeSystem.concept.display [ fhir:value "Prominent occiput" ]
  ], [
     fhir:index 480;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000535" ];
     fhir:CodeSystem.concept.display [ fhir:value "Sparse and thin eyebrow" ]
  ], [
     fhir:index 481;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000639" ];
     fhir:CodeSystem.concept.display [ fhir:value "Nystagmus" ]
  ], [
     fhir:index 482;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000718" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aggressive behavior" ]
  ], [
     fhir:index 483;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000957" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cafe-au-lait spot" ]
  ], [
     fhir:index 484;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000256" ];
     fhir:CodeSystem.concept.display [ fhir:value "Macrocephaly" ]
  ], [
     fhir:index 485;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000750" ];
     fhir:CodeSystem.concept.display [ fhir:value "Delayed speech and language development" ]
  ], [
     fhir:index 486;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000963" ];
     fhir:CodeSystem.concept.display [ fhir:value "Thin skin" ]
  ], [
     fhir:index 487;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001260" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dysarthria" ]
  ], [
     fhir:index 488;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002194" ];
     fhir:CodeSystem.concept.display [ fhir:value "Delayed gross motor development" ]
  ], [
     fhir:index 489;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003196" ];
     fhir:CodeSystem.concept.display [ fhir:value "Short nose" ]
  ], [
     fhir:index 490;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001155" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the hand" ]
  ], [
     fhir:index 491;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100022" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of movement" ]
  ], [
     fhir:index 492;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010862" ];
     fhir:CodeSystem.concept.display [ fhir:value "Delayed fine motor development" ]
  ], [
     fhir:index 493;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000343" ];
     fhir:CodeSystem.concept.display [ fhir:value "Long philtrum" ]
  ], [
     fhir:index 494;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000717" ];
     fhir:CodeSystem.concept.display [ fhir:value "Autism" ]
  ], [
     fhir:index 495;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001883" ];
     fhir:CodeSystem.concept.display [ fhir:value "Talipes" ]
  ], [
     fhir:index 496;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002553" ];
     fhir:CodeSystem.concept.display [ fhir:value "Highly arched eyebrow" ]
  ], [
     fhir:index 497;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007488" ];
     fhir:CodeSystem.concept.display [ fhir:value "Diffuse skin atrophy" ]
  ], [
     fhir:index 498;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000822" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypertension" ]
  ], [
     fhir:index 499;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001278" ];
     fhir:CodeSystem.concept.display [ fhir:value "Orthostatic hypotension" ]
  ], [
     fhir:index 500;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001944" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dehydration" ]
  ], [
     fhir:index 501;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001945" ];
     fhir:CodeSystem.concept.display [ fhir:value "Fever" ]
  ], [
     fhir:index 502;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002019" ];
     fhir:CodeSystem.concept.display [ fhir:value "Constipation" ]
  ], [
     fhir:index 503;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002020" ];
     fhir:CodeSystem.concept.display [ fhir:value "Gastroesophageal reflux" ]
  ], [
     fhir:index 504;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002027" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abdominal pain" ]
  ], [
     fhir:index 505;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002718" ];
     fhir:CodeSystem.concept.display [ fhir:value "Recurrent bacterial infections" ]
  ], [
     fhir:index 506;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002841" ];
     fhir:CodeSystem.concept.display [ fhir:value "Recurrent fungal infections" ]
  ], [
     fhir:index 507;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004395" ];
     fhir:CodeSystem.concept.display [ fhir:value "Malnutrition" ]
  ], [
     fhir:index 508;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009830" ];
     fhir:CodeSystem.concept.display [ fhir:value "Peripheral neuropathy" ]
  ], [
     fhir:index 509;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000126" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hydronephrosis" ]
  ], [
     fhir:index 510;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000519" ];
     fhir:CodeSystem.concept.display [ fhir:value "Developmental cataract" ]
  ], [
     fhir:index 511;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000648" ];
     fhir:CodeSystem.concept.display [ fhir:value "Optic atrophy" ]
  ], [
     fhir:index 512;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001053" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypopigmented skin patches" ]
  ], [
     fhir:index 513;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001087" ];
     fhir:CodeSystem.concept.display [ fhir:value "Developmental glaucoma" ]
  ], [
     fhir:index 514;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002119" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ventriculomegaly" ]
  ], [
     fhir:index 515;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002280" ];
     fhir:CodeSystem.concept.display [ fhir:value "Enlarged cisterna magna" ]
  ], [
     fhir:index 516;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003298" ];
     fhir:CodeSystem.concept.display [ fhir:value "Spina bifida occulta" ]
  ], [
     fhir:index 517;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004467" ];
     fhir:CodeSystem.concept.display [ fhir:value "Preauricular pit" ]
  ], [
     fhir:index 518;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008511" ];
     fhir:CodeSystem.concept.display [ fhir:value "Central posterior corneal opacity" ]
  ], [
     fhir:index 519;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010780" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyperacusis" ]
  ], [
     fhir:index 520;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030048" ];
     fhir:CodeSystem.concept.display [ fhir:value "Colpocephaly" ]
  ], [
     fhir:index 521;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100335" ];
     fhir:CodeSystem.concept.display [ fhir:value "Non-midline cleft lip" ]
  ], [
     fhir:index 522;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000525" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality iris morphology" ]
  ], [
     fhir:index 523;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002719" ];
     fhir:CodeSystem.concept.display [ fhir:value "Recurrent infections" ]
  ], [
     fhir:index 524;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000153" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the mouth" ]
  ], [
     fhir:index 525;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001903" ];
     fhir:CodeSystem.concept.display [ fhir:value "Anemia" ]
  ], [
     fhir:index 526;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002094" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dyspnea" ]
  ], [
     fhir:index 527;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002206" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pulmonary fibrosis" ]
  ], [
     fhir:index 528;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002789" ];
     fhir:CodeSystem.concept.display [ fhir:value "Tachypnea" ]
  ], [
     fhir:index 529;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002793" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal pattern of respiration" ]
  ], [
     fhir:index 530;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003565" ];
     fhir:CodeSystem.concept.display [ fhir:value "Elevated erythrocyte sedimentation rate" ]
  ], [
     fhir:index 531;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006517" ];
     fhir:CodeSystem.concept.display [ fhir:value "Intraalveolar phospholipid accumulation" ]
  ], [
     fhir:index 532;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006530" ];
     fhir:CodeSystem.concept.display [ fhir:value "Interstitial pulmonary abnormality" ]
  ], [
     fhir:index 533;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100759" ];
     fhir:CodeSystem.concept.display [ fhir:value "Clubbing of fingers" ]
  ], [
     fhir:index 534;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002103" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal pleura morphology" ]
  ], [
     fhir:index 535;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001596" ];
     fhir:CodeSystem.concept.display [ fhir:value "Alopecia" ]
  ], [
     fhir:index 536;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001882" ];
     fhir:CodeSystem.concept.display [ fhir:value "Leukopenia" ]
  ], [
     fhir:index 537;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002013" ];
     fhir:CodeSystem.concept.display [ fhir:value "Vomiting" ]
  ], [
     fhir:index 538;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002028" ];
     fhir:CodeSystem.concept.display [ fhir:value "Chronic diarrhea" ]
  ], [
     fhir:index 539;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002573" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hematochezia" ]
  ], [
     fhir:index 540;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002960" ];
     fhir:CodeSystem.concept.display [ fhir:value "Autoimmunity" ]
  ], [
     fhir:index 541;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005387" ];
     fhir:CodeSystem.concept.display [ fhir:value "Combined immunodeficiency" ]
  ], [
     fhir:index 542;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011109" ];
     fhir:CodeSystem.concept.display [ fhir:value "Chronic sinusitis" ]
  ], [
     fhir:index 543;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004429" ];
     fhir:CodeSystem.concept.display [ fhir:value "Recurrent viral infections" ]
  ], [
     fhir:index 544;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000280" ];
     fhir:CodeSystem.concept.display [ fhir:value "Coarse facial features" ]
  ], [
     fhir:index 545;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000294" ];
     fhir:CodeSystem.concept.display [ fhir:value "Low anterior hairline" ]
  ], [
     fhir:index 546;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000577" ];
     fhir:CodeSystem.concept.display [ fhir:value "Exotropia" ]
  ], [
     fhir:index 547;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001873" ];
     fhir:CodeSystem.concept.display [ fhir:value "Thrombocytopenia" ]
  ], [
     fhir:index 548;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002011" ];
     fhir:CodeSystem.concept.display [ fhir:value "Morphological central nervous system abnormality" ]
  ], [
     fhir:index 549;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006610" ];
     fhir:CodeSystem.concept.display [ fhir:value "Wide intermamillary distance" ]
  ], [
     fhir:index 550;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011231" ];
     fhir:CodeSystem.concept.display [ fhir:value "Prominent eyelashes" ]
  ], [
     fhir:index 551;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012718" ];
     fhir:CodeSystem.concept.display [ fhir:value "Morphological abnormality of the gastrointestinal tract" ]
  ], [
     fhir:index 552;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002024" ];
     fhir:CodeSystem.concept.display [ fhir:value "Malabsorption" ]
  ], [
     fhir:index 553;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001394" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cirrhosis" ]
  ], [
     fhir:index 554;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001414" ];
     fhir:CodeSystem.concept.display [ fhir:value "Microvesicular hepatic steatosis" ]
  ], [
     fhir:index 555;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001403" ];
     fhir:CodeSystem.concept.display [ fhir:value "Macrovesicular hepatic steatosis" ]
  ], [
     fhir:index 556;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001410" ];
     fhir:CodeSystem.concept.display [ fhir:value "Decreased liver function" ]
  ], [
     fhir:index 557;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001409" ];
     fhir:CodeSystem.concept.display [ fhir:value "Portal hypertension" ]
  ], [
     fhir:index 558;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001744" ];
     fhir:CodeSystem.concept.display [ fhir:value "Splenomegaly" ]
  ], [
     fhir:index 559;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003394" ];
     fhir:CodeSystem.concept.display [ fhir:value "Muscle spasm" ]
  ], [
     fhir:index 560;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003750" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased muscle fatiguability" ]
  ], [
     fhir:index 561;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002123" ];
     fhir:CodeSystem.concept.display [ fhir:value "Generalized myoclonic seizure" ]
  ], [
     fhir:index 562;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002219" ];
     fhir:CodeSystem.concept.display [ fhir:value "Facial hypertrichosis" ]
  ], [
     fhir:index 563;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000831" ];
     fhir:CodeSystem.concept.display [ fhir:value "Insulin-resistant diabetes mellitus" ]
  ], [
     fhir:index 564;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001891" ];
     fhir:CodeSystem.concept.display [ fhir:value "Iron deficiency anemia" ]
  ], [
     fhir:index 565;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001264" ];
     fhir:CodeSystem.concept.display [ fhir:value "Spastic diplegia" ]
  ], [
     fhir:index 566;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002313" ];
     fhir:CodeSystem.concept.display [ fhir:value "Spastic paraparesis" ]
  ], [
     fhir:index 567;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001347" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyperreflexia" ]
  ], [
     fhir:index 568;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002460" ];
     fhir:CodeSystem.concept.display [ fhir:value "Distal muscle weakness" ]
  ], [
     fhir:index 569;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000763" ];
     fhir:CodeSystem.concept.display [ fhir:value "Sensory neuropathy" ]
  ], [
     fhir:index 570;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001268" ];
     fhir:CodeSystem.concept.display [ fhir:value "Mental deterioration" ]
  ], [
     fhir:index 571;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002169" ];
     fhir:CodeSystem.concept.display [ fhir:value "Clonus" ]
  ], [
     fhir:index 572;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001332" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dystonia" ]
  ], [
     fhir:index 573;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100716" ];
     fhir:CodeSystem.concept.display [ fhir:value "Self-injurious behavior" ]
  ], [
     fhir:index 574;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000602" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ophthalmoplegia" ]
  ], [
     fhir:index 575;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001251" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ataxia" ]
  ], [
     fhir:index 576;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000776" ];
     fhir:CodeSystem.concept.display [ fhir:value "Congenital diaphragmatic hernia" ]
  ], [
     fhir:index 577;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000410" ];
     fhir:CodeSystem.concept.display [ fhir:value "Mixed hearing impairment" ]
  ], [
     fhir:index 578;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000510" ];
     fhir:CodeSystem.concept.display [ fhir:value "Rod-cone dystrophy" ]
  ], [
     fhir:index 579;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004437" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cranial hyperostosis" ]
  ], [
     fhir:index 580;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011001" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased bone mineral density" ]
  ], [
     fhir:index 581;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000956" ];
     fhir:CodeSystem.concept.display [ fhir:value "Acanthosis nigricans" ]
  ], [
     fhir:index 582;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000958" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dry skin" ]
  ], [
     fhir:index 583;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000580" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pigmentary retinopathy" ]
  ], [
     fhir:index 584;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000649" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of visual evoked potentials" ]
  ], [
     fhir:index 585;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000657" ];
     fhir:CodeSystem.concept.display [ fhir:value "Oculomotor apraxia" ]
  ], [
     fhir:index 586;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000479" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal retinal morphology" ]
  ], [
     fhir:index 587;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001317" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal cerebellum morphology" ]
  ], [
     fhir:index 588;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001533" ];
     fhir:CodeSystem.concept.display [ fhir:value "Slender build" ]
  ], [
     fhir:index 589;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001629" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ventricular septal defect" ]
  ], [
     fhir:index 590;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000703" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dentinogenesis imperfecta" ]
  ], [
     fhir:index 591;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000914" ];
     fhir:CodeSystem.concept.display [ fhir:value "Shield chest" ]
  ], [
     fhir:index 592;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001500" ];
     fhir:CodeSystem.concept.display [ fhir:value "Broad finger" ]
  ], [
     fhir:index 593;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003086" ];
     fhir:CodeSystem.concept.display [ fhir:value "Acromesomelia" ]
  ], [
     fhir:index 594;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003416" ];
     fhir:CodeSystem.concept.display [ fhir:value "Spinal canal stenosis" ]
  ], [
     fhir:index 595;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002815" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the knee" ]
  ], [
     fhir:index 596;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002992" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of tibia morphology" ]
  ], [
     fhir:index 597;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001639" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypertrophic cardiomyopathy" ]
  ], [
     fhir:index 598;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003236" ];
     fhir:CodeSystem.concept.display [ fhir:value "Elevated serum creatine kinase" ]
  ], [
     fhir:index 599;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001369" ];
     fhir:CodeSystem.concept.display [ fhir:value "Arthritis" ]
  ], [
     fhir:index 600;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003560" ];
     fhir:CodeSystem.concept.display [ fhir:value "Muscular dystrophy" ]
  ], [
     fhir:index 601;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003974" ];
     fhir:CodeSystem.concept.display [ fhir:value "Absent radius" ]
  ], [
     fhir:index 602;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002818" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the radius" ]
  ], [
     fhir:index 603;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001561" ];
     fhir:CodeSystem.concept.display [ fhir:value "Polyhydramnios" ]
  ], [
     fhir:index 604;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002299" ];
     fhir:CodeSystem.concept.display [ fhir:value "Brittle hair" ]
  ], [
     fhir:index 605;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002208" ];
     fhir:CodeSystem.concept.display [ fhir:value "Coarse hair" ]
  ], [
     fhir:index 606;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002213" ];
     fhir:CodeSystem.concept.display [ fhir:value "Fine hair" ]
  ], [
     fhir:index 607;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000522" ];
     fhir:CodeSystem.concept.display [ fhir:value "Alacrima" ]
  ], [
     fhir:index 608;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100704" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cerebral visual impairment" ]
  ], [
     fhir:index 609;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012713" ];
     fhir:CodeSystem.concept.display [ fhir:value "Moderate hearing impairment" ]
  ], [
     fhir:index 610;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002307" ];
     fhir:CodeSystem.concept.display [ fhir:value "Drooling" ]
  ], [
     fhir:index 611;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002714" ];
     fhir:CodeSystem.concept.display [ fhir:value "Downturned corners of mouth" ]
  ], [
     fhir:index 612;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000191" ];
     fhir:CodeSystem.concept.display [ fhir:value "Accessory oral frenulum" ]
  ], [
     fhir:index 613;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000158" ];
     fhir:CodeSystem.concept.display [ fhir:value "Macroglossia" ]
  ], [
     fhir:index 614;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012020" ];
     fhir:CodeSystem.concept.display [ fhir:value "Right aortic arch" ]
  ], [
     fhir:index 615;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002104" ];
     fhir:CodeSystem.concept.display [ fhir:value "Apnea" ]
  ], [
     fhir:index 616;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000598" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the ear" ]
  ], [
     fhir:index 617;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007874" ];
     fhir:CodeSystem.concept.display [ fhir:value "Almond-shaped palpebral fissure" ]
  ], [
     fhir:index 618;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010804" ];
     fhir:CodeSystem.concept.display [ fhir:value "Tented upper lip vermilion" ]
  ], [
     fhir:index 619;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000885" ];
     fhir:CodeSystem.concept.display [ fhir:value "Broad ribs" ]
  ], [
     fhir:index 620;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000768" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pectus carinatum" ]
  ], [
     fhir:index 621;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001680" ];
     fhir:CodeSystem.concept.display [ fhir:value "Coarctation of aorta" ]
  ], [
     fhir:index 622;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000687" ];
     fhir:CodeSystem.concept.display [ fhir:value "Widely spaced teeth" ]
  ], [
     fhir:index 623;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000047" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypospadias" ]
  ], [
     fhir:index 624;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001943" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoglycemia" ]
  ], [
     fhir:index 625;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012369" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of malar bones" ]
  ], [
     fhir:index 626;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009900" ];
     fhir:CodeSystem.concept.display [ fhir:value "Unilateral deafness" ]
  ], [
     fhir:index 627;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000023" ];
     fhir:CodeSystem.concept.display [ fhir:value "Inguinal hernia" ]
  ], [
     fhir:index 628;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000074" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ureteropelvic junction obstruction" ]
  ], [
     fhir:index 629;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001800" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoplastic toenails" ]
  ], [
     fhir:index 630;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001804" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoplastic fingernail" ]
  ], [
     fhir:index 631;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002949" ];
     fhir:CodeSystem.concept.display [ fhir:value "Fused cervical vertebrae" ]
  ], [
     fhir:index 632;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008050" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the palpebral fissures" ]
  ], [
     fhir:index 633;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008577" ];
     fhir:CodeSystem.concept.display [ fhir:value "Underfolded helix" ]
  ], [
     fhir:index 634;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008589" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoplastic helices" ]
  ], [
     fhir:index 635;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010863" ];
     fhir:CodeSystem.concept.display [ fhir:value "Receptive language delay" ]
  ], [
     fhir:index 636;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002282" ];
     fhir:CodeSystem.concept.display [ fhir:value "Gray matter heterotopia" ]
  ], [
     fhir:index 637;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002085" ];
     fhir:CodeSystem.concept.display [ fhir:value "Occipital encephalocele" ]
  ], [
     fhir:index 638;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001057" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aplasia cutis congenita" ]
  ], [
     fhir:index 639;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000211" ];
     fhir:CodeSystem.concept.display [ fhir:value "Trismus" ]
  ], [
     fhir:index 640;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008422" ];
     fhir:CodeSystem.concept.display [ fhir:value "Vertebral wedging" ]
  ], [
     fhir:index 641;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003170" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the acetabulum" ]
  ], [
     fhir:index 642;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003272" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the hip bone" ]
  ], [
     fhir:index 643;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003028" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the ankles" ]
  ], [
     fhir:index 644;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003301" ];
     fhir:CodeSystem.concept.display [ fhir:value "Irregular vertebral endplates" ]
  ], [
     fhir:index 645;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010508" ];
     fhir:CodeSystem.concept.display [ fhir:value "Metatarsus valgus" ]
  ], [
     fhir:index 646;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009811" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the elbow" ]
  ], [
     fhir:index 647;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000736" ];
     fhir:CodeSystem.concept.display [ fhir:value "Short attention span" ]
  ], [
     fhir:index 648;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002912" ];
     fhir:CodeSystem.concept.display [ fhir:value "Methylmalonic acidemia" ]
  ], [
     fhir:index 649;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001941" ];
     fhir:CodeSystem.concept.display [ fhir:value "Acidosis" ]
  ], [
     fhir:index 650;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001992" ];
     fhir:CodeSystem.concept.display [ fhir:value "Organic aciduria" ]
  ], [
     fhir:index 651;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009027" ];
     fhir:CodeSystem.concept.display [ fhir:value "Foot dorsiflexor weakness" ]
  ], [
     fhir:index 652;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002063" ];
     fhir:CodeSystem.concept.display [ fhir:value "Rigidity" ]
  ], [
     fhir:index 653;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000384" ];
     fhir:CodeSystem.concept.display [ fhir:value "Preauricular skin tag" ]
  ], [
     fhir:index 654;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0200046" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cat cry" ]
  ], [
     fhir:index 655;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001357" ];
     fhir:CodeSystem.concept.display [ fhir:value "Plagiocephaly" ]
  ], [
     fhir:index 656;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000670" ];
     fhir:CodeSystem.concept.display [ fhir:value "Carious teeth" ]
  ], [
     fhir:index 657;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011090" ];
     fhir:CodeSystem.concept.display [ fhir:value "Fused teeth" ]
