FHIR © HL7.org  |  FHIRsmith 4.0.1  |  Server Home  |  XIG Home  |  XIG Stats  | 

FHIR IG analytics

Packageus.nlm.vsac
Resource TypeValueSet
IdValueSet-2.16.840.1.113762.1.4.1247.137.json
FHIR VersionR4
Sourcehttps://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1247.137/expansion
URLhttp://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1247.137
Version20240626
Statusactive
Date2024-06-26T01:12:04-04:00
NameCognitiveDisorderDiagnosis
TitleCognitive disorder Diagnosis
Realmus
Authorityhl7
Purpose(Clinical Focus: This set of values contains diagnosis terms representing cognitive disorder.),(Data Element Scope: The intent of this set of values is to identify patients who have a diagnosis of cognitive disorder.),(Inclusion Criteria: Includes cognitive disorder diagnosis concepts from SNOMED CT and ICD-10-CM.),(Exclusion Criteria: None)

Resources that use this resource

No resources found


Resources that this resource uses

CodeSystem
icd-10-cmInternational Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM)
sctSNOMED codes used in this IG
ValueSet
2.16.840.1.113762.1.4.1222.1525Cognitive disorder Diagnosis ICD10
2.16.840.1.113762.1.4.1222.1526Cognitive disorder SCT

Narrative

No narrative content found in resource


Source1

{
  "resourceType": "ValueSet",
  "id": "2.16.840.1.113762.1.4.1247.137",
  "meta": {
    "versionId": "13",
    "lastUpdated": "2024-09-12T09:47:35.000-04:00",
    "profile": [
      "http://hl7.org/fhir/StructureDefinition/shareablevalueset",
      "http://hl7.org/fhir/us/cqfmeasures/StructureDefinition/computable-valueset-cqfm",
      "http://hl7.org/fhir/us/cqfmeasures/StructureDefinition/publishable-valueset-cqfm"
    ]
  },
  "extension": [
    {
      "url": "http://hl7.org/fhir/StructureDefinition/valueset-author",
      "valueContactDetail": {
        "name": "MCC eCare Plan Author"
      }
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/valueset-keyWord",
      "valueString": "MCC_IG"
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate",
      "valueDate": "2024-06-26"
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate",
      "valueDate": "2024-06-26"
    }
  ],
  "url": "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1247.137",
  "identifier": [
    {
      "system": "urn:ietf:rfc:3986",
      "value": "urn:oid:2.16.840.1.113762.1.4.1247.137"
    }
  ],
  "version": "20240626",
  "name": "CognitiveDisorderDiagnosis",
  "title": "Cognitive disorder Diagnosis",
  "status": "active",
  "date": "2024-06-26T01:12:04-04:00",
  "publisher": "HL7 Patient Care WG Steward",
  "jurisdiction": [
    {
      "coding": [
        {
          "system": "urn:iso:std:iso:3166",
          "code": "US"
        }
      ]
    }
  ],
  "purpose": "(Clinical Focus: This set of values contains diagnosis terms representing cognitive disorder.),(Data Element Scope: The intent of this set of values is to identify patients who have a diagnosis of cognitive disorder.),(Inclusion Criteria: Includes cognitive disorder diagnosis concepts from SNOMED CT and ICD-10-CM.),(Exclusion Criteria: None)",
  "compose": {
    "include": [
      {
        "valueSet": [
          "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1222.1525"
        ]
      },
      {
        "valueSet": [
          "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1222.1526"
        ]
      }
    ]
  },
  "expansion": {
    "