  ], [
     fhir:index 658;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012810" ];
     fhir:CodeSystem.concept.display [ fhir:value "Wide nasal base" ]
  ], [
     fhir:index 659;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010296" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ankyloglossia" ]
  ], [
     fhir:index 660;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001636" ];
     fhir:CodeSystem.concept.display [ fhir:value "Tetralogy of Fallot" ]
  ], [
     fhir:index 661;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001305" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dandy-Walker malformation" ]
  ], [
     fhir:index 662;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000238" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hydrocephalus" ]
  ], [
     fhir:index 663;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005469" ];
     fhir:CodeSystem.concept.display [ fhir:value "Flat occiput" ]
  ], [
     fhir:index 664;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000270" ];
     fhir:CodeSystem.concept.display [ fhir:value "Delayed cranial suture closure" ]
  ], [
     fhir:index 665;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000239" ];
     fhir:CodeSystem.concept.display [ fhir:value "Large fontanelles" ]
  ], [
     fhir:index 666;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010537" ];
     fhir:CodeSystem.concept.display [ fhir:value "Wide cranial sutures" ]
  ], [
     fhir:index 667;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002217" ];
     fhir:CodeSystem.concept.display [ fhir:value "Slow-growing hair" ]
  ], [
     fhir:index 668;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000587" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the optic nerve" ]
  ], [
     fhir:index 669;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005989" ];
     fhir:CodeSystem.concept.display [ fhir:value "Redundant neck skin" ]
  ], [
     fhir:index 670;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010775" ];
     fhir:CodeSystem.concept.display [ fhir:value "Vascular ring" ]
  ], [
     fhir:index 671;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002779" ];
     fhir:CodeSystem.concept.display [ fhir:value "Tracheomalacia" ]
  ], [
     fhir:index 672;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002827" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hip dislocation" ]
  ], [
     fhir:index 673;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001302" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pachygyria" ]
  ], [
     fhir:index 674;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007362" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aplasia/Hypoplasia of the brainstem" ]
  ], [
     fhir:index 675;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001558" ];
     fhir:CodeSystem.concept.display [ fhir:value "Decreased fetal movement" ]
  ], [
     fhir:index 676;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010878" ];
     fhir:CodeSystem.concept.display [ fhir:value "Fetal cystic hygroma" ]
  ], [
     fhir:index 677;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011398" ];
     fhir:CodeSystem.concept.display [ fhir:value "Central hypotonia" ]
  ], [
     fhir:index 678;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002071" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of extrapyramidal motor function" ]
  ], [
     fhir:index 679;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000826" ];
     fhir:CodeSystem.concept.display [ fhir:value "Precocious puberty" ]
  ], [
     fhir:index 680;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000014" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the bladder" ]
  ], [
     fhir:index 681;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005037" ];
     fhir:CodeSystem.concept.display [ fhir:value "Proximal radio-ulnar synostosis" ]
  ], [
     fhir:index 682;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100543" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cognitive impairment" ]
  ], [
     fhir:index 683;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000481" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal cornea morphology" ]
  ], [
     fhir:index 684;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000076" ];
     fhir:CodeSystem.concept.display [ fhir:value "Vesicoureteral reflux" ]
  ], [
     fhir:index 685;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000297" ];
     fhir:CodeSystem.concept.display [ fhir:value "Facial hypotonia" ]
  ], [
     fhir:index 686;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000391" ];
     fhir:CodeSystem.concept.display [ fhir:value "Thickened helices" ]
  ], [
     fhir:index 687;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001162" ];
     fhir:CodeSystem.concept.display [ fhir:value "Postaxial hand polydactyly" ]
  ], [
     fhir:index 688;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001385" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hip dysplasia" ]
  ], [
     fhir:index 689;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002342" ];
     fhir:CodeSystem.concept.display [ fhir:value "Intellectual disability, moderate" ]
  ], [
     fhir:index 690;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003191" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cleft ala nasi" ]
  ], [
     fhir:index 691;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009765" ];
     fhir:CodeSystem.concept.display [ fhir:value "Low hanging columella" ]
  ], [
     fhir:index 692;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010297" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bifid tongue" ]
  ], [
     fhir:index 693;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011330" ];
     fhir:CodeSystem.concept.display [ fhir:value "Metopic synostosis" ]
  ], [
     fhir:index 694;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012804" ];
     fhir:CodeSystem.concept.display [ fhir:value "Corneal ulceration" ]
  ], [
     fhir:index 695;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010485" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyperextensibility at elbow" ]
  ], [
     fhir:index 696;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000609" ];
     fhir:CodeSystem.concept.display [ fhir:value "Optic nerve hypoplasia" ]
  ], [
     fhir:index 697;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001176" ];
     fhir:CodeSystem.concept.display [ fhir:value "Large hands" ]
  ], [
     fhir:index 698;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004233" ];
     fhir:CodeSystem.concept.display [ fhir:value "Advanced ossification of carpal bones" ]
  ], [
     fhir:index 699;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100842" ];
     fhir:CodeSystem.concept.display [ fhir:value "Septo-optic dysplasia" ]
  ], [
     fhir:index 700;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002034" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the rectum" ]
  ], [
     fhir:index 701;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002283" ];
     fhir:CodeSystem.concept.display [ fhir:value "Global brain atrophy" ]
  ], [
     fhir:index 702;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003115" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal EKG" ]
  ], [
     fhir:index 703;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002577" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal stomach morphology" ]
  ], [
     fhir:index 704;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002539" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cortical dysplasia" ]
  ], [
     fhir:index 705;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006818" ];
     fhir:CodeSystem.concept.display [ fhir:value "4-layered lissencephaly" ]
  ], [
     fhir:index 706;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000593" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal anterior chamber morphology" ]
  ], [
     fhir:index 707;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000179" ];
     fhir:CodeSystem.concept.display [ fhir:value "Thick lower lip vermilion" ]
  ], [
     fhir:index 708;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002002" ];
     fhir:CodeSystem.concept.display [ fhir:value "Deep philtrum" ]
  ], [
     fhir:index 709;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009931" ];
     fhir:CodeSystem.concept.display [ fhir:value "Enlarged naris" ]
  ], [
     fhir:index 710;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002948" ];
     fhir:CodeSystem.concept.display [ fhir:value "Vertebral fusion" ]
  ], [
     fhir:index 711;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002937" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hemivertebrae" ]
  ], [
     fhir:index 712;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002308" ];
     fhir:CodeSystem.concept.display [ fhir:value "Arnold-Chiari malformation" ]
  ], [
     fhir:index 713;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011320" ];
     fhir:CodeSystem.concept.display [ fhir:value "Unilambdoid synostosis" ]
  ], [
     fhir:index 714;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002781" ];
     fhir:CodeSystem.concept.display [ fhir:value "Upper airway obstruction" ]
  ], [
     fhir:index 715;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001363" ];
     fhir:CodeSystem.concept.display [ fhir:value "Craniosynostosis" ]
  ], [
     fhir:index 716;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000204" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cleft upper lip" ]
  ], [
     fhir:index 717;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001738" ];
     fhir:CodeSystem.concept.display [ fhir:value "Exocrine pancreatic insufficiency" ]
  ], [
     fhir:index 718;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002823" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of femur morphology" ]
  ], [
     fhir:index 719;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000823" ];
     fhir:CodeSystem.concept.display [ fhir:value "Delayed puberty" ]
  ], [
     fhir:index 720;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100279" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ulcerative colitis" ]
  ], [
     fhir:index 721;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003834" ];
     fhir:CodeSystem.concept.display [ fhir:value "Shoulder dislocation" ]
  ], [
     fhir:index 722;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001065" ];
     fhir:CodeSystem.concept.display [ fhir:value "Striae distensae" ]
  ], [
     fhir:index 723;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000448" ];
     fhir:CodeSystem.concept.display [ fhir:value "Prominent nose" ]
  ], [
     fhir:index 724;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000554" ];
     fhir:CodeSystem.concept.display [ fhir:value "Uveitis" ]
  ], [
     fhir:index 725;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001006" ];
     fhir:CodeSystem.concept.display [ fhir:value "obsolete Hypotrichosis" ]
  ], [
     fhir:index 726;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000501" ];
     fhir:CodeSystem.concept.display [ fhir:value "Glaucoma" ]
  ], [
     fhir:index 727;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000262" ];
     fhir:CodeSystem.concept.display [ fhir:value "Turricephaly" ]
  ], [
     fhir:index 728;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000729" ];
     fhir:CodeSystem.concept.display [ fhir:value "Autistic behavior" ]
  ], [
     fhir:index 729;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010800" ];
     fhir:CodeSystem.concept.display [ fhir:value "Absent cupid's bow" ]
  ], [
     fhir:index 730;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010808" ];
     fhir:CodeSystem.concept.display [ fhir:value "Protruding tongue" ]
  ], [
     fhir:index 731;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009927" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aplasia of the nose" ]
  ], [
     fhir:index 732;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100539" ];
     fhir:CodeSystem.concept.display [ fhir:value "Periorbital edema" ]
  ], [
     fhir:index 733;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000629" ];
     fhir:CodeSystem.concept.display [ fhir:value "Periorbital fullness" ]
  ], [
     fhir:index 734;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000178" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of lower lip" ]
  ], [
     fhir:index 735;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000168" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the gingiva" ]
  ], [
     fhir:index 736;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001022" ];
     fhir:CodeSystem.concept.display [ fhir:value "Albinism" ]
  ], [
     fhir:index 737;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000177" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of upper lip" ]
  ], [
     fhir:index 738;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001337" ];
     fhir:CodeSystem.concept.display [ fhir:value "Tremor" ]
  ], [
     fhir:index 739;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002135" ];
     fhir:CodeSystem.concept.display [ fhir:value "Basal ganglia calcification" ]
  ], [
     fhir:index 740;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002352" ];
     fhir:CodeSystem.concept.display [ fhir:value "Leukoencephalopathy" ]
  ], [
     fhir:index 741;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002514" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cerebral calcification" ]
  ], [
     fhir:index 742;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010576" ];
     fhir:CodeSystem.concept.display [ fhir:value "Intracranial cystic lesion" ]
  ], [
     fhir:index 743;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001622" ];
     fhir:CodeSystem.concept.display [ fhir:value "Premature birth" ]
  ], [
     fhir:index 744;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002415" ];
     fhir:CodeSystem.concept.display [ fhir:value "Leukodystrophy" ]
  ], [
     fhir:index 745;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001320" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cerebellar vermis hypoplasia" ]
  ], [
     fhir:index 746;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001773" ];
     fhir:CodeSystem.concept.display [ fhir:value "Short foot" ]
  ], [
     fhir:index 747;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002750" ];
     fhir:CodeSystem.concept.display [ fhir:value "Delayed skeletal maturation" ]
  ], [
     fhir:index 748;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004415" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pulmonary artery stenosis" ]
  ], [
     fhir:index 749;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012741" ];
     fhir:CodeSystem.concept.display [ fhir:value "Unilateral cryptorchidism" ]
  ], [
     fhir:index 750;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000036" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the penis" ]
  ], [
     fhir:index 751;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002408" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cerebral arteriovenous malformation" ]
  ], [
     fhir:index 752;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007457" ];
     fhir:CodeSystem.concept.display [ fhir:value "Prominent veins on trunk" ]
  ], [
     fhir:index 753;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000378" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cupped ear" ]
  ], [
     fhir:index 754;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000396" ];
     fhir:CodeSystem.concept.display [ fhir:value "Overfolded helix" ]
  ], [
     fhir:index 755;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000035" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal testis morphology" ]
  ], [
     fhir:index 756;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009895" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the crus of the helix" ]
  ], [
     fhir:index 757;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000034" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hydrocele testis" ]
  ], [
     fhir:index 758;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000722" ];
     fhir:CodeSystem.concept.display [ fhir:value "Obsessive-compulsive behavior" ]
  ], [
     fhir:index 759;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000845" ];
     fhir:CodeSystem.concept.display [ fhir:value "Growth hormone excess" ]
  ], [
     fhir:index 760;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100829" ];
     fhir:CodeSystem.concept.display [ fhir:value "Galactorrhea" ]
  ], [
     fhir:index 761;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001578" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased circulating cortisol level" ]
  ], [
     fhir:index 762;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000786" ];
     fhir:CodeSystem.concept.display [ fhir:value "Primary amenorrhea" ]
  ], [
     fhir:index 763;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001701" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pericarditis" ]
  ], [
     fhir:index 764;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002076" ];
     fhir:CodeSystem.concept.display [ fhir:value "Migraine" ]
  ], [
     fhir:index 765;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004755" ];
     fhir:CodeSystem.concept.display [ fhir:value "Supraventricular tachycardia" ]
  ], [
     fhir:index 766;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010522" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dyslexia" ]
  ], [
     fhir:index 767;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004313" ];
     fhir:CodeSystem.concept.display [ fhir:value "Decreased circulating antibody level" ]
  ], [
     fhir:index 768;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000011" ];
     fhir:CodeSystem.concept.display [ fhir:value "Neurogenic bladder" ]
  ], [
     fhir:index 769;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000641" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dysmetric saccades" ]
  ], [
     fhir:index 770;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007772" ];
     fhir:CodeSystem.concept.display [ fhir:value "Impaired smooth pursuit" ]
  ], [
     fhir:index 771;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001583" ];
     fhir:CodeSystem.concept.display [ fhir:value "Rotary nystagmus" ]
  ], [
     fhir:index 772;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010544" ];
     fhir:CodeSystem.concept.display [ fhir:value "Vertical nystagmus" ]
  ], [
     fhir:index 773;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012735" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cough" ]
  ], [
     fhir:index 774;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002075" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dysdiadochokinesis" ]
  ], [
     fhir:index 775;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007256" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal pyramidal sign" ]
  ], [
     fhir:index 776;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001257" ];
     fhir:CodeSystem.concept.display [ fhir:value "Spasticity" ]
  ], [
     fhir:index 777;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002321" ];
     fhir:CodeSystem.concept.display [ fhir:value "Vertigo" ]
  ], [
     fhir:index 778;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002384" ];
     fhir:CodeSystem.concept.display [ fhir:value "Focal impaired awareness seizure" ]
  ], [
     fhir:index 779;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011376" ];
     fhir:CodeSystem.concept.display [ fhir:value "Morphological abnormality of the vestibule of the inner ear" ]
  ], [
     fhir:index 780;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002326" ];
     fhir:CodeSystem.concept.display [ fhir:value "Transient ischemic attack" ]
  ], [
     fhir:index 781;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005584" ];
     fhir:CodeSystem.concept.display [ fhir:value "Renal cell carcinoma" ]
  ], [
     fhir:index 782;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003124" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypercholesterolemia" ]
  ], [
     fhir:index 783;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003002" ];
     fhir:CodeSystem.concept.display [ fhir:value "Breast carcinoma" ]
  ], [
     fhir:index 784;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004953" ];
     fhir:CodeSystem.concept.display [ fhir:value "obsolete Dilatation of abdominal aorta" ]
  ], [
     fhir:index 785;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004944" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dilatation of the cerebral artery" ]
  ], [
     fhir:index 786;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000100" ];
     fhir:CodeSystem.concept.display [ fhir:value "Nephrotic syndrome" ]
  ], [
     fhir:index 787;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002783" ];
     fhir:CodeSystem.concept.display [ fhir:value "Recurrent lower respiratory tract infections" ]
  ], [
     fhir:index 788;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003470" ];
     fhir:CodeSystem.concept.display [ fhir:value "Paralysis" ]
  ], [
     fhir:index 789;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006597" ];
     fhir:CodeSystem.concept.display [ fhir:value "Diaphragmatic paralysis" ]
  ], [
     fhir:index 790;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008151" ];
     fhir:CodeSystem.concept.display [ fhir:value "Prolonged prothrombin time" ]
  ], [
     fhir:index 791;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010628" ];
     fhir:CodeSystem.concept.display [ fhir:value "Facial palsy" ]
  ], [
     fhir:index 792;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011892" ];
     fhir:CodeSystem.concept.display [ fhir:value "Low levels of vitamin K" ]
  ], [
     fhir:index 793;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001075" ];
     fhir:CodeSystem.concept.display [ fhir:value "Atrophic scars" ]
  ], [
     fhir:index 794;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001816" ];
     fhir:CodeSystem.concept.display [ fhir:value "Thin nail" ]
  ], [
     fhir:index 795;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002216" ];
     fhir:CodeSystem.concept.display [ fhir:value "Premature graying of hair" ]
  ], [
     fhir:index 796;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003401" ];
     fhir:CodeSystem.concept.display [ fhir:value "Paresthesia" ]
  ], [
     fhir:index 797;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100134" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the axillary hair" ]
  ], [
     fhir:index 798;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100797" ];
     fhir:CodeSystem.concept.display [ fhir:value "Toenail dysplasia" ]
  ], [
     fhir:index 799;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010461" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the male genitalia" ]
  ], [
     fhir:index 800;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000044" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypogonadotropic hypogonadism" ]
  ], [
     fhir:index 801;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100568" ];
     fhir:CodeSystem.concept.display [ fhir:value "Neoplasm of the endocrine system" ]
  ], [
     fhir:index 802;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001646" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal aortic valve morphology" ]
  ], [
     fhir:index 803;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000813" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bicornuate uterus" ]
  ], [
     fhir:index 804;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004380" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aortic valve calcification" ]
  ], [
     fhir:index 805;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001650" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aortic valve stenosis" ]
  ], [
     fhir:index 806;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000073" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ureteral duplication" ]
  ], [
     fhir:index 807;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100651" ];
     fhir:CodeSystem.concept.display [ fhir:value "Type I diabetes mellitus" ]
  ], [
     fhir:index 808;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000819" ];
     fhir:CodeSystem.concept.display [ fhir:value "Diabetes mellitus" ]
  ], [
     fhir:index 809;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000573" ];
     fhir:CodeSystem.concept.display [ fhir:value "Retinal hemorrhage" ]
  ], [
     fhir:index 810;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005264" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the gallbladder" ]
  ], [
     fhir:index 811;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000475" ];
     fhir:CodeSystem.concept.display [ fhir:value "Broad neck" ]
  ], [
     fhir:index 812;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000089" ];
     fhir:CodeSystem.concept.display [ fhir:value "Renal hypoplasia" ]
  ], [
     fhir:index 813;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000921" ];
     fhir:CodeSystem.concept.display [ fhir:value "Missing ribs" ]
  ], [
     fhir:index 814;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001789" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hydrops fetalis" ]
  ], [
     fhir:index 815;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002089" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pulmonary hypoplasia" ]
  ], [
     fhir:index 816;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003422" ];
     fhir:CodeSystem.concept.display [ fhir:value "Vertebral segmentation defect" ]
  ], [
     fhir:index 817;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002323" ];
     fhir:CodeSystem.concept.display [ fhir:value "Anencephaly" ]
  ], [
     fhir:index 818;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000341" ];
     fhir:CodeSystem.concept.display [ fhir:value "Narrow forehead" ]
  ], [
     fhir:index 819;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002869" ];
     fhir:CodeSystem.concept.display [ fhir:value "Flared iliac wings" ]
  ], [
     fhir:index 820;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003100" ];
     fhir:CodeSystem.concept.display [ fhir:value "Slender long bone" ]
  ], [
     fhir:index 821;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003275" ];
     fhir:CodeSystem.concept.display [ fhir:value "Narrow pelvis bone" ]
  ], [
     fhir:index 822;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009891" ];
     fhir:CodeSystem.concept.display [ fhir:value "Underdeveloped supraorbital ridges" ]
  ], [
     fhir:index 823;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011039" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the helix" ]
  ], [
     fhir:index 824;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008572" ];
     fhir:CodeSystem.concept.display [ fhir:value "External ear malformation" ]
  ], [
     fhir:index 825;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009738" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the antihelix" ]
  ], [
     fhir:index 826;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011328" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of fontanelles" ]
  ], [
     fhir:index 827;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012155" ];
     fhir:CodeSystem.concept.display [ fhir:value "Decreased corneal sensation" ]
  ], [
     fhir:index 828;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004602" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cervical C2/C3 vertebral fusion" ]
  ], [
     fhir:index 829;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002997" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the ulna" ]
  ], [
     fhir:index 830;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009777" ];
     fhir:CodeSystem.concept.display [ fhir:value "Absent thumb" ]
  ], [
     fhir:index 831;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002893" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pituitary adenoma" ]
  ], [
     fhir:index 832;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0040278" ];
     fhir:CodeSystem.concept.display [ fhir:value "Prolactinoma" ]
  ], [
     fhir:index 833;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001555" ];
     fhir:CodeSystem.concept.display [ fhir:value "Asymmetry of the thorax" ]
  ], [
     fhir:index 834;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000902" ];
     fhir:CodeSystem.concept.display [ fhir:value "Rib fusion" ]
  ], [
     fhir:index 835;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002164" ];
     fhir:CodeSystem.concept.display [ fhir:value "Nail dysplasia" ]
  ], [
     fhir:index 836;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011314" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of long bone morphology" ]
  ], [
     fhir:index 837;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002867" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the ilium" ]
  ], [
     fhir:index 838;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000774" ];
     fhir:CodeSystem.concept.display [ fhir:value "Narrow chest" ]
  ], [
     fhir:index 839;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006482" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of dental morphology" ]
  ], [
     fhir:index 840;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004383" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoplastic left heart" ]
  ], [
     fhir:index 841;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002015" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dysphagia" ]
  ], [
     fhir:index 842;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0500093" ];
     fhir:CodeSystem.concept.display [ fhir:value "Food allergy" ]
  ], [
     fhir:index 843;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001519" ];
     fhir:CodeSystem.concept.display [ fhir:value "Disproportionate tall stature" ]
  ], [
     fhir:index 844;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003179" ];
     fhir:CodeSystem.concept.display [ fhir:value "Protrusio acetabuli" ]
  ], [
     fhir:index 845;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007385" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aplasia cutis congenita of scalp" ]
  ], [
     fhir:index 846;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000716" ];
     fhir:CodeSystem.concept.display [ fhir:value "Depressivity" ]
  ], [
     fhir:index 847;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012583" ];
     fhir:CodeSystem.concept.display [ fhir:value "Unilateral renal hypoplasia" ]
  ], [
     fhir:index 848;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000618" ];
     fhir:CodeSystem.concept.display [ fhir:value "Blindness" ]
  ], [
     fhir:index 849;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001004" ];
     fhir:CodeSystem.concept.display [ fhir:value "Lymphedema" ]
  ], [
     fhir:index 850;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002652" ];
     fhir:CodeSystem.concept.display [ fhir:value "Skeletal dysplasia" ]
  ], [
     fhir:index 851;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012520" ];
     fhir:CodeSystem.concept.display [ fhir:value "Perivascular spaces" ]
  ], [
     fhir:index 852;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005293" ];
     fhir:CodeSystem.concept.display [ fhir:value "Venous insufficiency" ]
  ], [
     fhir:index 853;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012432" ];
     fhir:CodeSystem.concept.display [ fhir:value "Chronic fatigue" ]
  ], [
     fhir:index 854;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002578" ];
     fhir:CodeSystem.concept.display [ fhir:value "Gastroparesis" ]
  ], [
     fhir:index 855;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001658" ];
     fhir:CodeSystem.concept.display [ fhir:value "Myocardial infarction" ]
  ], [
     fhir:index 856;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001802" ];
     fhir:CodeSystem.concept.display [ fhir:value "Absent toenail" ]
  ], [
     fhir:index 857;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001821" ];
     fhir:CodeSystem.concept.display [ fhir:value "Broad nail" ]
  ], [
     fhir:index 858;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000807" ];
     fhir:CodeSystem.concept.display [ fhir:value "Glandular hypospadias" ]
  ], [
     fhir:index 859;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100582" ];
     fhir:CodeSystem.concept.display [ fhir:value "Nasal polyposis" ]
  ], [
     fhir:index 860;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002653" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bone pain" ]
  ], [
     fhir:index 861;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001073" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cigarette-paper scars" ]
  ], [
     fhir:index 862;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0031913" ];
     fhir:CodeSystem.concept.display [ fhir:value "Rhombencephalosynapsis" ]
  ], [
     fhir:index 863;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002617" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dilatation" ]
  ], [
     fhir:index 864;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005107" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal sacrum morphology" ]
  ], [
     fhir:index 865;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002025" ];
     fhir:CodeSystem.concept.display [ fhir:value "Anal stenosis" ]
  ], [
     fhir:index 866;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009099" ];
     fhir:CodeSystem.concept.display [ fhir:value "Median cleft palate" ]
  ], [
     fhir:index 867;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003212" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased circulating IgE level" ]
  ], [
     fhir:index 868;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001319" ];
     fhir:CodeSystem.concept.display [ fhir:value "Neonatal hypotonia" ]
  ], [
     fhir:index 869;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002659" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased susceptibility to fractures" ]
  ], [
     fhir:index 870;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0025246" ];
     fhir:CodeSystem.concept.display [ fhir:value "Trichilemmal cyst" ]
  ], [
     fhir:index 871;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002107" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pneumothorax" ]
  ], [
     fhir:index 872;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000107" ];
     fhir:CodeSystem.concept.display [ fhir:value "Renal cyst" ]
  ], [
     fhir:index 873;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001025" ];
     fhir:CodeSystem.concept.display [ fhir:value "Urticaria" ]
  ], [
     fhir:index 874;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002204" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pulmonary embolism" ]
  ], [
     fhir:index 875;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001058" ];
     fhir:CodeSystem.concept.display [ fhir:value "Poor wound healing" ]
  ], [
     fhir:index 876;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003010" ];
     fhir:CodeSystem.concept.display [ fhir:value "Prolonged bleeding time" ]
  ], [
     fhir:index 877;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100502" ];
     fhir:CodeSystem.concept.display [ fhir:value "Vitamin B12 deficiency" ]
  ], [
     fhir:index 878;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100510" ];
     fhir:CodeSystem.concept.display [ fhir:value "Low levels of vitamin C" ]
  ], [
     fhir:index 879;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030976" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal factor VIII activity" ]
  ], [
     fhir:index 880;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100789" ];
     fhir:CodeSystem.concept.display [ fhir:value "Torus palatinus" ]
  ], [
     fhir:index 881;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000108" ];
     fhir:CodeSystem.concept.display [ fhir:value "Renal corticomedullary cysts" ]
  ], [
     fhir:index 882;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000072" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hydroureter" ]
  ], [
     fhir:index 883;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000019" ];
     fhir:CodeSystem.concept.display [ fhir:value "Urinary hesitancy" ]
  ], [
     fhir:index 884;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100771" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoperistalsis" ]
  ], [
     fhir:index 885;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000021" ];
     fhir:CodeSystem.concept.display [ fhir:value "Megacystis" ]
  ], [
     fhir:index 886;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004388" ];
     fhir:CodeSystem.concept.display [ fhir:value "Microcolon" ]
  ], [
     fhir:index 887;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005247" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoplasia of the abdominal wall musculature" ]
  ], [
     fhir:index 888;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004794" ];
     fhir:CodeSystem.concept.display [ fhir:value "Malrotation of small bowel" ]
  ], [
     fhir:index 889;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000045" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the scrotum" ]
  ], [
     fhir:index 890;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002236" ];
     fhir:CodeSystem.concept.display [ fhir:value "Frontal upsweep of hair" ]
  ], [
     fhir:index 891;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000212" ];
     fhir:CodeSystem.concept.display [ fhir:value "Gingival overgrowth" ]
  ], [
     fhir:index 892;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001808" ];
     fhir:CodeSystem.concept.display [ fhir:value "Fragile nails" ]
  ], [
     fhir:index 893;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000225" ];
     fhir:CodeSystem.concept.display [ fhir:value "Gingival bleeding" ]
  ], [
     fhir:index 894;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006009" ];
     fhir:CodeSystem.concept.display [ fhir:value "Broad phalanx" ]
  ], [
     fhir:index 895;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001837" ];
     fhir:CodeSystem.concept.display [ fhir:value "Broad toe" ]
  ], [
     fhir:index 896;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001946" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ketosis" ]
  ], [
     fhir:index 897;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002490" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased CSF lactate" ]
  ], [
     fhir:index 898;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002922" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased CSF protein" ]
  ], [
     fhir:index 899;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003128" ];
     fhir:CodeSystem.concept.display [ fhir:value "Lactic acidosis" ]
  ], [
     fhir:index 900;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003111" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal blood ion concentration" ]
  ], [
     fhir:index 901;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0032234" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased circulating creatine kinase MM isoform" ]
  ], [
     fhir:index 902;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003348" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyperalaninemia" ]
  ], [
     fhir:index 903;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008347" ];
     fhir:CodeSystem.concept.display [ fhir:value "Decreased activity of mitochondrial complex IV" ]
  ], [
     fhir:index 904;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000326" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the maxilla" ]
  ], [
     fhir:index 905;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010758" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the premaxilla" ]
  ], [
     fhir:index 906;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005681" ];
     fhir:CodeSystem.concept.display [ fhir:value "Juvenile rheumatoid arthritis" ]
  ], [
     fhir:index 907;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000514" ];
     fhir:CodeSystem.concept.display [ fhir:value "Slow saccadic eye movements" ]
  ], [
     fhir:index 908;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002788" ];
     fhir:CodeSystem.concept.display [ fhir:value "Recurrent upper respiratory tract infections" ]
  ], [
     fhir:index 909;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003396" ];
     fhir:CodeSystem.concept.display [ fhir:value "Syringomyelia" ]
  ], [
     fhir:index 910;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003011" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the musculature" ]
  ], [
     fhir:index 911;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002098" ];
     fhir:CodeSystem.concept.display [ fhir:value "Respiratory distress" ]
  ], [
     fhir:index 912;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002018" ];
     fhir:CodeSystem.concept.display [ fhir:value "Nausea" ]
  ], [
     fhir:index 913;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002014" ];
     fhir:CodeSystem.concept.display [ fhir:value "Diarrhea" ]
  ], [
     fhir:index 914;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0025168" ];
     fhir:CodeSystem.concept.display [ fhir:value "Left ventricular diastolic dysfunction" ]
  ], [
     fhir:index 915;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001679" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal aortic morphology" ]
  ], [
     fhir:index 916;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000159" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal lip morphology" ]
  ], [
     fhir:index 917;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011338" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of mouth shape" ]
  ], [
     fhir:index 918;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000478" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the eye" ]
  ], [
     fhir:index 919;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000154" ];
     fhir:CodeSystem.concept.display [ fhir:value "Wide mouth" ]
  ], [
     fhir:index 920;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001513" ];
     fhir:CodeSystem.concept.display [ fhir:value "Obesity" ]
  ], [
     fhir:index 921;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002475" ];
     fhir:CodeSystem.concept.display [ fhir:value "Myelomeningocele" ]
  ], [
     fhir:index 922;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003765" ];
     fhir:CodeSystem.concept.display [ fhir:value "Psoriasiform dermatitis" ]
  ], [
     fhir:index 923;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010289" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cleft of alveolar ridge of maxilla" ]
  ], [
     fhir:index 924;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003908" ];
     fhir:CodeSystem.concept.display [ fhir:value "Corner fracture of metaphysis" ]
  ], [
     fhir:index 925;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002190" ];
     fhir:CodeSystem.concept.display [ fhir:value "Choroid plexus cyst" ]
  ], [
     fhir:index 926;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004370" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of temperature regulation" ]
  ], [
     fhir:index 927;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011611" ];
     fhir:CodeSystem.concept.display [ fhir:value "Interrupted aortic arch" ]
  ], [
     fhir:index 928;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000737" ];
     fhir:CodeSystem.concept.display [ fhir:value "Irritability" ]
  ], [
     fhir:index 929;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001344" ];
     fhir:CodeSystem.concept.display [ fhir:value "Absent speech" ]
  ], [
     fhir:index 930;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002376" ];
     fhir:CodeSystem.concept.display [ fhir:value "Developmental regression" ]
  ], [
     fhir:index 931;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002140" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ischemic stroke" ]
  ], [
     fhir:index 932;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001287" ];
     fhir:CodeSystem.concept.display [ fhir:value "Meningitis" ]
  ], [
     fhir:index 933;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002721" ];
     fhir:CodeSystem.concept.display [ fhir:value "Immunodeficiency" ]
  ], [
     fhir:index 934;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000041" ];
     fhir:CodeSystem.concept.display [ fhir:value "Chordee" ]
  ], [
     fhir:index 935;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012854" ];
     fhir:CodeSystem.concept.display [ fhir:value "Midshaft hypospadias" ]
  ], [
     fhir:index 936;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000808" ];
     fhir:CodeSystem.concept.display [ fhir:value "Penoscrotal hypospadias" ]
  ], [
     fhir:index 937;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000048" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bifid scrotum" ]
  ], [
     fhir:index 938;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001047" ];
     fhir:CodeSystem.concept.display [ fhir:value "Atopic dermatitis" ]
  ], [
     fhir:index 939;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001621" ];
     fhir:CodeSystem.concept.display [ fhir:value "Weak voice" ]
  ], [
     fhir:index 940;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002372" ];
     fhir:CodeSystem.concept.display [ fhir:value "Normal interictal EEG" ]
  ], [
     fhir:index 941;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012803" ];
     fhir:CodeSystem.concept.display [ fhir:value "Anisometropia" ]
  ], [
     fhir:index 942;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011386" ];
     fhir:CodeSystem.concept.display [ fhir:value "Narrow internal auditory canal" ]
  ], [
     fhir:index 943;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012714" ];
     fhir:CodeSystem.concept.display [ fhir:value "Severe hearing impairment" ]
  ], [
     fhir:index 944;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006485" ];
     fhir:CodeSystem.concept.display [ fhir:value "Agenesis of incisor" ]
  ], [
     fhir:index 945;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000787" ];
     fhir:CodeSystem.concept.display [ fhir:value "Nephrolithiasis" ]
  ], [
     fhir:index 946;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011332" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hemifacial hypoplasia" ]
  ], [
     fhir:index 947;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001909" ];
     fhir:CodeSystem.concept.display [ fhir:value "Leukemia" ]
  ], [
     fhir:index 948;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004808" ];
     fhir:CodeSystem.concept.display [ fhir:value "Acute myeloid leukemia" ]
  ], [
     fhir:index 949;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006495" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aplasia/Hypoplasia of the ulna" ]
  ], [
     fhir:index 950;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001180" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hand oligodactyly" ]
  ], [
     fhir:index 951;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002991" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of fibula morphology" ]
  ], [
     fhir:index 952;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001849" ];
     fhir:CodeSystem.concept.display [ fhir:value "Foot oligodactyly" ]
  ], [
     fhir:index 953;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006507" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aplasia/hypoplasia of the humerus" ]
  ], [
     fhir:index 954;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005613" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aplasia/hypoplasia of the femur" ]
  ], [
     fhir:index 955;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006492" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aplasia/Hypoplasia of the fibula" ]
  ], [
     fhir:index 956;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000098" ];
     fhir:CodeSystem.concept.display [ fhir:value "Tall stature" ]
  ], [
     fhir:index 957;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003311" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoplasia of the odontoid process" ]
  ], [
     fhir:index 958;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005752" ];
     fhir:CodeSystem.concept.display [ fhir:value "Flattened moderately deformed vertebrae" ]
  ], [
     fhir:index 959;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030039" ];
     fhir:CodeSystem.concept.display [ fhir:value "Fused thoracic vertebrae" ]
  ], [
     fhir:index 960;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003304" ];
     fhir:CodeSystem.concept.display [ fhir:value "Spondylolysis" ]
  ], [
     fhir:index 961;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001659" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aortic regurgitation" ]
  ], [
     fhir:index 962;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002984" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoplasia of the radius" ]
  ], [
     fhir:index 963;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009944" ];
     fhir:CodeSystem.concept.display [ fhir:value "Partial duplication of thumb phalanx" ]
  ], [
     fhir:index 964;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005819" ];
     fhir:CodeSystem.concept.display [ fhir:value "Short middle phalanx of finger" ]
  ], [
     fhir:index 965;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002110" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bronchiectasis" ]
  ], [
     fhir:index 966;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001677" ];
     fhir:CodeSystem.concept.display [ fhir:value "Coronary artery atherosclerosis" ]
  ], [
     fhir:index 967;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001737" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pancreatic cysts" ]
  ], [
     fhir:index 968;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005113" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aortic arch aneurysm" ]
  ], [
     fhir:index 969;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003022" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoplasia of the ulna" ]
  ], [
     fhir:index 970;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002205" ];
     fhir:CodeSystem.concept.display [ fhir:value "Recurrent respiratory infections" ]
  ], [
     fhir:index 971;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001669" ];
     fhir:CodeSystem.concept.display [ fhir:value "Transposition of the great arteries" ]
  ], [
     fhir:index 972;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001716" ];
     fhir:CodeSystem.concept.display [ fhir:value "Wolff-Parkinson-White syndrome" ]
  ], [
     fhir:index 973;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002758" ];
     fhir:CodeSystem.concept.display [ fhir:value "Osteoarthritis" ]
  ], [
     fhir:index 974;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002037" ];
     fhir:CodeSystem.concept.display [ fhir:value "Inflammation of the large intestine" ]
  ], [
     fhir:index 975;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009892" ];
     fhir:CodeSystem.concept.display [ fhir:value "Anotia" ]
  ], [
     fhir:index 976;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011331" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hemifacial atrophy" ]
  ], [
     fhir:index 977;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009118" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aplasia/Hypoplasia of the mandible" ]
  ], [
     fhir:index 978;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009940" ];
     fhir:CodeSystem.concept.display [ fhir:value "Asymmetry of the mandible" ]
  ], [
     fhir:index 979;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000682" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of dental enamel" ]
  ], [
     fhir:index 980;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009908" ];
     fhir:CodeSystem.concept.display [ fhir:value "Anterior creases of earlobe" ]
  ], [
     fhir:index 981;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001541" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ascites" ]
  ], [
     fhir:index 982;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006687" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aortic tortuosity" ]
  ], [
     fhir:index 983;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010535" ];
     fhir:CodeSystem.concept.display [ fhir:value "Sleep apnea" ]
  ], [
     fhir:index 984;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100633" ];
     fhir:CodeSystem.concept.display [ fhir:value "Esophagitis" ]
  ], [
     fhir:index 985;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002105" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hemoptysis" ]
  ], [
     fhir:index 986;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002613" ];
     fhir:CodeSystem.concept.display [ fhir:value "Biliary cirrhosis" ]
  ], [
     fhir:index 987;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004469" ];
     fhir:CodeSystem.concept.display [ fhir:value "Chronic bronchitis" ]
  ], [
     fhir:index 988;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002720" ];
     fhir:CodeSystem.concept.display [ fhir:value "Decreased circulating IgA level" ]
  ], [
     fhir:index 989;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002904" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyperbilirubinemia" ]
  ], [
     fhir:index 990;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003237" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased circulating IgG level" ]
  ], [
     fhir:index 991;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003262" ];
     fhir:CodeSystem.concept.display [ fhir:value "Smooth muscle antibody positivity" ]
  ], [
     fhir:index 992;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011227" ];
     fhir:CodeSystem.concept.display [ fhir:value "Elevated C-reactive protein level" ]
  ], [
     fhir:index 993;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001852" ];
     fhir:CodeSystem.concept.display [ fhir:value "Sandal gap" ]
  ], [
     fhir:index 994;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004381" ];
     fhir:CodeSystem.concept.display [ fhir:value "Supravalvular aortic stenosis" ]
  ], [
     fhir:index 995;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100700" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal arachnoid mater morphology" ]
  ], [
     fhir:index 996;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002624" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal venous morphology" ]
  ], [
     fhir:index 997;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002289" ];
     fhir:CodeSystem.concept.display [ fhir:value "Alopecia universalis" ]
  ], [
     fhir:index 998;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009588" ];
     fhir:CodeSystem.concept.display [ fhir:value "Vestibular Schwannoma" ]
  ], [
     fhir:index 999;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001648" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cor pulmonale" ]
  ], [
     fhir:index 1000;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002091" ];
     fhir:CodeSystem.concept.display [ fhir:value "Restrictive ventilatory defect" ]
  ], [
     fhir:index 1001;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002092" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pulmonary arterial hypertension" ]
  ], [
     fhir:index 1002;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002113" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pulmonary infiltrates" ]
  ], [
     fhir:index 1003;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003138" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased blood urea nitrogen" ]
  ], [
     fhir:index 1004;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003259" ];
     fhir:CodeSystem.concept.display [ fhir:value "Elevated serum creatinine" ]
  ], [
     fhir:index 1005;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005180" ];
     fhir:CodeSystem.concept.display [ fhir:value "Tricuspid regurgitation" ]
  ], [
     fhir:index 1006;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012585" ];
     fhir:CodeSystem.concept.display [ fhir:value "Renal atrophy" ]
  ], [
     fhir:index 1007;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005133" ];
     fhir:CodeSystem.concept.display [ fhir:value "Right ventricular dilatation" ]
  ], [
     fhir:index 1008;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005575" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hemolytic-uremic syndrome" ]
  ], [
     fhir:index 1009;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001697" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal pericardium morphology" ]
  ], [
     fhir:index 1010;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012486" ];
     fhir:CodeSystem.concept.display [ fhir:value "Myelitis" ]
  ], [
     fhir:index 1011;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002385" ];
     fhir:CodeSystem.concept.display [ fhir:value "Paraparesis" ]
  ], [
     fhir:index 1012;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006706" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cystic liver disease" ]
  ], [
     fhir:index 1013;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010880" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased nuchal translucency" ]
  ], [
     fhir:index 1014;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000457" ];
     fhir:CodeSystem.concept.display [ fhir:value "Depressed nasal ridge" ]
  ], [
     fhir:index 1015;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002263" ];
     fhir:CodeSystem.concept.display [ fhir:value "Exaggerated cupid's bow" ]
  ], [
     fhir:index 1016;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002500" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the cerebral white matter" ]
  ], [
     fhir:index 1017;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002835" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aspiration" ]
  ], [
     fhir:index 1018;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000600" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the pharynx" ]
  ], [
     fhir:index 1019;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004327" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal vitreous humor morphology" ]
  ], [
     fhir:index 1020;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004378" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the anus" ]
  ], [
     fhir:index 1021;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012374" ];
     fhir:CodeSystem.concept.display [ fhir:value "obsolete Abnormal globe morphology" ]
  ], [
     fhir:index 1022;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100768" ];
     fhir:CodeSystem.concept.display [ fhir:value "Choriocarcinoma" ]
  ], [
     fhir:index 1023;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030991" ];
     fhir:CodeSystem.concept.display [ fhir:value "Sclerosing cholangitis" ]
  ], [
     fhir:index 1024;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006510" ];
     fhir:CodeSystem.concept.display [ fhir:value "Chronic pulmonary obstruction" ]
  ], [
     fhir:index 1025;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000710" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyperorality" ]
  ], [
     fhir:index 1026;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001270" ];
     fhir:CodeSystem.concept.display [ fhir:value "Motor delay" ]
  ], [
     fhir:index 1027;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001548" ];
     fhir:CodeSystem.concept.display [ fhir:value "Overgrowth" ]
  ], [
     fhir:index 1028;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002311" ];
     fhir:CodeSystem.concept.display [ fhir:value "Incoordination" ]
  ], [
     fhir:index 1029;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006288" ];
     fhir:CodeSystem.concept.display [ fhir:value "Advanced eruption of teeth" ]
  ], [
     fhir:index 1030;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006323" ];
     fhir:CodeSystem.concept.display [ fhir:value "Premature loss of primary teeth" ]
  ], [
     fhir:index 1031;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009890" ];
     fhir:CodeSystem.concept.display [ fhir:value "High anterior hairline" ]
  ], [
     fhir:index 1032;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100034" ];
     fhir:CodeSystem.concept.display [ fhir:value "Motor tics" ]
  ], [
     fhir:index 1033;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100035" ];
     fhir:CodeSystem.concept.display [ fhir:value "Phonic tics" ]
  ], [
     fhir:index 1034;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000348" ];
     fhir:CodeSystem.concept.display [ fhir:value "High forehead" ]
  ], [
     fhir:index 1035;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001520" ];
     fhir:CodeSystem.concept.display [ fhir:value "Large for gestational age" ]
  ], [
     fhir:index 1036;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001239" ];
     fhir:CodeSystem.concept.display [ fhir:value "Wrist flexion contracture" ]
  ], [
     fhir:index 1037;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007359" ];
     fhir:CodeSystem.concept.display [ fhir:value "Focal-onset seizure" ]
  ], [
     fhir:index 1038;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000430" ];
     fhir:CodeSystem.concept.display [ fhir:value "Underdeveloped nasal alae" ]
  ], [
     fhir:index 1039;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007400" ];
     fhir:CodeSystem.concept.display [ fhir:value "Irregular hyperpigmentation" ]
  ], [
     fhir:index 1040;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100495" ];
     fhir:CodeSystem.concept.display [ fhir:value "Mastocytosis" ]
  ], [
     fhir:index 1041;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012378" ];
     fhir:CodeSystem.concept.display [ fhir:value "Fatigue" ]
  ], [
     fhir:index 1042;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002046" ];
     fhir:CodeSystem.concept.display [ fhir:value "Heat intolerance" ]
  ], [
     fhir:index 1043;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003270" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abdominal distention" ]
  ], [
     fhir:index 1044;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002180" ];
     fhir:CodeSystem.concept.display [ fhir:value "Neurodegeneration" ]
  ], [
     fhir:index 1045;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003493" ];
     fhir:CodeSystem.concept.display [ fhir:value "Antinuclear antibody positivity" ]
  ], [
     fhir:index 1046;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030057" ];
     fhir:CodeSystem.concept.display [ fhir:value "Autoimmune antibody positivity" ]
  ], [
     fhir:index 1047;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006802" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal anterior horn cell morphology" ]
  ], [
     fhir:index 1048;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000064" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoplastic labia minora" ]
  ], [
     fhir:index 1049;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000338" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypomimic face" ]
  ], [
     fhir:index 1050;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001642" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pulmonic stenosis" ]
  ], [
     fhir:index 1051;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011344" ];
     fhir:CodeSystem.concept.display [ fhir:value "Severe global developmental delay" ]
  ], [
     fhir:index 1052;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0200007" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal size of the palpebral fissures" ]
  ], [
     fhir:index 1053;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004464" ];
     fhir:CodeSystem.concept.display [ fhir:value "Postauricular pit" ]
  ], [
     fhir:index 1054;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000130" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the uterus" ]
  ], [
     fhir:index 1055;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000137" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the ovary" ]
  ], [
     fhir:index 1056;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000142" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal vagina morphology" ]
  ], [
     fhir:index 1057;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000370" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the middle ear" ]
  ], [
     fhir:index 1058;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011787" ];
     fhir:CodeSystem.concept.display [ fhir:value "Central hypothyroidism" ]
  ], [
     fhir:index 1059;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000274" ];
     fhir:CodeSystem.concept.display [ fhir:value "Small face" ]
  ], [
     fhir:index 1060;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000446" ];
     fhir:CodeSystem.concept.display [ fhir:value "Narrow nasal bridge" ]
  ], [
     fhir:index 1061;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000622" ];
     fhir:CodeSystem.concept.display [ fhir:value "Blurred vision" ]
  ], [
     fhir:index 1062;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001245" ];
     fhir:CodeSystem.concept.display [ fhir:value "Small thenar eminence" ]
  ], [
     fhir:index 1063;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009601" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aplasia/Hypoplasia of the thumb" ]
  ], [
     fhir:index 1064;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011343" ];
     fhir:CodeSystem.concept.display [ fhir:value "Moderate global developmental delay" ]
  ], [
     fhir:index 1065;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000419" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the nasal septum" ]
  ], [
     fhir:index 1066;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000502" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal conjunctiva morphology" ]
  ], [
     fhir:index 1067;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000591" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal sclera morphology" ]
  ], [
     fhir:index 1068;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000615" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal pupil morphology" ]
  ], [
     fhir:index 1069;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001163" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the metacarpal bones" ]
  ], [
     fhir:index 1070;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001832" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal metatarsal morphology" ]
  ], [
     fhir:index 1071;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001850" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the tarsal bones" ]
  ], [
     fhir:index 1072;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010490" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the palmar creases" ]
  ], [
     fhir:index 1073;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010881" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the umbilical cord" ]
  ], [
     fhir:index 1074;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009113" ];
     fhir:CodeSystem.concept.display [ fhir:value "Diaphragmatic weakness" ]
  ], [
     fhir:index 1075;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011664" ];
     fhir:CodeSystem.concept.display [ fhir:value "Left ventricular noncompaction cardiomyopathy" ]
  ], [
     fhir:index 1076;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100240" ];
     fhir:CodeSystem.concept.display [ fhir:value "Synostosis of joints" ]
  ], [
     fhir:index 1077;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001838" ];
     fhir:CodeSystem.concept.display [ fhir:value "Rocker bottom foot" ]
  ], [
     fhir:index 1078;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003717" ];
     fhir:CodeSystem.concept.display [ fhir:value "Minimal subcutaneous fat" ]
  ], [
     fhir:index 1079;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001339" ];
     fhir:CodeSystem.concept.display [ fhir:value "Lissencephaly" ]
  ], [
     fhir:index 1080;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001591" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bell-shaped thorax" ]
  ], [
     fhir:index 1081;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002655" ];
     fhir:CodeSystem.concept.display [ fhir:value "Spondyloepiphyseal dysplasia" ]
  ], [
     fhir:index 1082;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002983" ];
     fhir:CodeSystem.concept.display [ fhir:value "Micromelia" ]
  ], [
     fhir:index 1083;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003016" ];
     fhir:CodeSystem.concept.display [ fhir:value "Metaphyseal widening" ]
  ], [
     fhir:index 1084;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009826" ];
     fhir:CodeSystem.concept.display [ fhir:value "Limb undergrowth" ]
  ], [
     fhir:index 1085;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004488" ];
     fhir:CodeSystem.concept.display [ fhir:value "Macrocephaly at birth" ]
  ], [
     fhir:index 1086;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001695" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cardiac arrest" ]
  ], [
     fhir:index 1087;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001712" ];
     fhir:CodeSystem.concept.display [ fhir:value "Left ventricular hypertrophy" ]
  ], [
     fhir:index 1088;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100775" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dural ectasia" ]
  ], [
     fhir:index 1089;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000846" ];
     fhir:CodeSystem.concept.display [ fhir:value "Adrenal insufficiency" ]
  ], [
     fhir:index 1090;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002925" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased thyroid-stimulating hormone level" ]
  ], [
     fhir:index 1091;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100646" ];
     fhir:CodeSystem.concept.display [ fhir:value "Thyroiditis" ]
  ], [
     fhir:index 1092;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000836" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyperthyroidism" ]
  ], [
     fhir:index 1093;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004414" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the pulmonary artery" ]
  ], [
     fhir:index 1094;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000465" ];
     fhir:CodeSystem.concept.display [ fhir:value "Webbed neck" ]
  ], [
     fhir:index 1095;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000723" ];
     fhir:CodeSystem.concept.display [ fhir:value "Restrictive behavior" ]
  ], [
     fhir:index 1096;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002253" ];
     fhir:CodeSystem.concept.display [ fhir:value "Colonic diverticula" ]
  ], [
     fhir:index 1097;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001310" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dysmetria" ]
  ], [
     fhir:index 1098;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000093" ];
     fhir:CodeSystem.concept.display [ fhir:value "Proteinuria" ]
  ], [
     fhir:index 1099;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002907" ];
     fhir:CodeSystem.concept.display [ fhir:value "Microscopic hematuria" ]
  ], [
     fhir:index 1100;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003073" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoalbuminemia" ]
  ], [
     fhir:index 1101;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004315" ];
     fhir:CodeSystem.concept.display [ fhir:value "Decreased circulating IgG level" ]
  ], [
     fhir:index 1102;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000795" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the urethra" ]
  ], [
     fhir:index 1103;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001015" ];
     fhir:CodeSystem.concept.display [ fhir:value "Prominent superficial veins" ]
  ], [
     fhir:index 1104;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004691" ];
     fhir:CodeSystem.concept.display [ fhir:value "2-3 toe syndactyly" ]
  ], [
     fhir:index 1105;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005328" ];
     fhir:CodeSystem.concept.display [ fhir:value "Progeroid facial appearance" ]
  ], [
     fhir:index 1106;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005487" ];
     fhir:CodeSystem.concept.display [ fhir:value "Prominent metopic ridge" ]
  ], [
     fhir:index 1107;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007552" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal subcutaneous fat tissue distribution" ]
  ], [
     fhir:index 1108;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100678" ];
     fhir:CodeSystem.concept.display [ fhir:value "Premature skin wrinkling" ]
  ], [
     fhir:index 1109;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0031137" ];
     fhir:CodeSystem.concept.display [ fhir:value "Storage in hepatocytes" ]
  ], [
     fhir:index 1110;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002521" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypsarrhythmia" ]
  ], [
     fhir:index 1111;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005390" ];
     fhir:CodeSystem.concept.display [ fhir:value "Recurrent opportunistic infections" ]
  ], [
     fhir:index 1112;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002716" ];
     fhir:CodeSystem.concept.display [ fhir:value "Lymphadenopathy" ]
  ], [
     fhir:index 1113;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005379" ];
     fhir:CodeSystem.concept.display [ fhir:value "obsolete Severe T lymphocytopenia" ]
  ], [
     fhir:index 1114;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004432" ];
     fhir:CodeSystem.concept.display [ fhir:value "Agammaglobulinemia" ]
  ], [
     fhir:index 1115;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006695" ];
     fhir:CodeSystem.concept.display [ fhir:value "Atrioventricular canal defect" ]
  ], [
     fhir:index 1116;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001733" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pancreatitis" ]
  ], [
     fhir:index 1117;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002350" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cerebellar cyst" ]
  ], [
     fhir:index 1118;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012110" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoplasia of the pons" ]
  ], [
     fhir:index 1119;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001948" ];
     fhir:CodeSystem.concept.display [ fhir:value "Alkalosis" ]
  ], [
     fhir:index 1120;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003113" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypochloremia" ]
  ], [
     fhir:index 1121;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003155" ];
     fhir:CodeSystem.concept.display [ fhir:value "Elevated alkaline phosphatase" ]
  ], [
     fhir:index 1122;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003542" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased serum pyruvate" ]
  ], [
     fhir:index 1123;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000421" ];
     fhir:CodeSystem.concept.display [ fhir:value "Epistaxis" ]
  ], [
     fhir:index 1124;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0200136" ];
     fhir:CodeSystem.concept.display [ fhir:value "Oral-pharyngeal dysphagia" ]
  ], [
     fhir:index 1125;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000805" ];
     fhir:CodeSystem.concept.display [ fhir:value "Enuresis" ]
  ], [
     fhir:index 1126;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005616" ];
     fhir:CodeSystem.concept.display [ fhir:value "Accelerated skeletal maturation" ]
  ], [
     fhir:index 1127;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002459" ];
     fhir:CodeSystem.concept.display [ fhir:value "obsolete Dysautonomia" ]
  ], [
     fhir:index 1128;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007302" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bipolar affective disorder" ]
  ], [
     fhir:index 1129;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100602" ];
     fhir:CodeSystem.concept.display [ fhir:value "Preeclampsia" ]
  ], [
     fhir:index 1130;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100508" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of vitamin metabolism" ]
  ], [
     fhir:index 1131;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001140" ];
     fhir:CodeSystem.concept.display [ fhir:value "Limbal dermoid" ]
  ], [
     fhir:index 1132;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000143" ];
     fhir:CodeSystem.concept.display [ fhir:value "Rectovaginal fistula" ]
  ], [
     fhir:index 1133;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001746" ];
     fhir:CodeSystem.concept.display [ fhir:value "Asplenia" ]
  ], [
     fhir:index 1134;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012715" ];
     fhir:CodeSystem.concept.display [ fhir:value "Profound hearing impairment" ]
  ], [
     fhir:index 1135;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001748" ];
     fhir:CodeSystem.concept.display [ fhir:value "Polysplenia" ]
  ], [
     fhir:index 1136;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003072" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypercalcemia" ]
  ], [
     fhir:index 1137;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002905" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyperphosphatemia" ]
  ], [
     fhir:index 1138;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002901" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypocalcemia" ]
  ], [
     fhir:index 1139;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001367" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal joint morphology" ]
  ], [
     fhir:index 1140;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010562" ];
     fhir:CodeSystem.concept.display [ fhir:value "Keloids" ]
  ], [
     fhir:index 1141;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004430" ];
     fhir:CodeSystem.concept.display [ fhir:value "Severe combined immunodeficiency" ]
  ], [
     fhir:index 1142;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000003" ];
     fhir:CodeSystem.concept.display [ fhir:value "Multicystic kidney dysplasia" ]
  ], [
     fhir:index 1143;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010980" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyperlipoproteinemia" ]
  ], [
     fhir:index 1144;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002155" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypertriglyceridemia" ]
  ], [
     fhir:index 1145;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000520" ];
     fhir:CodeSystem.concept.display [ fhir:value "Proptosis" ]
  ], [
     fhir:index 1146;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000180" ];
     fhir:CodeSystem.concept.display [ fhir:value "Lobulated tongue" ]
  ], [
     fhir:index 1147;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005486" ];
     fhir:CodeSystem.concept.display [ fhir:value "Small fontanelle" ]
  ], [
     fhir:index 1148;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000891" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cervical ribs" ]
  ], [
     fhir:index 1149;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002557" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoplastic nipples" ]
  ], [
     fhir:index 1150;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009112" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aplasia of the left hemidiaphragm" ]
  ], [
     fhir:index 1151;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001719" ];
     fhir:CodeSystem.concept.display [ fhir:value "Double outlet right ventricle" ]
  ], [
     fhir:index 1152;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001682" ];
     fhir:CodeSystem.concept.display [ fhir:value "Subvalvular aortic stenosis" ]
  ], [
     fhir:index 1153;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001667" ];
     fhir:CodeSystem.concept.display [ fhir:value "Right ventricular hypertrophy" ]
  ], [
     fhir:index 1154;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002101" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal lung lobation" ]
  ], [
     fhir:index 1155;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002202" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pleural effusion" ]
  ], [
     fhir:index 1156;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002566" ];
     fhir:CodeSystem.concept.display [ fhir:value "Intestinal malrotation" ]
  ], [
     fhir:index 1157;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004510" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pancreatic islet-cell hyperplasia" ]
  ], [
     fhir:index 1158;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001747" ];
     fhir:CodeSystem.concept.display [ fhir:value "Accessory spleen" ]
  ], [
     fhir:index 1159;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002181" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cerebral edema" ]
  ], [
     fhir:index 1160;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000967" ];
     fhir:CodeSystem.concept.display [ fhir:value "Petechiae" ]
  ], [
     fhir:index 1161;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009702" ];
     fhir:CodeSystem.concept.display [ fhir:value "Carpal synostosis" ]
  ], [
     fhir:index 1162;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000927" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of skeletal maturation" ]
  ], [
     fhir:index 1163;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004348" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of bone mineral density" ]
  ], [
     fhir:index 1164;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003019" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the wrist" ]
  ], [
     fhir:index 1165;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003063" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the humerus" ]
  ], [
     fhir:index 1166;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001059" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pterygium" ]
  ], [
     fhir:index 1167;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001528" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hemihypertrophy" ]
  ], [
     fhir:index 1168;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011228" ];
     fhir:CodeSystem.concept.display [ fhir:value "Horizontal eyebrow" ]
  ], [
     fhir:index 1169;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000766" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the sternum" ]
  ], [
     fhir:index 1170;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001254" ];
     fhir:CodeSystem.concept.display [ fhir:value "Lethargy" ]
  ], [
     fhir:index 1171;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002360" ];
     fhir:CodeSystem.concept.display [ fhir:value "Sleep disturbance" ]
  ], [
     fhir:index 1172;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001063" ];
     fhir:CodeSystem.concept.display [ fhir:value "Acrocyanosis" ]
  ], [
     fhir:index 1173;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001769" ];
     fhir:CodeSystem.concept.display [ fhir:value "Broad foot" ]
  ], [
     fhir:index 1174;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010280" ];
     fhir:CodeSystem.concept.display [ fhir:value "Stomatitis" ]
  ], [
     fhir:index 1175;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001288" ];
     fhir:CodeSystem.concept.display [ fhir:value "Gait disturbance" ]
  ], [
     fhir:index 1176;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008330" ];
     fhir:CodeSystem.concept.display [ fhir:value "Reduced von Willebrand factor activity" ]
  ], [
     fhir:index 1177;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001954" ];
     fhir:CodeSystem.concept.display [ fhir:value "Recurrent fever" ]
  ], [
     fhir:index 1178;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004311" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal macrophage morphology" ]
  ], [
     fhir:index 1179;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012539" ];
     fhir:CodeSystem.concept.display [ fhir:value "Non-Hodgkin lymphoma" ]
  ], [
     fhir:index 1180;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002074" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased neuronal autofluorescent lipopigment" ]
  ], [
     fhir:index 1181;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002973" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the forearm" ]
  ], [
     fhir:index 1182;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003203" ];
     fhir:CodeSystem.concept.display [ fhir:value "Impaired oxidative burst" ]
  ], [
     fhir:index 1183;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003027" ];
     fhir:CodeSystem.concept.display [ fhir:value "Mesomelia" ]
  ], [
     fhir:index 1184;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002754" ];
     fhir:CodeSystem.concept.display [ fhir:value "Osteomyelitis" ]
  ], [
     fhir:index 1185;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004431" ];
     fhir:CodeSystem.concept.display [ fhir:value "Complement deficiency" ]
  ], [
     fhir:index 1186;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001258" ];
     fhir:CodeSystem.concept.display [ fhir:value "Spastic paraplegia" ]
  ], [
     fhir:index 1187;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012811" ];
     fhir:CodeSystem.concept.display [ fhir:value "Wide nasal ridge" ]
  ], [
     fhir:index 1188;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011832" ];
     fhir:CodeSystem.concept.display [ fhir:value "Narrow nasal tip" ]
  ], [
     fhir:index 1189;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000288" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the philtrum" ]
  ], [
     fhir:index 1190;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002357" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dysphasia" ]
  ], [
     fhir:index 1191;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000871" ];
     fhir:CodeSystem.concept.display [ fhir:value "Panhypopituitarism" ]
  ], [
     fhir:index 1192;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000233" ];
     fhir:CodeSystem.concept.display [ fhir:value "Thin vermilion border" ]
  ], [
     fhir:index 1193;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003281" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased serum ferritin" ]
  ], [
     fhir:index 1194;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010752" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cleft mandible" ]
  ], [
     fhir:index 1195;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000437" ];
     fhir:CodeSystem.concept.display [ fhir:value "Depressed nasal tip" ]
  ], [
     fhir:index 1196;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000453" ];
     fhir:CodeSystem.concept.display [ fhir:value "Choanal atresia" ]
  ], [
     fhir:index 1197;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000863" ];
     fhir:CodeSystem.concept.display [ fhir:value "Central diabetes insipidus" ]
  ], [
     fhir:index 1198;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000058" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the labia" ]
  ], [
     fhir:index 1199;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007418" ];
     fhir:CodeSystem.concept.display [ fhir:value "Alopecia totalis" ]
  ], [
     fhir:index 1200;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100765" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the tonsils" ]
  ], [
     fhir:index 1201;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100747" ];
     fhir:CodeSystem.concept.display [ fhir:value "Macrodactyly of toe" ]
  ], [
     fhir:index 1202;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002109" ];
     fhir:CodeSystem.concept.display [ fhir:value "obsolete Abnormality of the bronchi" ]
  ], [
     fhir:index 1203;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011950" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bronchiolitis" ]
  ], [
     fhir:index 1204;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002850" ];
     fhir:CodeSystem.concept.display [ fhir:value "Decreased circulating total IgM" ]
  ], [
     fhir:index 1205;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001395" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hepatic fibrosis" ]
  ], [
     fhir:index 1206;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010701" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal immunoglobulin level" ]
  ], [
     fhir:index 1207;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009928" ];
     fhir:CodeSystem.concept.display [ fhir:value "Thick nasal alae" ]
  ], [
     fhir:index 1208;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010807" ];
     fhir:CodeSystem.concept.display [ fhir:value "Open bite" ]
  ], [
     fhir:index 1209;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002126" ];
     fhir:CodeSystem.concept.display [ fhir:value "Polymicrogyria" ]
  ], [
     fhir:index 1210;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002900" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypokalemia" ]
  ], [
     fhir:index 1211;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000155" ];
     fhir:CodeSystem.concept.display [ fhir:value "Oral ulcer" ]
  ], [
     fhir:index 1212;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000135" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypogonadism" ]
  ], [
     fhir:index 1213;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100783" ];
     fhir:CodeSystem.concept.display [ fhir:value "Breast aplasia" ]
  ], [
     fhir:index 1214;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000336" ];
     fhir:CodeSystem.concept.display [ fhir:value "Prominent supraorbital ridges" ]
  ], [
     fhir:index 1215;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010557" ];
     fhir:CodeSystem.concept.display [ fhir:value "Overlapping fingers" ]
  ], [
     fhir:index 1216;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005100" ];
     fhir:CodeSystem.concept.display [ fhir:value "Premature birth following premature rupture of fetal membranes" ]
  ], [
     fhir:index 1217;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002594" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pancreatic hypoplasia" ]
  ], [
     fhir:index 1218;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010109" ];
     fhir:CodeSystem.concept.display [ fhir:value "Short hallux" ]
  ], [
     fhir:index 1219;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002334" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the cerebellar vermis" ]
  ], [
     fhir:index 1220;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003326" ];
     fhir:CodeSystem.concept.display [ fhir:value "Myalgia" ]
  ], [
     fhir:index 1221;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001645" ];
     fhir:CodeSystem.concept.display [ fhir:value "Sudden cardiac death" ]
  ], [
     fhir:index 1222;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001612" ];
     fhir:CodeSystem.concept.display [ fhir:value "Weak cry" ]
  ], [
     fhir:index 1223;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001618" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dysphonia" ]
  ], [
     fhir:index 1224;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001336" ];
     fhir:CodeSystem.concept.display [ fhir:value "Myoclonus" ]
  ], [
     fhir:index 1225;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001283" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bulbar palsy" ]
  ], [
     fhir:index 1226;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002080" ];
     fhir:CodeSystem.concept.display [ fhir:value "Intention tremor" ]
  ], [
     fhir:index 1227;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002174" ];
     fhir:CodeSystem.concept.display [ fhir:value "Postural tremor" ]
  ], [
     fhir:index 1228;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002064" ];
     fhir:CodeSystem.concept.display [ fhir:value "Spastic gait" ]
  ], [
     fhir:index 1229;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009800" ];
     fhir:CodeSystem.concept.display [ fhir:value "Maternal diabetes" ]
  ], [
     fhir:index 1230;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001662" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bradycardia" ]
  ], [
     fhir:index 1231;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006595" ];
     fhir:CodeSystem.concept.display [ fhir:value "Scapulohumeral synostosis" ]
  ], [
     fhir:index 1232;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005815" ];
     fhir:CodeSystem.concept.display [ fhir:value "Supernumerary ribs" ]
  ], [
     fhir:index 1233;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000307" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pointed chin" ]
  ], [
     fhir:index 1234;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012371" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyperplasia of midface" ]
  ], [
     fhir:index 1235;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002643" ];
     fhir:CodeSystem.concept.display [ fhir:value "Neonatal respiratory distress" ]
  ], [
     fhir:index 1236;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002093" ];
     fhir:CodeSystem.concept.display [ fhir:value "Respiratory insufficiency" ]
  ], [
     fhir:index 1237;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010310" ];
     fhir:CodeSystem.concept.display [ fhir:value "Chylothorax" ]
  ], [
     fhir:index 1238;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006376" ];
     fhir:CodeSystem.concept.display [ fhir:value "Limited elbow flexion" ]
  ], [
     fhir:index 1239;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006467" ];
     fhir:CodeSystem.concept.display [ fhir:value "Limited shoulder movement" ]
  ], [
     fhir:index 1240;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010505" ];
     fhir:CodeSystem.concept.display [ fhir:value "Limitation of movement at ankles" ]
  ], [
     fhir:index 1241;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010501" ];
     fhir:CodeSystem.concept.display [ fhir:value "Limitation of knee mobility" ]
  ], [
     fhir:index 1242;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009896" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the antitragus" ]
  ], [
     fhir:index 1243;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004404" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal nipple morphology" ]
  ], [
     fhir:index 1244;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011957" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal pectoral muscle morphology" ]
  ], [
     fhir:index 1245;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000777" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the thymus" ]
  ], [
     fhir:index 1246;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000418" ];
     fhir:CodeSystem.concept.display [ fhir:value "Narrow nasal ridge" ]
  ], [
     fhir:index 1247;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001572" ];
     fhir:CodeSystem.concept.display [ fhir:value "Macrodontia" ]
  ], [
     fhir:index 1248;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002967" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cubitus valgus" ]
  ], [
     fhir:index 1249;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000988" ];
     fhir:CodeSystem.concept.display [ fhir:value "Skin rash" ]
  ], [
     fhir:index 1250;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009733" ];
     fhir:CodeSystem.concept.display [ fhir:value "Glioma" ]
  ], [
     fhir:index 1251;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012452" ];
     fhir:CodeSystem.concept.display [ fhir:value "Restless legs" ]
  ], [
     fhir:index 1252;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100031" ];
     fhir:CodeSystem.concept.display [ fhir:value "Neoplasm of the thyroid gland" ]
  ], [
     fhir:index 1253;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030127" ];
     fhir:CodeSystem.concept.display [ fhir:value "Endometriosis" ]
  ], [
     fhir:index 1254;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000123" ];
     fhir:CodeSystem.concept.display [ fhir:value "Nephritis" ]
  ], [
     fhir:index 1255;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001974" ];
     fhir:CodeSystem.concept.display [ fhir:value "Leukocytosis" ]
  ], [
     fhir:index 1256;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010976" ];
     fhir:CodeSystem.concept.display [ fhir:value "B lymphocytopenia" ]
  ], [
     fhir:index 1257;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000010" ];
     fhir:CodeSystem.concept.display [ fhir:value "Recurrent urinary tract infections" ]
  ], [
     fhir:index 1258;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100807" ];
     fhir:CodeSystem.concept.display [ fhir:value "Long fingers" ]
  ], [
     fhir:index 1259;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000653" ];
     fhir:CodeSystem.concept.display [ fhir:value "Sparse eyelashes" ]
  ], [
     fhir:index 1260;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000171" ];
     fhir:CodeSystem.concept.display [ fhir:value "Microglossia" ]
  ], [
     fhir:index 1261;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002575" ];
     fhir:CodeSystem.concept.display [ fhir:value "Tracheoesophageal fistula" ]
  ], [
     fhir:index 1262;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009933" ];
     fhir:CodeSystem.concept.display [ fhir:value "Narrow naris" ]
  ], [
     fhir:index 1263;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000883" ];
     fhir:CodeSystem.concept.display [ fhir:value "Thin ribs" ]
  ], [
     fhir:index 1264;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000121" ];
     fhir:CodeSystem.concept.display [ fhir:value "Nephrocalcinosis" ]
  ], [
     fhir:index 1265;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001349" ];
     fhir:CodeSystem.concept.display [ fhir:value "Facial diplegia" ]
  ], [
     fhir:index 1266;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012037" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pectoralis amyotrophy" ]
  ], [
     fhir:index 1267;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100560" ];
     fhir:CodeSystem.concept.display [ fhir:value "Upper limb asymmetry" ]
  ], [
     fhir:index 1268;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005684" ];
     fhir:CodeSystem.concept.display [ fhir:value "Distal arthrogryposis" ]
  ], [
     fhir:index 1269;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010722" ];
     fhir:CodeSystem.concept.display [ fhir:value "Asymmetry of the ears" ]
  ], [
     fhir:index 1270;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009380" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aplasia of the fingers" ]
  ], [
     fhir:index 1271;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001657" ];
     fhir:CodeSystem.concept.display [ fhir:value "Prolonged QT interval" ]
  ], [
     fhir:index 1272;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002040" ];
     fhir:CodeSystem.concept.display [ fhir:value "Esophageal varix" ]
  ], [
     fhir:index 1273;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000613" ];
     fhir:CodeSystem.concept.display [ fhir:value "Photophobia" ]
  ], [
     fhir:index 1274;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000561" ];
     fhir:CodeSystem.concept.display [ fhir:value "Absent eyelashes" ]
  ], [
     fhir:index 1275;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002223" ];
     fhir:CodeSystem.concept.display [ fhir:value "Absent eyebrow" ]
  ], [
     fhir:index 1276;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002591" ];
     fhir:CodeSystem.concept.display [ fhir:value "Polyphagia" ]
  ], [
     fhir:index 1277;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002373" ];
     fhir:CodeSystem.concept.display [ fhir:value "Febrile seizure (within the age range of 3 months to 6 years)" ]
  ], [
     fhir:index 1278;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002419" ];
     fhir:CodeSystem.concept.display [ fhir:value "Molar tooth sign on MRI" ]
  ], [
     fhir:index 1279;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001010" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypopigmentation of the skin" ]
  ], [
     fhir:index 1280;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005772" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aplasia/Hypoplasia of the tibia" ]
  ], [
     fhir:index 1281;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002211" ];
     fhir:CodeSystem.concept.display [ fhir:value "White forelock" ]
  ], [
     fhir:index 1282;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007126" ];
     fhir:CodeSystem.concept.display [ fhir:value "Proximal amyotrophy" ]
  ], [
     fhir:index 1283;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003798" ];
     fhir:CodeSystem.concept.display [ fhir:value "Nemaline bodies" ]
  ], [
     fhir:index 1284;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006533" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bronchodysplasia" ]
  ], [
     fhir:index 1285;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003391" ];
     fhir:CodeSystem.concept.display [ fhir:value "Gowers sign" ]
  ], [
     fhir:index 1286;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000771" ];
     fhir:CodeSystem.concept.display [ fhir:value "Gynecomastia" ]
  ], [
     fhir:index 1287;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100785" ];
     fhir:CodeSystem.concept.display [ fhir:value "Insomnia" ]
  ], [
     fhir:index 1288;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010529" ];
     fhir:CodeSystem.concept.display [ fhir:value "Echolalia" ]
  ], [
     fhir:index 1289;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000363" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of earlobe" ]
  ], [
     fhir:index 1290;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002612" ];
     fhir:CodeSystem.concept.display [ fhir:value "Congenital hepatic fibrosis" ]
  ], [
     fhir:index 1291;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006721" ];
     fhir:CodeSystem.concept.display [ fhir:value "Acute lymphoblastic leukemia" ]
  ], [
     fhir:index 1292;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001958" ];
     fhir:CodeSystem.concept.display [ fhir:value "Nonketotic hypoglycemia" ]
  ], [
     fhir:index 1293;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003457" ];
     fhir:CodeSystem.concept.display [ fhir:value "EMG abnormality" ]
  ], [
     fhir:index 1294;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010636" ];
     fhir:CodeSystem.concept.display [ fhir:value "Schizencephaly" ]
  ], [
     fhir:index 1295;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005266" ];
     fhir:CodeSystem.concept.display [ fhir:value "Intestinal polyp" ]
  ], [
     fhir:index 1296;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0200063" ];
     fhir:CodeSystem.concept.display [ fhir:value "Colorectal polyposis" ]
  ], [
     fhir:index 1297;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001762" ];
     fhir:CodeSystem.concept.display [ fhir:value "Talipes equinovarus" ]
  ], [
     fhir:index 1298;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000056" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the clitoris" ]
  ], [
     fhir:index 1299;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008655" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aplasia/Hypoplasia of the fallopian tube" ]
  ], [
     fhir:index 1300;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002072" ];
     fhir:CodeSystem.concept.display [ fhir:value "Chorea" ]
  ], [
     fhir:index 1301;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008734" ];
     fhir:CodeSystem.concept.display [ fhir:value "Decreased testicular size" ]
  ], [
     fhir:index 1302;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002136" ];
     fhir:CodeSystem.concept.display [ fhir:value "Broad-based gait" ]
  ], [
     fhir:index 1303;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010958" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bilateral renal agenesis" ]
  ], [
     fhir:index 1304;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002510" ];
     fhir:CodeSystem.concept.display [ fhir:value "Spastic tetraplegia" ]
  ], [
     fhir:index 1305;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003234" ];
     fhir:CodeSystem.concept.display [ fhir:value "Decreased plasma carnitine" ]
  ], [
     fhir:index 1306;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000720" ];
     fhir:CodeSystem.concept.display [ fhir:value "Mood swings" ]
  ], [
     fhir:index 1307;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012638" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal nervous system physiology" ]
  ], [
     fhir:index 1308;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002803" ];
     fhir:CodeSystem.concept.display [ fhir:value "Congenital contracture" ]
  ], [
     fhir:index 1309;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000152" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of head or neck" ]
  ], [
     fhir:index 1310;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004377" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hematological neoplasm" ]
  ], [
     fhir:index 1311;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100006" ];
     fhir:CodeSystem.concept.display [ fhir:value "Neoplasm of the central nervous system" ]
  ], [
     fhir:index 1312;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012759" ];
     fhir:CodeSystem.concept.display [ fhir:value "Neurodevelopmental abnormality" ]
  ], [
     fhir:index 1313;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011805" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal skeletal muscle morphology" ]
  ], [
     fhir:index 1314;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003634" ];
     fhir:CodeSystem.concept.display [ fhir:value "Amyoplasia" ]
  ], [
     fhir:index 1315;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001507" ];
     fhir:CodeSystem.concept.display [ fhir:value "Growth abnormality" ]
  ], [
     fhir:index 1316;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001939" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of metabolism/homeostasis" ]
  ], [
     fhir:index 1317;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011013" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal circulating carbohydrate concentration" ]
  ], [
     fhir:index 1318;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0410008" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the peripheral nervous system" ]
  ], [
     fhir:index 1319;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0200134" ];
     fhir:CodeSystem.concept.display [ fhir:value "Epileptic encephalopathy" ]
  ], [
     fhir:index 1320;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001881" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal leukocyte morphology" ]
  ], [
     fhir:index 1321;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005549" ];
     fhir:CodeSystem.concept.display [ fhir:value "obsolete Congenital neutropenia" ]
  ], [
     fhir:index 1322;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004439" ];
     fhir:CodeSystem.concept.display [ fhir:value "Craniofacial dysostosis" ]
  ], [
     fhir:index 1323;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012443" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of brain morphology" ]
  ], [
     fhir:index 1324;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000202" ];
     fhir:CodeSystem.concept.display [ fhir:value "Oral cleft" ]
  ], [
     fhir:index 1325;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011842" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of skeletal morphology" ]
  ], [
     fhir:index 1326;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003808" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal muscle tone" ]
  ], [
     fhir:index 1327;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001574" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the integument" ]
  ], [
     fhir:index 1328;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030056" ];
     fhir:CodeSystem.concept.display [ fhir:value "Uncombable hair" ]
  ], [
     fhir:index 1329;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003549" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of connective tissue" ]
  ], [
     fhir:index 1330;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030875" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of pulmonary circulation" ]
  ], [
     fhir:index 1331;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000118" ];
     fhir:CodeSystem.concept.display [ fhir:value "Phenotypic abnormality" ]
  ], [
     fhir:index 1332;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012469" ];
     fhir:CodeSystem.concept.display [ fhir:value "Infantile spasms" ]
  ], [
     fhir:index 1333;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0032894" ];
     fhir:CodeSystem.concept.display [ fhir:value "Seizure precipitated by febrile infection" ]
  ], [
     fhir:index 1334;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100661" ];
     fhir:CodeSystem.concept.display [ fhir:value "Trigeminal neuralgia" ]
  ], [
     fhir:index 1335;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012207" ];
     fhir:CodeSystem.concept.display [ fhir:value "Reduced sperm motility" ]
  ], [
     fhir:index 1336;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000798" ];
     fhir:CodeSystem.concept.display [ fhir:value "Oligospermia" ]
  ], [
     fhir:index 1337;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012864" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal sperm morphology" ]
  ], [
     fhir:index 1338;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008232" ];
     fhir:CodeSystem.concept.display [ fhir:value "Elevated circulating follicle stimulating hormone level" ]
  ], [
     fhir:index 1339;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0040306" ];
     fhir:CodeSystem.concept.display [ fhir:value "Decreased male libido" ]
  ], [
     fhir:index 1340;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012208" ];
     fhir:CodeSystem.concept.display [ fhir:value "Immotile sperm" ]
  ], [
     fhir:index 1341;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000027" ];
     fhir:CodeSystem.concept.display [ fhir:value "Azoospermia" ]
  ], [
     fhir:index 1342;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000870" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased circulating prolactin concentration" ]
  ], [
     fhir:index 1343;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008187" ];
     fhir:CodeSystem.concept.display [ fhir:value "Absence of secondary sex characteristics" ]
  ], [
     fhir:index 1344;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010469" ];
     fhir:CodeSystem.concept.display [ fhir:value "Absent testis" ]
  ], [
     fhir:index 1345;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011969" ];
     fhir:CodeSystem.concept.display [ fhir:value "Elevated circulating luteinizing hormone level" ]
  ], [
     fhir:index 1346;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0040171" ];
     fhir:CodeSystem.concept.display [ fhir:value "Decreased serum testosterone level" ]
  ], [
     fhir:index 1347;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003251" ];
     fhir:CodeSystem.concept.display [ fhir:value "Male infertility" ]
  ], [
     fhir:index 1348;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009804" ];
     fhir:CodeSystem.concept.display [ fhir:value "Reduced number of teeth" ]
  ], [
     fhir:index 1349;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000548" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cone/cone-rod dystrophy" ]
  ], [
     fhir:index 1350;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000546" ];
     fhir:CodeSystem.concept.display [ fhir:value "Retinal degeneration" ]
  ], [
     fhir:index 1351;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008002" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of macular pigmentation" ]
  ], [
     fhir:index 1352;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000608" ];
     fhir:CodeSystem.concept.display [ fhir:value "Macular degeneration" ]
  ], [
     fhir:index 1353;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030611" ];
     fhir:CodeSystem.concept.display [ fhir:value "Retinal pigment epithelial loss on macular OCT" ]
  ], [
     fhir:index 1354;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001135" ];
     fhir:CodeSystem.concept.display [ fhir:value "Chorioretinal dystrophy" ]
  ], [
     fhir:index 1355;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030468" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal multifocal electroretinogram" ]
  ], [
     fhir:index 1356;
     fhir:CodeSystem.concept.code [ fhir:value "HP:00030532" ];
     fhir:CodeSystem.concept.display [ fhir:value "Visual acuity test abnormality" ]
  ], [
     fhir:index 1357;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007401" ];
     fhir:CodeSystem.concept.display [ fhir:value "Macular atrophy" ]
  ], [
     fhir:index 1358;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030466" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal full-field electroretinogram" ]
  ], [
     fhir:index 1359;
     fhir:CodeSystem.concept.code [ fhir:value "HP:007737" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bone spicule pigmentation of the retina" ]
  ], [
     fhir:index 1360;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011342" ];
     fhir:CodeSystem.concept.display [ fhir:value "Mild global developmental delay" ]
  ], [
     fhir:index 1361;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030610" ];
     fhir:CodeSystem.concept.display [ fhir:value "Photoreceptor outer segment loss on macular OCT" ]
  ], [
     fhir:index 1362;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007722" ];
     fhir:CodeSystem.concept.display [ fhir:value "Retinal pigment epithelial atrophy" ]
  ], [
     fhir:index 1363;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030493" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of foveal pigmentation" ]
  ], [
     fhir:index 1364;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007843" ];
     fhir:CodeSystem.concept.display [ fhir:value "Attenuation of retinal blood vessels" ]
  ], [
     fhir:index 1365;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007754" ];
     fhir:CodeSystem.concept.display [ fhir:value "Macular dystrophy" ]
  ], [
     fhir:index 1366;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011509" ];
     fhir:CodeSystem.concept.display [ fhir:value "Macular hyperpigmentation" ]
  ], [
     fhir:index 1367;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008527" ];
     fhir:CodeSystem.concept.display [ fhir:value "Congenital sensorineural hearing impairment" ]
  ], [
     fhir:index 1368;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0200070" ];
     fhir:CodeSystem.concept.display [ fhir:value "Peripheral retinal atrophy" ]
  ], [
     fhir:index 1369;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007793" ];
     fhir:CodeSystem.concept.display [ fhir:value "Granular macular appearance" ]
  ], [
     fhir:index 1370;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007987" ];
     fhir:CodeSystem.concept.display [ fhir:value "Progressive visual field defects" ]
  ], [
     fhir:index 1371;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100817" ];
     fhir:CodeSystem.concept.display [ fhir:value "Renovascular hypertension" ]
  ], [
     fhir:index 1372;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007868" ];
     fhir:CodeSystem.concept.display [ fhir:value "obsolete Age-related macular degeneration" ]
  ], [
     fhir:index 1373;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030527" ];
     fhir:CodeSystem.concept.display [ fhir:value "Very severe constriction of peripheral visual field" ]
  ], [
     fhir:index 1374;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030551" ];
     fhir:CodeSystem.concept.display [ fhir:value "Visual acuity light perception with projection" ]
  ], [
     fhir:index 1375;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011505" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cystoid macular edema" ]
  ], [
     fhir:index 1376;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010442" ];
     fhir:CodeSystem.concept.display [ fhir:value "Polydactyly" ]
  ], [
     fhir:index 1377;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007642" ];
     fhir:CodeSystem.concept.display [ fhir:value "Congenital stationary night blindness" ]
  ], [
     fhir:index 1378;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009073" ];
     fhir:CodeSystem.concept.display [ fhir:value "Progressive proximal muscle weakness" ]
  ], [
     fhir:index 1379;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003741" ];
     fhir:CodeSystem.concept.display [ fhir:value "Congenital muscular dystrophy" ]
  ], [
     fhir:index 1380;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100299" ];
     fhir:CodeSystem.concept.display [ fhir:value "Muscle fiber inclusion bodies" ]
  ], [
     fhir:index 1381;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003540" ];
     fhir:CodeSystem.concept.display [ fhir:value "Impaired platelet aggregation" ]
  ], [
     fhir:index 1382;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010489" ];
     fhir:CodeSystem.concept.display [ fhir:value "Absent palmar crease" ]
  ], [
     fhir:index 1383;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009824" ];
     fhir:CodeSystem.concept.display [ fhir:value "Upper limb undergrowth" ]
  ], [
     fhir:index 1384;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002395" ];
     fhir:CodeSystem.concept.display [ fhir:value "Lower limb hyperreflexia" ]
  ], [
     fhir:index 1385;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001138" ];
     fhir:CodeSystem.concept.display [ fhir:value "Optic neuropathy" ]
  ], [
     fhir:index 1386;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007103" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypointensity of cerebral white matter on MRI" ]
  ], [
     fhir:index 1387;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003458" ];
     fhir:CodeSystem.concept.display [ fhir:value "EMG: myopathic abnormalities" ]
  ], [
     fhir:index 1388;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002987" ];
     fhir:CodeSystem.concept.display [ fhir:value "Elbow flexion contracture" ]
  ], [
     fhir:index 1389;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006466" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ankle flexion contracture" ]
  ], [
     fhir:index 1390;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008458" ];
     fhir:CodeSystem.concept.display [ fhir:value "Progressive congenital scoliosis" ]
  ], [
     fhir:index 1391;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000473" ];
     fhir:CodeSystem.concept.display [ fhir:value "Torticollis" ]
  ], [
     fhir:index 1392;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011800" ];
     fhir:CodeSystem.concept.display [ fhir:value "Midface retrusion" ]
  ], [
     fhir:index 1393;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000597" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ophthalmoparesis" ]
  ], [
     fhir:index 1394;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005853" ];
     fhir:CodeSystem.concept.display [ fhir:value "Congenital foot contraction deformities" ]
  ], [
     fhir:index 1395;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007002" ];
     fhir:CodeSystem.concept.display [ fhir:value "Motor axonal neuropathy" ]
  ], [
     fhir:index 1396;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003327" ];
     fhir:CodeSystem.concept.display [ fhir:value "Axial muscle weakness" ]
  ], [
     fhir:index 1397;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003306" ];
     fhir:CodeSystem.concept.display [ fhir:value "Spinal rigidity" ]
  ], [
     fhir:index 1398;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002068" ];
     fhir:CodeSystem.concept.display [ fhir:value "Neuromuscular dysphagia" ]
  ], [
     fhir:index 1399;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001002" ];
     fhir:CodeSystem.concept.display [ fhir:value "obsolete Decreased subcutaneous fat" ]
  ], [
     fhir:index 1400;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002880" ];
     fhir:CodeSystem.concept.display [ fhir:value "obsolete Respiratory difficulties" ]
  ], [
     fhir:index 1401;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006829" ];
     fhir:CodeSystem.concept.display [ fhir:value "Severe muscular hypotonia" ]
  ], [
     fhir:index 1402;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011448" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ankle clonus" ]
  ], [
     fhir:index 1403;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003487" ];
     fhir:CodeSystem.concept.display [ fhir:value "Babinski sign" ]
  ], [
     fhir:index 1404;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002378" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hand tremor" ]
  ], [
     fhir:index 1405;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002747" ];
     fhir:CodeSystem.concept.display [ fhir:value "Respiratory insufficiency due to muscle weakness" ]
  ], [
     fhir:index 1406;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002579" ];
     fhir:CodeSystem.concept.display [ fhir:value "Gastrointestinal dysmotility" ]
  ], [
     fhir:index 1407;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001041" ];
     fhir:CodeSystem.concept.display [ fhir:value "Facial erythema" ]
  ], [
     fhir:index 1408;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0040180" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyperkeratosis pilaris" ]
  ], [
     fhir:index 1409;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001382" ];
     fhir:CodeSystem.concept.display [ fhir:value "Joint hypermobility" ]
  ], [
     fhir:index 1410;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003722" ];
     fhir:CodeSystem.concept.display [ fhir:value "Neck flexor weakness" ]
  ], [
     fhir:index 1411;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003323" ];
     fhir:CodeSystem.concept.display [ fhir:value "Progressive muscle weakness" ]
  ], [
     fhir:index 1412;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002380" ];
     fhir:CodeSystem.concept.display [ fhir:value "Fasciculations" ]
  ], [
     fhir:index 1413;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012785" ];
     fhir:CodeSystem.concept.display [ fhir:value "Flexion contracture of finger" ]
  ], [
     fhir:index 1414;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007936" ];
     fhir:CodeSystem.concept.display [ fhir:value "Restrictive external ophthalmoplegia" ]
  ], [
     fhir:index 1415;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030319" ];
     fhir:CodeSystem.concept.display [ fhir:value "Weakness of facial musculature" ]
  ], [
     fhir:index 1416;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008936" ];
     fhir:CodeSystem.concept.display [ fhir:value "Muscular hypotonia of the trunk" ]
  ], [
     fhir:index 1417;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030230" ];
     fhir:CodeSystem.concept.display [ fhir:value "Central core regions in muscle fibers" ]
  ], [
     fhir:index 1418;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011471" ];
     fhir:CodeSystem.concept.display [ fhir:value "Gastrostomy tube feeding in infancy" ]
  ], [
     fhir:index 1419;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001290" ];
     fhir:CodeSystem.concept.display [ fhir:value "Generalized hypotonia" ]
  ], [
     fhir:index 1420;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002421" ];
     fhir:CodeSystem.concept.display [ fhir:value "Poor head control" ]
  ], [
     fhir:index 1421;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010301" ];
     fhir:CodeSystem.concept.display [ fhir:value "Spinal dysraphism" ]
  ], [
     fhir:index 1422;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004303" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal muscle fiber morphology" ]
  ], [
     fhir:index 1423;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009046" ];
     fhir:CodeSystem.concept.display [ fhir:value "Difficulty running" ]
  ], [
     fhir:index 1424;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003715" ];
     fhir:CodeSystem.concept.display [ fhir:value "Myofibrillar myopathy" ]
  ], [
     fhir:index 1425;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000467" ];
     fhir:CodeSystem.concept.display [ fhir:value "Neck muscle weakness" ]
  ], [
     fhir:index 1426;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001999" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal facial shape" ]
  ], [
     fhir:index 1427;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002751" ];
     fhir:CodeSystem.concept.display [ fhir:value "Kyphoscoliosis" ]
  ], [
     fhir:index 1428;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030223" ];
     fhir:CodeSystem.concept.display [ fhir:value "Perseveration" ]
  ], [
     fhir:index 1429;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002344" ];
     fhir:CodeSystem.concept.display [ fhir:value "Progressive neurologic deterioration" ]
  ], [
     fhir:index 1430;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002522" ];
     fhir:CodeSystem.concept.display [ fhir:value "Areflexia of lower limbs" ]
  ], [
     fhir:index 1431;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003805" ];
     fhir:CodeSystem.concept.display [ fhir:value "Rimmed vacuoles" ]
  ], [
     fhir:index 1432;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005781" ];
     fhir:CodeSystem.concept.display [ fhir:value "Contractures of the large joints" ]
  ], [
     fhir:index 1433;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0040083" ];
     fhir:CodeSystem.concept.display [ fhir:value "Toe walking" ]
  ], [
     fhir:index 1434;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003749" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pelvic girdle muscle weakness" ]
  ], [
     fhir:index 1435;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012444" ];
     fhir:CodeSystem.concept.display [ fhir:value "Brain atrophy" ]
  ], [
     fhir:index 1436;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003738" ];
     fhir:CodeSystem.concept.display [ fhir:value "Exercise-induced myalgia" ]
  ], [
     fhir:index 1437;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003756" ];
     fhir:CodeSystem.concept.display [ fhir:value "Skeletal myopathy" ]
  ], [
     fhir:index 1438;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002492" ];
     fhir:CodeSystem.concept.display [ fhir:value "Morphological abnormality of the corticospinal tract" ]
  ], [
     fhir:index 1439;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100302" ];
     fhir:CodeSystem.concept.display [ fhir:value "Muscle fiber tubuloreticular inclusions" ]
  ], [
     fhir:index 1440;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006817" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aplasia/Hypoplasia of the cerebellar vermis" ]
  ], [
     fhir:index 1441;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003473" ];
     fhir:CodeSystem.concept.display [ fhir:value "Fatigable weakness" ]
  ], [
     fhir:index 1442;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002077" ];
     fhir:CodeSystem.concept.display [ fhir:value "Migraine with aura" ]
  ], [
     fhir:index 1443;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100559" ];
     fhir:CodeSystem.concept.display [ fhir:value "Lower limb asymmetry" ]
  ], [
     fhir:index 1444;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002079" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoplasia of the corpus callosum" ]
  ], [
     fhir:index 1445;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002804" ];
     fhir:CodeSystem.concept.display [ fhir:value "Arthrogryposis multiplex congenita" ]
  ], [
     fhir:index 1446;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011623" ];
     fhir:CodeSystem.concept.display [ fhir:value "Muscular ventricular septal defect" ]
  ], [
     fhir:index 1447;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002191" ];
     fhir:CodeSystem.concept.display [ fhir:value "Progressive spasticity" ]
  ], [
     fhir:index 1448;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003390" ];
     fhir:CodeSystem.concept.display [ fhir:value "Sensory axonal neuropathy" ]
  ], [
     fhir:index 1449;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006986" ];
     fhir:CodeSystem.concept.display [ fhir:value "Upper limb spasticity" ]
  ], [
     fhir:index 1450;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002464" ];
     fhir:CodeSystem.concept.display [ fhir:value "Spastic dysarthria" ]
  ], [
     fhir:index 1451;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001308" ];
     fhir:CodeSystem.concept.display [ fhir:value "Tongue fasciculations" ]
  ], [
     fhir:index 1452;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007010" ];
     fhir:CodeSystem.concept.display [ fhir:value "Poor fine motor coordination" ]
  ], [
     fhir:index 1453;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003737" ];
     fhir:CodeSystem.concept.display [ fhir:value "Mitochondrial myopathy" ]
  ], [
     fhir:index 1454;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008012" ];
     fhir:CodeSystem.concept.display [ fhir:value "obsolete Congenital myopia" ]
  ], [
     fhir:index 1455;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008872" ];
     fhir:CodeSystem.concept.display [ fhir:value "Feeding difficulties in infancy" ]
  ], [
     fhir:index 1456;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005750" ];
     fhir:CodeSystem.concept.display [ fhir:value "Contractures of the joints of the lower limbs" ]
  ], [
     fhir:index 1457;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009067" ];
     fhir:CodeSystem.concept.display [ fhir:value "Progressive spinal muscular atrophy" ]
  ], [
     fhir:index 1458;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001623" ];
     fhir:CodeSystem.concept.display [ fhir:value "Breech presentation" ]
  ], [
     fhir:index 1459;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001374" ];
     fhir:CodeSystem.concept.display [ fhir:value "Congenital hip dislocation" ]
  ], [
     fhir:index 1460;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002359" ];
     fhir:CodeSystem.concept.display [ fhir:value "Frequent falls" ]
  ], [
     fhir:index 1461;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003803" ];
     fhir:CodeSystem.concept.display [ fhir:value "Type 1 muscle fiber predominance" ]
  ], [
     fhir:index 1462;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011410" ];
     fhir:CodeSystem.concept.display [ fhir:value "Caesarian section" ]
  ], [
     fhir:index 1463;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008947" ];
     fhir:CodeSystem.concept.display [ fhir:value "Infantile muscular hypotonia" ]
  ], [
     fhir:index 1464;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100501" ];
     fhir:CodeSystem.concept.display [ fhir:value "Recurrent bronchiolitis" ]
  ], [
     fhir:index 1465;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003789" ];
     fhir:CodeSystem.concept.display [ fhir:value "Minicore myopathy" ]
  ], [
     fhir:index 1466;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000544" ];
     fhir:CodeSystem.concept.display [ fhir:value "External ophthalmoplegia" ]
  ], [
     fhir:index 1467;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001605" ];
     fhir:CodeSystem.concept.display [ fhir:value "Vocal cord paralysis" ]
  ], [
     fhir:index 1468;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003712" ];
     fhir:CodeSystem.concept.display [ fhir:value "Skeletal muscle hypertrophy" ]
  ], [
     fhir:index 1469;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012507" ];
     fhir:CodeSystem.concept.display [ fhir:value "Weakness of orbicularis oculi muscle" ]
  ], [
     fhir:index 1470;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009816" ];
     fhir:CodeSystem.concept.display [ fhir:value "Lower limb undergrowth" ]
  ], [
     fhir:index 1471;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008935" ];
     fhir:CodeSystem.concept.display [ fhir:value "Generalized neonatal hypotonia" ]
  ], [
     fhir:index 1472;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003484" ];
     fhir:CodeSystem.concept.display [ fhir:value "Upper limb muscle weakness" ]
  ], [
     fhir:index 1473;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008331" ];
     fhir:CodeSystem.concept.display [ fhir:value "Elevated creatine kinase after exercise" ]
  ], [
     fhir:index 1474;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001315" ];
     fhir:CodeSystem.concept.display [ fhir:value "Reduced tendon reflexes" ]
  ], [
     fhir:index 1475;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012473" ];
     fhir:CodeSystem.concept.display [ fhir:value "Tongue atrophy" ]
  ], [
     fhir:index 1476;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003273" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hip contracture" ]
  ], [
     fhir:index 1477;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006380" ];
     fhir:CodeSystem.concept.display [ fhir:value "Knee flexion contracture" ]
  ], [
     fhir:index 1478;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003752" ];
     fhir:CodeSystem.concept.display [ fhir:value "Episodic flaccid weakness" ]
  ], [
     fhir:index 1479;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100298" ];
     fhir:CodeSystem.concept.display [ fhir:value "Motheaten muscle fibers" ]
  ], [
     fhir:index 1480;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003693" ];
     fhir:CodeSystem.concept.display [ fhir:value "Distal amyotrophy" ]
  ], [
     fhir:index 1481;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002167" ];
     fhir:CodeSystem.concept.display [ fhir:value "Neurological speech impairment" ]
  ], [
     fhir:index 1482;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003388" ];
     fhir:CodeSystem.concept.display [ fhir:value "Easy fatigability" ]
  ], [
     fhir:index 1483;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001348" ];
     fhir:CodeSystem.concept.display [ fhir:value "Brisk reflexes" ]
  ], [
     fhir:index 1484;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003445" ];
     fhir:CodeSystem.concept.display [ fhir:value "EMG: neuropathic changes" ]
  ], [
     fhir:index 1485;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009063" ];
     fhir:CodeSystem.concept.display [ fhir:value "Progressive distal muscle weakness" ]
  ], [
     fhir:index 1486;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003720" ];
     fhir:CodeSystem.concept.display [ fhir:value "Generalized muscle hypertrophy" ]
  ], [
     fhir:index 1487;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002493" ];
     fhir:CodeSystem.concept.display [ fhir:value "Upper motor neuron dysfunction" ]
  ], [
     fhir:index 1488;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012448" ];
     fhir:CodeSystem.concept.display [ fhir:value "Delayed myelination" ]
  ], [
     fhir:index 1489;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001338" ];
     fhir:CodeSystem.concept.display [ fhir:value "Partial agenesis of the corpus callosum" ]
  ], [
     fhir:index 1490;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006879" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pontocerebellar atrophy" ]
  ], [
     fhir:index 1491;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0200101" ];
     fhir:CodeSystem.concept.display [ fhir:value "Decreased/absent ankle reflexes" ]
  ], [
     fhir:index 1492;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009020" ];
     fhir:CodeSystem.concept.display [ fhir:value "Exercise-induced muscle fatigue" ]
  ], [
     fhir:index 1493;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002067" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bradykinesia" ]
  ], [
     fhir:index 1494;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012751" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal basal ganglia MRI signal intensity" ]
  ], [
     fhir:index 1495;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003355" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aminoaciduria" ]
  ], [
     fhir:index 1496;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012450" ];
     fhir:CodeSystem.concept.display [ fhir:value "Chronic constipation" ]
  ], [
     fhir:index 1497;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011834" ];
     fhir:CodeSystem.concept.display [ fhir:value "Moyamoya phenomenon" ]
  ], [
     fhir:index 1498;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001297" ];
     fhir:CodeSystem.concept.display [ fhir:value "Stroke" ]
  ], [
     fhir:index 1499;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0200049" ];
     fhir:CodeSystem.concept.display [ fhir:value "Upper limb hypertonia" ]
  ], [
     fhir:index 1500;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008981" ];
     fhir:CodeSystem.concept.display [ fhir:value "Calf muscle hypertrophy" ]
  ], [
     fhir:index 1501;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006785" ];
     fhir:CodeSystem.concept.display [ fhir:value "Limb-girdle muscular dystrophy" ]
  ], [
     fhir:index 1502;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006957" ];
     fhir:CodeSystem.concept.display [ fhir:value "Loss of ability to walk" ]
  ], [
     fhir:index 1503;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030098" ];
     fhir:CodeSystem.concept.display [ fhir:value "Reduced muscle dystrophin expression" ]
  ], [
     fhir:index 1504;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030115" ];
     fhir:CodeSystem.concept.display [ fhir:value "Reduced muscle fiber dysferlin" ]
  ], [
     fhir:index 1505;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002058" ];
     fhir:CodeSystem.concept.display [ fhir:value "Myopathic facies" ]
  ], [
     fhir:index 1506;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007858" ];
     fhir:CodeSystem.concept.display [ fhir:value "Chorioretinal lacunae" ]
  ], [
     fhir:index 1507;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006657" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoplasia of first ribs" ]
  ], [
     fhir:index 1508;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007165" ];
     fhir:CodeSystem.concept.display [ fhir:value "Periventricular heterotopia" ]
  ], [
     fhir:index 1509;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009779" ];
     fhir:CodeSystem.concept.display [ fhir:value "3-4 toe syndactyly" ]
  ], [
     fhir:index 1510;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010665" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bilateral coxa valga" ]
  ], [
     fhir:index 1511;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007598" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bilateral single transverse palmar creases" ]
  ], [
     fhir:index 1512;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006101" ];
     fhir:CodeSystem.concept.display [ fhir:value "Finger syndactyly" ]
  ], [
     fhir:index 1513;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010511" ];
     fhir:CodeSystem.concept.display [ fhir:value "Long toe" ]
  ], [
     fhir:index 1514;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002370" ];
     fhir:CodeSystem.concept.display [ fhir:value "Poor coordination" ]
  ], [
     fhir:index 1515;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000480" ];
     fhir:CodeSystem.concept.display [ fhir:value "Retinal coloboma" ]
  ], [
     fhir:index 1516;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001770" ];
     fhir:CodeSystem.concept.display [ fhir:value "Toe syndactyly" ]
  ], [
     fhir:index 1517;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010851" ];
     fhir:CodeSystem.concept.display [ fhir:value "EEG with burst suppression" ]
  ], [
     fhir:index 1518;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002791" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoventilation" ]
  ], [
     fhir:index 1519;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0040075" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypopituitarism" ]
  ], [
     fhir:index 1520;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012506" ];
     fhir:CodeSystem.concept.display [ fhir:value "Small pituitary gland" ]
  ], [
     fhir:index 1521;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000538" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pseudopapilledema" ]
  ], [
     fhir:index 1522;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012717" ];
     fhir:CodeSystem.concept.display [ fhir:value "Severe conductive hearing impairment" ]
  ], [
     fhir:index 1523;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001370" ];
     fhir:CodeSystem.concept.display [ fhir:value "Rheumatoid arthritis" ]
  ], [
     fhir:index 1524;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000016" ];
     fhir:CodeSystem.concept.display [ fhir:value "Urinary retention" ]
  ], [
     fhir:index 1525;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012537" ];
     fhir:CodeSystem.concept.display [ fhir:value "Food intolerance" ]
  ], [
     fhir:index 1526;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011297" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal digit morphology" ]
  ], [
     fhir:index 1527;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001273" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal corpus callosum morphology" ]
  ], [
     fhir:index 1528;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030148" ];
     fhir:CodeSystem.concept.display [ fhir:value "Heart murmur" ]
  ], [
     fhir:index 1529;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0045018" ];
     fhir:CodeSystem.concept.display [ fhir:value "Partial duplication of eyebrows" ]
  ], [
     fhir:index 1530;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008998" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pectoralis hypoplasia" ]
  ], [
     fhir:index 1531;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001707" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal right ventricle morphology" ]
  ], [
     fhir:index 1532;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001540" ];
     fhir:CodeSystem.concept.display [ fhir:value "Diastasis recti" ]
  ], [
     fhir:index 1533;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100693" ];
     fhir:CodeSystem.concept.display [ fhir:value "Iridodonesis" ]
  ], [
     fhir:index 1534;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002265" ];
     fhir:CodeSystem.concept.display [ fhir:value "Large fleshy ears" ]
  ], [
     fhir:index 1535;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001132" ];
     fhir:CodeSystem.concept.display [ fhir:value "Lens subluxation" ]
  ], [
     fhir:index 1536;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004927" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pulmonary artery dilatation" ]
  ], [
     fhir:index 1537;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005619" ];
     fhir:CodeSystem.concept.display [ fhir:value "Thoracolumbar kyphosis" ]
  ], [
     fhir:index 1538;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008619" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bilateral sensorineural hearing impairment" ]
  ], [
     fhir:index 1539;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001045" ];
     fhir:CodeSystem.concept.display [ fhir:value "Vitiligo" ]
  ], [
     fhir:index 1540;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009124" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal adipose tissue morphology" ]
  ], [
     fhir:index 1541;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002979" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bowing of the legs" ]
  ], [
     fhir:index 1542;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000455" ];
     fhir:CodeSystem.concept.display [ fhir:value "Broad nasal tip" ]
  ], [
     fhir:index 1543;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001007" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hirsutism" ]
  ], [
     fhir:index 1544;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010314" ];
     fhir:CodeSystem.concept.display [ fhir:value "Premature thelarche" ]
  ], [
     fhir:index 1545;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000075" ];
     fhir:CodeSystem.concept.display [ fhir:value "Renal duplication" ]
  ], [
     fhir:index 1546;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000368" ];
     fhir:CodeSystem.concept.display [ fhir:value "Low-set, posteriorly rotated ears" ]
  ], [
     fhir:index 1547;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001052" ];
     fhir:CodeSystem.concept.display [ fhir:value "Nevus flammeus" ]
  ], [
     fhir:index 1548;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0200048" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cyanotic episode" ]
  ], [
     fhir:index 1549;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001902" ];
     fhir:CodeSystem.concept.display [ fhir:value "Giant platelets" ]
  ], [
     fhir:index 1550;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030043" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hip subluxation" ]
  ], [
     fhir:index 1551;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002938" ];
     fhir:CodeSystem.concept.display [ fhir:value "Lumbar hyperlordosis" ]
  ], [
     fhir:index 1552;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030084" ];
     fhir:CodeSystem.concept.display [ fhir:value "Clinodactyly" ]
  ], [
     fhir:index 1553;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005560" ];
     fhir:CodeSystem.concept.display [ fhir:value "Imbalanced hemoglobin synthesis" ]
  ], [
     fhir:index 1554;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001539" ];
     fhir:CodeSystem.concept.display [ fhir:value "Omphalocele" ]
  ], [
     fhir:index 1555;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009778" ];
     fhir:CodeSystem.concept.display [ fhir:value "Short thumb" ]
  ], [
     fhir:index 1556;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002277" ];
     fhir:CodeSystem.concept.display [ fhir:value "Horner syndrome" ]
  ], [
     fhir:index 1557;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011701" ];
     fhir:CodeSystem.concept.display [ fhir:value "Multifocal atrial tachycardia" ]
  ], [
     fhir:index 1558;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005274" ];
     fhir:CodeSystem.concept.display [ fhir:value "Prominent nasal tip" ]
  ], [
     fhir:index 1559;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001262" ];
     fhir:CodeSystem.concept.display [ fhir:value "Excessive daytime somnolence" ]
  ], [
     fhir:index 1560;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001285" ];
     fhir:CodeSystem.concept.display [ fhir:value "Spastic tetraparesis" ]
  ], [
     fhir:index 1561;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012171" ];
     fhir:CodeSystem.concept.display [ fhir:value "Stereotypical hand wringing" ]
  ], [
     fhir:index 1562;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002518" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the periventricular white matter" ]
  ], [
     fhir:index 1563;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005692" ];
     fhir:CodeSystem.concept.display [ fhir:value "Joint hyperflexibility" ]
  ], [
     fhir:index 1564;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007440" ];
     fhir:CodeSystem.concept.display [ fhir:value "Generalized hyperpigmentation" ]
  ], [
     fhir:index 1565;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001805" ];
     fhir:CodeSystem.concept.display [ fhir:value "Onychogryposis" ]
  ], [
     fhir:index 1566;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011945" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bronchiolitis obliterans organizing pneumonia" ]
  ], [
     fhir:index 1567;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003763" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bruxism" ]
  ], [
     fhir:index 1568;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010500" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyperextensibility of the knee" ]
  ], [
     fhir:index 1569;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0040115" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the Eustachian tube" ]
  ], [
     fhir:index 1570;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008751" ];
     fhir:CodeSystem.concept.display [ fhir:value "Laryngeal cleft" ]
  ], [
     fhir:index 1571;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000403" ];
     fhir:CodeSystem.concept.display [ fhir:value "Recurrent otitis media" ]
  ], [
     fhir:index 1572;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001787" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal delivery" ]
  ], [
     fhir:index 1573;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002571" ];
     fhir:CodeSystem.concept.display [ fhir:value "Achalasia" ]
  ], [
     fhir:index 1574;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002615" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypotension" ]
  ], [
     fhir:index 1575;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003550" ];
     fhir:CodeSystem.concept.display [ fhir:value "Predominantly lower limb lymphedema" ]
  ], [
     fhir:index 1576;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030363" ];
     fhir:CodeSystem.concept.display [ fhir:value "Primary Caesarian section" ]
  ], [
     fhir:index 1577;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001727" ];
     fhir:CodeSystem.concept.display [ fhir:value "Thromboembolic stroke" ]
  ], [
     fhir:index 1578;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100603" ];
     fhir:CodeSystem.concept.display [ fhir:value "Toxemia of pregnancy" ]
  ], [
     fhir:index 1579;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010836" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal circulating copper concentration" ]
  ], [
     fhir:index 1580;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000356" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the outer ear" ]
  ], [
     fhir:index 1581;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002197" ];
     fhir:CodeSystem.concept.display [ fhir:value "Generalized-onset seizure" ]
  ], [
     fhir:index 1582;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011436" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal maternal serum screening" ]
  ], [
     fhir:index 1583;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003517" ];
     fhir:CodeSystem.concept.display [ fhir:value "Birth length greater than 97th percentile" ]
  ], [
     fhir:index 1584;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003561" ];
     fhir:CodeSystem.concept.display [ fhir:value "Birth length less than 3rd percentile" ]
  ], [
     fhir:index 1585;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012188" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyperemesis gravidarum" ]
  ], [
     fhir:index 1586;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010519" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased fetal movement" ]
  ], [
     fhir:index 1587;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030244" ];
     fhir:CodeSystem.concept.display [ fhir:value "Maternal fever in pregnancy" ]
  ], [
     fhir:index 1588;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008071" ];
     fhir:CodeSystem.concept.display [ fhir:value "Maternal hypertension" ]
  ], [
     fhir:index 1589;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100622" ];
     fhir:CodeSystem.concept.display [ fhir:value "Maternal seizure" ]
  ], [
     fhir:index 1590;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011438" ];
     fhir:CodeSystem.concept.display [ fhir:value "Maternal teratogenic exposure" ]
  ], [
     fhir:index 1591;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001998" ];
     fhir:CodeSystem.concept.display [ fhir:value "Neonatal hypoglycemia" ]
  ], [
     fhir:index 1592;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0040187" ];
     fhir:CodeSystem.concept.display [ fhir:value "Neonatal sepsis" ]
  ], [
     fhir:index 1593;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002033" ];
     fhir:CodeSystem.concept.display [ fhir:value "Poor suck" ]
  ], [
     fhir:index 1594;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006579" ];
     fhir:CodeSystem.concept.display [ fhir:value "Prolonged neonatal jaundice" ]
  ], [
     fhir:index 1595;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001724" ];
     fhir:CodeSystem.concept.display [ fhir:value "obsolete Aortic dilatation" ]
  ], [
     fhir:index 1596;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010621" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cutaneous syndactyly of toes" ]
  ], [
     fhir:index 1597;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001880" ];
     fhir:CodeSystem.concept.display [ fhir:value "Eosinophilia" ]
  ], [
     fhir:index 1598;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000162" ];
     fhir:CodeSystem.concept.display [ fhir:value "Glossoptosis" ]
  ], [
     fhir:index 1599;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100578" ];
     fhir:CodeSystem.concept.display [ fhir:value "Lipoatrophy" ]
  ], [
     fhir:index 1600;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002562" ];
     fhir:CodeSystem.concept.display [ fhir:value "Low-set nipples" ]
  ], [
     fhir:index 1601;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012893" ];
     fhir:CodeSystem.concept.display [ fhir:value "Neck muscle hypertrophy" ]
  ], [
     fhir:index 1602;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001027" ];
     fhir:CodeSystem.concept.display [ fhir:value "Soft, doughy skin" ]
  ], [
     fhir:index 1603;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100738" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal eating behavior" ]
  ], [
     fhir:index 1604;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007328" ];
     fhir:CodeSystem.concept.display [ fhir:value "Impaired pain sensation" ]
  ], [
     fhir:index 1605;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002878" ];
     fhir:CodeSystem.concept.display [ fhir:value "Respiratory failure" ]
  ], [
     fhir:index 1606;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001776" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bilateral talipes equinovarus" ]
  ], [
     fhir:index 1607;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001360" ];
     fhir:CodeSystem.concept.display [ fhir:value "Holoprosencephaly" ]
  ], [
     fhir:index 1608;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001973" ];
     fhir:CodeSystem.concept.display [ fhir:value "Autoimmune thrombocytopenia" ]
  ], [
     fhir:index 1609;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100749" ];
     fhir:CodeSystem.concept.display [ fhir:value "Chest pain" ]
  ], [
     fhir:index 1610;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012531" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pain" ]
  ], [
     fhir:index 1611;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007585" ];
     fhir:CodeSystem.concept.display [ fhir:value "Skin fragility with non-scarring blistering" ]
  ], [
     fhir:index 1612;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002108" ];
     fhir:CodeSystem.concept.display [ fhir:value "Spontaneous pneumothorax" ]
  ], [
     fhir:index 1613;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006562" ];
     fhir:CodeSystem.concept.display [ fhir:value "Viral hepatitis" ]
  ], [
     fhir:index 1614;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012647" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal inflammatory response" ]
  ], [
     fhir:index 1615;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012088" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal urinary odor" ]
  ], [
     fhir:index 1616;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011458" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abdominal symptom" ]
  ], [
     fhir:index 1617;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002829" ];
     fhir:CodeSystem.concept.display [ fhir:value "Arthralgia" ]
  ], [
     fhir:index 1618;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010783" ];
     fhir:CodeSystem.concept.display [ fhir:value "Erythema" ]
  ], [
     fhir:index 1619;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010307" ];
     fhir:CodeSystem.concept.display [ fhir:value "Stridor" ]
  ], [
     fhir:index 1620;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001269" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hemiparesis" ]
  ], [
     fhir:index 1621;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006532" ];
     fhir:CodeSystem.concept.display [ fhir:value "Recurrent pneumonia" ]
  ], [
     fhir:index 1622;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002580" ];
     fhir:CodeSystem.concept.display [ fhir:value "Volvulus" ]
  ], [
     fhir:index 1623;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012387" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bronchitis" ]
  ], [
     fhir:index 1624;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001266" ];
     fhir:CodeSystem.concept.display [ fhir:value "Choreoathetosis" ]
  ], [
     fhir:index 1625;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001531" ];
     fhir:CodeSystem.concept.display [ fhir:value "Failure to thrive in infancy" ]
  ], [
     fhir:index 1626;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011470" ];
     fhir:CodeSystem.concept.display [ fhir:value "Nasogastric tube feeding in infancy" ]
  ], [
     fhir:index 1627;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001361" ];
     fhir:CodeSystem.concept.display [ fhir:value "Nystagmus-induced head nodding" ]
  ], [
     fhir:index 1628;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001997" ];
     fhir:CodeSystem.concept.display [ fhir:value "Gout" ]
  ], [
     fhir:index 1629;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000965" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cutis marmorata" ]
  ], [
     fhir:index 1630;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010316" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ebstein anomaly of the tricuspid valve" ]
  ], [
     fhir:index 1631;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010543" ];
     fhir:CodeSystem.concept.display [ fhir:value "Opsoclonus" ]
  ], [
     fhir:index 1632;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007704" ];
     fhir:CodeSystem.concept.display [ fhir:value "Paroxysmal involuntary eye movements" ]
  ], [
     fhir:index 1633;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030364" ];
     fhir:CodeSystem.concept.display [ fhir:value "Secondary Caesarian section" ]
  ], [
     fhir:index 1634;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007738" ];
     fhir:CodeSystem.concept.display [ fhir:value "Uncontrolled eye movements" ]
  ], [
     fhir:index 1635;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030366" ];
     fhir:CodeSystem.concept.display [ fhir:value "Delivery by Odon device" ]
  ], [
     fhir:index 1636;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011411" ];
     fhir:CodeSystem.concept.display [ fhir:value "Forceps delivery" ]
  ], [
     fhir:index 1637;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030369" ];
     fhir:CodeSystem.concept.display [ fhir:value "Induced vaginal delivery" ]
  ], [
     fhir:index 1638;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005268" ];
     fhir:CodeSystem.concept.display [ fhir:value "Spontaneous abortion" ]
  ], [
     fhir:index 1639;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030365" ];
     fhir:CodeSystem.concept.display [ fhir:value "Vaginal birth after Caesarian" ]
  ], [
     fhir:index 1640;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011412" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ventouse delivery" ]
  ], [
     fhir:index 1641;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002572" ];
     fhir:CodeSystem.concept.display [ fhir:value "Episodic vomiting" ]
  ], [
     fhir:index 1642;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030350" ];
     fhir:CodeSystem.concept.display [ fhir:value "Erythematous papule" ]
  ], [
     fhir:index 1643;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001386" ];
     fhir:CodeSystem.concept.display [ fhir:value "Joint swelling" ]
  ], [
     fhir:index 1644;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000147" ];
     fhir:CodeSystem.concept.display [ fhir:value "Polycystic ovaries" ]
  ], [
     fhir:index 1645;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012412" ];
     fhir:CodeSystem.concept.display [ fhir:value "Premature adrenarche" ]
  ], [
     fhir:index 1646;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004411" ];
     fhir:CodeSystem.concept.display [ fhir:value "Deviated nasal septum" ]
  ], [
     fhir:index 1647;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0040183" ];
     fhir:CodeSystem.concept.display [ fhir:value "Encopresis" ]
  ], [
     fhir:index 1648;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100507" ];
     fhir:CodeSystem.concept.display [ fhir:value "Reduced blood folate concentration" ]
  ], [
     fhir:index 1649;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007011" ];
     fhir:CodeSystem.concept.display [ fhir:value "Fourth cranial nerve palsy" ]
  ], [
     fhir:index 1650;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000375" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal cochlea morphology" ]
  ], [
     fhir:index 1651;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009911" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal temporal bone morphology" ]
  ], [
     fhir:index 1652;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000081" ];
     fhir:CodeSystem.concept.display [ fhir:value "Duplicated collecting system" ]
  ], [
     fhir:index 1653;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006894" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoplastic olfactory lobes" ]
  ], [
     fhir:index 1654;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011380" ];
     fhir:CodeSystem.concept.display [ fhir:value "Morphological abnormality of the semicircular canal" ]
  ], [
     fhir:index 1655;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000110" ];
     fhir:CodeSystem.concept.display [ fhir:value "Renal dysplasia" ]
  ], [
     fhir:index 1656;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030025" ];
     fhir:CodeSystem.concept.display [ fhir:value "Auricular pit" ]
  ], [
     fhir:index 1657;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010044" ];
     fhir:CodeSystem.concept.display [ fhir:value "Short 4th metacarpal" ]
  ], [
     fhir:index 1658;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010047" ];
     fhir:CodeSystem.concept.display [ fhir:value "Short 5th metacarpal" ]
  ], [
     fhir:index 1659;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000201" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pierre-Robin sequence" ]
  ], [
     fhir:index 1660;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100837" ];
     fhir:CodeSystem.concept.display [ fhir:value "Atrophodermia vermiculata" ]
  ], [
     fhir:index 1661;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002673" ];
     fhir:CodeSystem.concept.display [ fhir:value "Coxa valga" ]
  ], [
     fhir:index 1662;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001476" ];
     fhir:CodeSystem.concept.display [ fhir:value "Delayed closure of the anterior fontanelle" ]
  ], [
     fhir:index 1663;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011069" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased number of teeth" ]
  ], [
     fhir:index 1664;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009879" ];
     fhir:CodeSystem.concept.display [ fhir:value "Simplified gyral pattern" ]
  ], [
     fhir:index 1665;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006315" ];
     fhir:CodeSystem.concept.display [ fhir:value "Single median maxillary incisor" ]
  ], [
     fhir:index 1666;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001194" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormalities of placenta or umbilical cord" ]
  ], [
     fhir:index 1667;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100767" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal placenta morphology" ]
  ], [
     fhir:index 1668;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006543" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cardiorespiratory arrest" ]
  ], [
     fhir:index 1669;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003074" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyperglycemia" ]
  ], [
     fhir:index 1670;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000842" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyperinsulinemia" ]
  ], [
     fhir:index 1671;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011951" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aspiration pneumonia" ]
  ], [
     fhir:index 1672;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006528" ];
     fhir:CodeSystem.concept.display [ fhir:value "Chronic lung disease" ]
  ], [
     fhir:index 1673;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002383" ];
     fhir:CodeSystem.concept.display [ fhir:value "Encephalitis" ]
  ], [
     fhir:index 1674;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000388" ];
     fhir:CodeSystem.concept.display [ fhir:value "Otitis media" ]
  ], [
     fhir:index 1675;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002530" ];
     fhir:CodeSystem.concept.display [ fhir:value "Axial dystonia" ]
  ], [
     fhir:index 1676;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002780" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bronchomalacia" ]
  ], [
     fhir:index 1677;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008755" ];
     fhir:CodeSystem.concept.display [ fhir:value "Laryngotracheomalacia" ]
  ], [
     fhir:index 1678;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000308" ];
     fhir:CodeSystem.concept.display [ fhir:value "Microretrognathia" ]
  ], [
     fhir:index 1679;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002786" ];
     fhir:CodeSystem.concept.display [ fhir:value "Tracheobronchomalacia" ]
  ], [
     fhir:index 1680;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012389" ];
     fhir:CodeSystem.concept.display [ fhir:value "Appendicular hypotonia" ]
  ], [
     fhir:index 1681;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011323" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cleft of chin" ]
  ], [
     fhir:index 1682;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000417" ];
     fhir:CodeSystem.concept.display [ fhir:value "Slender nose" ]
  ], [
     fhir:index 1683;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001863" ];
     fhir:CodeSystem.concept.display [ fhir:value "Toe clinodactyly" ]
  ], [
     fhir:index 1684;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008386" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aplasia/Hypoplasia of the nails" ]
  ], [
     fhir:index 1685;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006989" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dysplastic corpus callosum" ]
  ], [
     fhir:index 1686;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100954" ];
     fhir:CodeSystem.concept.display [ fhir:value "Open operculum" ]
  ], [
     fhir:index 1687;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004482" ];
     fhir:CodeSystem.concept.display [ fhir:value "Relative macrocephaly" ]
  ], [
     fhir:index 1688;
     fhir:CodeSystem.concept.code [ fhir:value "HP:3000033" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal nasopharyngeal adenoid morphology" ]
  ], [
     fhir:index 1689;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009062" ];
     fhir:CodeSystem.concept.display [ fhir:value "Infantile axial hypotonia" ]
  ], [
     fhir:index 1690;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002189" ];
     fhir:CodeSystem.concept.display [ fhir:value "obsolete Excessive daytime sleepiness" ]
  ], [
     fhir:index 1691;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002141" ];
     fhir:CodeSystem.concept.display [ fhir:value "Gait imbalance" ]
  ], [
     fhir:index 1692;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012734" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ketotic hypoglycemia" ]
  ], [
     fhir:index 1693;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005968" ];
     fhir:CodeSystem.concept.display [ fhir:value "Temperature instability" ]
  ], [
     fhir:index 1694;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012538" ];
     fhir:CodeSystem.concept.display [ fhir:value "Gluten intolerance" ]
  ], [
     fhir:index 1695;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000979" ];
     fhir:CodeSystem.concept.display [ fhir:value "Purpura" ]
  ], [
     fhir:index 1696;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001988" ];
     fhir:CodeSystem.concept.display [ fhir:value "Recurrent hypoglycemia" ]
  ], [
     fhir:index 1697;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001488" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bilateral ptosis" ]
  ], [
     fhir:index 1698;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011229" ];
     fhir:CodeSystem.concept.display [ fhir:value "Broad eyebrow" ]
  ], [
     fhir:index 1699;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004440" ];
     fhir:CodeSystem.concept.display [ fhir:value "Coronal craniosynostosis" ]
  ], [
     fhir:index 1700;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004453" ];
     fhir:CodeSystem.concept.display [ fhir:value "Overfolding of the superior helices" ]
  ], [
     fhir:index 1701;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012547" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal involuntary eye movements" ]
  ], [
     fhir:index 1702;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100814" ];
     fhir:CodeSystem.concept.display [ fhir:value "Blue nevus" ]
  ], [
     fhir:index 1703;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010751" ];
     fhir:CodeSystem.concept.display [ fhir:value "Dimple chin" ]
  ], [
     fhir:index 1704;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007087" ];
     fhir:CodeSystem.concept.display [ fhir:value "obsolete Involuntary jerking movements" ]
  ], [
     fhir:index 1705;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012498" ];
     fhir:CodeSystem.concept.display [ fhir:value "Nuchal cord" ]
  ], [
     fhir:index 1706;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002472" ];
     fhir:CodeSystem.concept.display [ fhir:value "Small cerebral cortex" ]
  ], [
     fhir:index 1707;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100307" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cerebellar hemisphere hypoplasia" ]
  ], [
     fhir:index 1708;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002151" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased serum lactate" ]
  ], [
     fhir:index 1709;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001698" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pericardial effusion" ]
  ], [
     fhir:index 1710;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006903" ];
     fhir:CodeSystem.concept.display [ fhir:value "Congenital peripheral neuropathy" ]
  ], [
     fhir:index 1711;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006895" ];
     fhir:CodeSystem.concept.display [ fhir:value "Lower limb hypertonia" ]
  ], [
     fhir:index 1712;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002744" ];
     fhir:CodeSystem.concept.display [ fhir:value "Bilateral cleft lip and palate" ]
  ], [
     fhir:index 1713;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010664" ];
     fhir:CodeSystem.concept.display [ fhir:value "Fusion of the left and right thalami" ]
  ], [
     fhir:index 1714;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000327" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoplasia of the maxilla" ]
  ], [
     fhir:index 1715;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000474" ];
     fhir:CodeSystem.concept.display [ fhir:value "Thickened nuchal skin fold" ]
  ], [
     fhir:index 1716;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000105" ];
     fhir:CodeSystem.concept.display [ fhir:value "Enlarged kidney" ]
  ], [
     fhir:index 1717;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000113" ];
     fhir:CodeSystem.concept.display [ fhir:value "Polycystic kidney dysplasia" ]
  ], [
     fhir:index 1718;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000104" ];
     fhir:CodeSystem.concept.display [ fhir:value "Renal agenesis" ]
  ], [
     fhir:index 1719;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001362" ];
     fhir:CodeSystem.concept.display [ fhir:value "Calvarial skull defect" ]
  ], [
     fhir:index 1720;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008245" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pituitary hypothyroidism" ]
  ], [
     fhir:index 1721;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001552" ];
     fhir:CodeSystem.concept.display [ fhir:value "Barrel-shaped chest" ]
  ], [
     fhir:index 1722;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006297" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoplasia of dental enamel" ]
  ], [
     fhir:index 1723;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100023" ];
     fhir:CodeSystem.concept.display [ fhir:value "Recurrent hand flapping" ]
  ], [
     fhir:index 1724;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005518" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased mean corpuscular volume" ]
  ], [
     fhir:index 1725;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012418" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoxemia" ]
  ], [
     fhir:index 1726;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100259" ];
     fhir:CodeSystem.concept.display [ fhir:value "Postaxial polydactyly" ]
  ], [
     fhir:index 1727;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010814" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal position of hair whorl" ]
  ], [
     fhir:index 1728;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003764" ];
     fhir:CodeSystem.concept.display [ fhir:value "Nevus" ]
  ], [
     fhir:index 1729;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000445" ];
     fhir:CodeSystem.concept.display [ fhir:value "Wide nose" ]
  ], [
     fhir:index 1730;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010677" ];
     fhir:CodeSystem.concept.display [ fhir:value "Enuresis nocturna" ]
  ], [
     fhir:index 1731;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001510" ];
     fhir:CodeSystem.concept.display [ fhir:value "Growth delay" ]
  ], [
     fhir:index 1732;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012428" ];
     fhir:CodeSystem.concept.display [ fhir:value "Prominent calcaneus" ]
  ], [
     fhir:index 1733;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012471" ];
     fhir:CodeSystem.concept.display [ fhir:value "Thick vermilion border" ]
  ], [
     fhir:index 1734;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007110" ];
     fhir:CodeSystem.concept.display [ fhir:value "Central hypoventilation" ]
  ], [
     fhir:index 1735;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010614" ];
     fhir:CodeSystem.concept.display [ fhir:value "Fibroma" ]
  ], [
     fhir:index 1736;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001034" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypermelanotic macule" ]
  ], [
     fhir:index 1737;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011365" ];
     fhir:CodeSystem.concept.display [ fhir:value "Patchy hypopigmentation of hair" ]
  ], [
     fhir:index 1738;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001920" ];
     fhir:CodeSystem.concept.display [ fhir:value "Renal artery stenosis" ]
  ], [
     fhir:index 1739;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002828" ];
     fhir:CodeSystem.concept.display [ fhir:value "Multiple joint contractures" ]
  ], [
     fhir:index 1740;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002144" ];
     fhir:CodeSystem.concept.display [ fhir:value "Tethered cord" ]
  ], [
     fhir:index 1741;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010964" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal circulating long-chain fatty-acid concentration" ]
  ], [
     fhir:index 1742;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010536" ];
     fhir:CodeSystem.concept.display [ fhir:value "Central sleep apnea" ]
  ], [
     fhir:index 1743;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011262" ];
     fhir:CodeSystem.concept.display [ fhir:value "Crimped helix" ]
  ], [
     fhir:index 1744;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0040079" ];
     fhir:CodeSystem.concept.display [ fhir:value "Irregular dentition" ]
  ], [
     fhir:index 1745;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011481" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal lacrimal duct morphology" ]
  ], [
     fhir:index 1746;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000220" ];
     fhir:CodeSystem.concept.display [ fhir:value "Velopharyngeal insufficiency" ]
  ], [
     fhir:index 1747;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002153" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyperkalemia" ]
  ], [
     fhir:index 1748;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002148" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypophosphatemia" ]
  ], [
     fhir:index 1749;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012621" ];
     fhir:CodeSystem.concept.display [ fhir:value "Persistent cloaca" ]
  ], [
     fhir:index 1750;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000867" ];
     fhir:CodeSystem.concept.display [ fhir:value "Secondary hyperparathyroidism" ]
  ], [
     fhir:index 1751;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003762" ];
     fhir:CodeSystem.concept.display [ fhir:value "Uterus didelphys" ]
  ], [
     fhir:index 1752;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100512" ];
     fhir:CodeSystem.concept.display [ fhir:value "Low levels of vitamin D" ]
  ], [
     fhir:index 1753;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012156" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hemophagocytosis" ]
  ], [
     fhir:index 1754;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008209" ];
     fhir:CodeSystem.concept.display [ fhir:value "Premature ovarian insufficiency" ]
  ], [
     fhir:index 1755;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004349" ];
     fhir:CodeSystem.concept.display [ fhir:value "Reduced bone mineral density" ]
  ], [
     fhir:index 1756;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001924" ];
     fhir:CodeSystem.concept.display [ fhir:value "Sideroblastic anemia" ]
  ], [
     fhir:index 1757;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011703" ];
     fhir:CodeSystem.concept.display [ fhir:value "Sinus tachycardia" ]
  ], [
     fhir:index 1758;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010609" ];
     fhir:CodeSystem.concept.display [ fhir:value "Skin tags" ]
  ], [
     fhir:index 1759;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002725" ];
     fhir:CodeSystem.concept.display [ fhir:value "Systemic lupus erythematosus" ]
  ], [
     fhir:index 1760;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003193" ];
     fhir:CodeSystem.concept.display [ fhir:value "Allergic rhinitis" ]
  ], [
     fhir:index 1761;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006896" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypnopompic hallucinations" ]
  ], [
     fhir:index 1762;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002524" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cataplexy" ]
  ], [
     fhir:index 1763;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005227" ];
     fhir:CodeSystem.concept.display [ fhir:value "Adenomatous colonic polyposis" ]
  ], [
     fhir:index 1764;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012173" ];
     fhir:CodeSystem.concept.display [ fhir:value "Orthostatic tachycardia" ]
  ], [
     fhir:index 1765;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001271" ];
     fhir:CodeSystem.concept.display [ fhir:value "Polyneuropathy" ]
  ], [
     fhir:index 1766;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009120" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aplasia/Hypoplasia involving the sinuses" ]
  ], [
     fhir:index 1767;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000625" ];
     fhir:CodeSystem.concept.display [ fhir:value "Eyelid coloboma" ]
  ], [
     fhir:index 1768;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009754" ];
     fhir:CodeSystem.concept.display [ fhir:value "Fibrous syngnathia" ]
  ], [
     fhir:index 1769;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012478" ];
     fhir:CodeSystem.concept.display [ fhir:value "Temporomandibular joint ankylosis" ]
  ], [
     fhir:index 1770;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001233" ];
     fhir:CodeSystem.concept.display [ fhir:value "2-3 finger syndactyly" ]
  ], [
     fhir:index 1771;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000811" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal external genitalia" ]
  ], [
     fhir:index 1772;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005120" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal cardiac atrium morphology" ]
  ], [
     fhir:index 1773;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008388" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal toenail morphology" ]
  ], [
     fhir:index 1774;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011467" ];
     fhir:CodeSystem.concept.display [ fhir:value "Absent gallbladder" ]
  ], [
     fhir:index 1775;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010760" ];
     fhir:CodeSystem.concept.display [ fhir:value "Absent toe" ]
  ], [
     fhir:index 1776;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001545" ];
     fhir:CodeSystem.concept.display [ fhir:value "Anteriorly placed anus" ]
  ], [
     fhir:index 1777;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001640" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cardiomegaly" ]
  ], [
     fhir:index 1778;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002990" ];
     fhir:CodeSystem.concept.display [ fhir:value "Fibular aplasia" ]
  ], [
     fhir:index 1779;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004443" ];
     fhir:CodeSystem.concept.display [ fhir:value "Lambdoidal craniosynostosis" ]
  ], [
     fhir:index 1780;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008569" ];
     fhir:CodeSystem.concept.display [ fhir:value "Microtia, second degree" ]
  ], [
     fhir:index 1781;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006277" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pancreatic hyperplasia" ]
  ], [
     fhir:index 1782;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010445" ];
     fhir:CodeSystem.concept.display [ fhir:value "Primum atrial septal defect" ]
  ], [
     fhir:index 1783;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011640" ];
     fhir:CodeSystem.concept.display [ fhir:value "Single coronary artery origin" ]
  ], [
     fhir:index 1784;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011608" ];
     fhir:CodeSystem.concept.display [ fhir:value "Type II truncus arteriosus" ]
  ], [
     fhir:index 1785;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011327" ];
     fhir:CodeSystem.concept.display [ fhir:value "Posterior plagiocephaly" ]
  ], [
     fhir:index 1786;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007655" ];
     fhir:CodeSystem.concept.display [ fhir:value "Eversion of lateral third of lower eyelids" ]
  ], [
     fhir:index 1787;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010747" ];
     fhir:CodeSystem.concept.display [ fhir:value "Medial flaring of the eyebrow" ]
  ], [
     fhir:index 1788;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005957" ];
     fhir:CodeSystem.concept.display [ fhir:value "Breathing dysregulation" ]
  ], [
     fhir:index 1789;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000992" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cutaneous photosensitivity" ]
  ], [
     fhir:index 1790;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011995" ];
     fhir:CodeSystem.concept.display [ fhir:value "Atrial septal dilatation" ]
  ], [
     fhir:index 1791;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000377" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the pinna" ]
  ], [
     fhir:index 1792;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011266" ];
     fhir:CodeSystem.concept.display [ fhir:value "Microtia, first degree" ]
  ], [
     fhir:index 1793;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012650" ];
     fhir:CodeSystem.concept.display [ fhir:value "Perisylvian polymicrogyria" ]
  ], [
     fhir:index 1794;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004970" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ascending tubular aorta aneurysm" ]
  ], [
     fhir:index 1795;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008348" ];
     fhir:CodeSystem.concept.display [ fhir:value "Decreased circulating IgG2 level" ]
  ], [
     fhir:index 1796;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012115" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hepatitis" ]
  ], [
     fhir:index 1797;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006979" ];
     fhir:CodeSystem.concept.display [ fhir:value "Sleep-wake cycle disturbance" ]
  ], [
     fhir:index 1798;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008587" ];
     fhir:CodeSystem.concept.display [ fhir:value "Mild neurosensory hearing impairment" ]
  ], [
     fhir:index 1799;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006097" ];
     fhir:CodeSystem.concept.display [ fhir:value "3-4 finger syndactyly" ]
  ], [
     fhir:index 1800;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005263" ];
     fhir:CodeSystem.concept.display [ fhir:value "Gastritis" ]
  ], [
     fhir:index 1801;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0200043" ];
     fhir:CodeSystem.concept.display [ fhir:value "Verrucae" ]
  ], [
     fhir:index 1802;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009600" ];
     fhir:CodeSystem.concept.display [ fhir:value "Flexion contracture of thumb" ]
  ], [
     fhir:index 1803;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010818" ];
     fhir:CodeSystem.concept.display [ fhir:value "Generalized tonic seizure" ]
  ], [
     fhir:index 1804;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002599" ];
     fhir:CodeSystem.concept.display [ fhir:value "Head titubation" ]
  ], [
     fhir:index 1805;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002090" ];
     fhir:CodeSystem.concept.display [ fhir:value "Pneumonia" ]
  ], [
     fhir:index 1806;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030423" ];
     fhir:CodeSystem.concept.display [ fhir:value "Splenic cyst" ]
  ], [
     fhir:index 1807;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0030187" ];
     fhir:CodeSystem.concept.display [ fhir:value "Titubation" ]
  ], [
     fhir:index 1808;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002375" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypokinesia" ]
  ], [
     fhir:index 1809;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007166" ];
     fhir:CodeSystem.concept.display [ fhir:value "Paroxysmal dyskinesia" ]
  ], [
     fhir:index 1810;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003077" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hyperlipidemia" ]
  ], [
     fhir:index 1811;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000017" ];
     fhir:CodeSystem.concept.display [ fhir:value "Nocturia" ]
  ], [
     fhir:index 1812;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100555" ];
     fhir:CodeSystem.concept.display [ fhir:value "Asymmetric growth" ]
  ], [
     fhir:index 1813;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011847" ];
     fhir:CodeSystem.concept.display [ fhir:value "Giant cell tumor of bone" ]
  ], [
     fhir:index 1814;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000112" ];
     fhir:CodeSystem.concept.display [ fhir:value "Nephropathy" ]
  ], [
     fhir:index 1815;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000246" ];
     fhir:CodeSystem.concept.display [ fhir:value "Sinusitis" ]
  ], [
     fhir:index 1816;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001012" ];
     fhir:CodeSystem.concept.display [ fhir:value "Multiple lipomas" ]
  ], [
     fhir:index 1817;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000851" ];
     fhir:CodeSystem.concept.display [ fhir:value "Congenital hypothyroidism" ]
  ], [
     fhir:index 1818;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002345" ];
     fhir:CodeSystem.concept.display [ fhir:value "Action tremor" ]
  ], [
     fhir:index 1819;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002677" ];
     fhir:CodeSystem.concept.display [ fhir:value "Small foramen magnum" ]
  ], [
     fhir:index 1820;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011947" ];
     fhir:CodeSystem.concept.display [ fhir:value "Respiratory tract infection" ]
  ], [
     fhir:index 1821;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012151" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hemothorax" ]
  ], [
     fhir:index 1822;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005988" ];
     fhir:CodeSystem.concept.display [ fhir:value "Congenital muscular torticollis" ]
  ], [
     fhir:index 1823;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002329" ];
     fhir:CodeSystem.concept.display [ fhir:value "Drowsiness" ]
  ], [
     fhir:index 1824;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012395" ];
     fhir:CodeSystem.concept.display [ fhir:value "Seasonal allergy" ]
  ], [
     fhir:index 1825;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011679" ];
     fhir:CodeSystem.concept.display [ fhir:value "Tetralogy of Fallot with pulmonary stenosis" ]
  ], [
     fhir:index 1826;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001864" ];
     fhir:CodeSystem.concept.display [ fhir:value "Clinodactyly of the 5th toe" ]
  ], [
     fhir:index 1827;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006934" ];
     fhir:CodeSystem.concept.display [ fhir:value "Congenital nystagmus" ]
  ], [
     fhir:index 1828;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100355" ];
     fhir:CodeSystem.concept.display [ fhir:value "Contractures of the distal interphalangeal joint of the 5th toe" ]
  ], [
     fhir:index 1829;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007894" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypopigmentation of the fundus" ]
  ], [
     fhir:index 1830;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012377" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hemianopia" ]
  ], [
     fhir:index 1831;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002354" ];
     fhir:CodeSystem.concept.display [ fhir:value "Memory impairment" ]
  ], [
     fhir:index 1832;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000872" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hashimoto thyroiditis" ]
  ], [
     fhir:index 1833;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002519" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypnagogic hallucinations" ]
  ], [
     fhir:index 1834;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010647" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal elasticity of skin" ]
  ], [
     fhir:index 1835;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002592" ];
     fhir:CodeSystem.concept.display [ fhir:value "Gastric ulcer" ]
  ], [
     fhir:index 1836;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004938" ];
     fhir:CodeSystem.concept.display [ fhir:value "Tortuous cerebral arteries" ]
  ], [
     fhir:index 1837;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004948" ];
     fhir:CodeSystem.concept.display [ fhir:value "Vascular tortuosity" ]
  ], [
     fhir:index 1838;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002516" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased intracranial pressure" ]
  ], [
     fhir:index 1839;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006460" ];
     fhir:CodeSystem.concept.display [ fhir:value "Increased laxity of ankles" ]
  ], [
     fhir:index 1840;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002317" ];
     fhir:CodeSystem.concept.display [ fhir:value "Unsteady gait" ]
  ], [
     fhir:index 1841;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000182" ];
     fhir:CodeSystem.concept.display [ fhir:value "Movement abnormality of the tongue" ]
  ], [
     fhir:index 1842;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009887" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of hair pigmentation" ]
  ], [
     fhir:index 1843;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005824" ];
     fhir:CodeSystem.concept.display [ fhir:value "Clinodactyly of the 2nd toe" ]
  ], [
     fhir:index 1844;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002212" ];
     fhir:CodeSystem.concept.display [ fhir:value "Curly hair" ]
  ], [
     fhir:index 1845;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0009803" ];
     fhir:CodeSystem.concept.display [ fhir:value "Short phalanx of finger" ]
  ], [
     fhir:index 1846;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000572" ];
     fhir:CodeSystem.concept.display [ fhir:value "Visual loss" ]
  ], [
     fhir:index 1847;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0005216" ];
     fhir:CodeSystem.concept.display [ fhir:value "Impaired mastication" ]
  ], [
     fhir:index 1848;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0000619" ];
     fhir:CodeSystem.concept.display [ fhir:value "Impaired convergence" ]
  ], [
     fhir:index 1849;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002403" ];
     fhir:CodeSystem.concept.display [ fhir:value "Positive Romberg sign" ]
  ], [
     fhir:index 1850;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008744" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal aryepiglottic fold morphology" ]
  ], [
     fhir:index 1851;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002374" ];
     fhir:CodeSystem.concept.display [ fhir:value "Diminished movement" ]
  ], [
     fhir:index 1852;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008277" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal blood zinc concentration" ]
  ], [
     fhir:index 1853;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012781" ];
     fhir:CodeSystem.concept.display [ fhir:value "Mid-frequency hearing loss" ]
  ], [
     fhir:index 1854;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0100758" ];
     fhir:CodeSystem.concept.display [ fhir:value "Gangrene" ]
  ], [
     fhir:index 1855;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003256" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of the coagulation cascade" ]
  ], [
     fhir:index 1856;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004387" ];
     fhir:CodeSystem.concept.display [ fhir:value "Enterocolitis" ]
  ], [
     fhir:index 1857;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011029" ];
     fhir:CodeSystem.concept.display [ fhir:value "Internal hemorrhage" ]
  ], [
     fhir:index 1858;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011649" ];
     fhir:CodeSystem.concept.display [ fhir:value "Patent ductus arteriosus after premature birth" ]
  ], [
     fhir:index 1859;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0012050" ];
     fhir:CodeSystem.concept.display [ fhir:value "Anasarca" ]
  ], [
     fhir:index 1860;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001683" ];
     fhir:CodeSystem.concept.display [ fhir:value "Ectopia cordis" ]
  ], [
     fhir:index 1861;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011682" ];
     fhir:CodeSystem.concept.display [ fhir:value "Perimembranous ventricular septal defect" ]
  ], [
     fhir:index 1862;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0010624" ];
     fhir:CodeSystem.concept.display [ fhir:value "Aplastic/hypoplastic toenail" ]
  ], [
     fhir:index 1863;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002705" ];
     fhir:CodeSystem.concept.display [ fhir:value "High, narrow palate" ]
  ], [
     fhir:index 1864;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011340" ];
     fhir:CodeSystem.concept.display [ fhir:value "Incomplete cleft of the upper lip" ]
  ], [
     fhir:index 1865;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011613" ];
     fhir:CodeSystem.concept.display [ fhir:value "Interrupted aortic arch type B" ]
  ], [
     fhir:index 1866;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006167" ];
     fhir:CodeSystem.concept.display [ fhir:value "Prominent proximal interphalangeal joints" ]
  ], [
     fhir:index 1867;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002918" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypermagnesemia" ]
  ], [
     fhir:index 1868;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011937" ];
     fhir:CodeSystem.concept.display [ fhir:value "Hypoplastic fifth toenail" ]
  ], [
     fhir:index 1869;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0001067" ];
     fhir:CodeSystem.concept.display [ fhir:value "Neurofibromas" ]
  ], [
     fhir:index 1870;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011403" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormal umbilical cord blood vessels" ]
  ], [
     fhir:index 1871;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0003316" ];
     fhir:CodeSystem.concept.display [ fhir:value "Butterfly vertebrae" ]
  ], [
     fhir:index 1872;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002247" ];
     fhir:CodeSystem.concept.display [ fhir:value "Duodenal atresia" ]
  ], [
     fhir:index 1873;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008439" ];
     fhir:CodeSystem.concept.display [ fhir:value "Lumbar hemivertebrae" ]
  ], [
     fhir:index 1874;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0011599" ];
     fhir:CodeSystem.concept.display [ fhir:value "Mesocardia" ]
  ], [
     fhir:index 1875;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0008467" ];
     fhir:CodeSystem.concept.display [ fhir:value "Thoracic hemivertebrae" ]
  ], [
     fhir:index 1876;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0004626" ];
     fhir:CodeSystem.concept.display [ fhir:value "Lumbar scoliosis" ]
  ], [
     fhir:index 1877;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0006808" ];
     fhir:CodeSystem.concept.display [ fhir:value "Cerebral hypomyelination" ]
  ], [
     fhir:index 1878;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0002926" ];
     fhir:CodeSystem.concept.display [ fhir:value "Abnormality of thyroid physiology" ]
  ], [
     fhir:index 1879;
     fhir:CodeSystem.concept.code [ fhir:value "HP:0007970" ];
     fhir:CodeSystem.concept.display [ fhir:value "Congenital ptosis" ]
  ]. # 

# - ontology header ------------------------------------------------------------

 a owl:Ontology;
  owl:imports fhir:fhir.ttl.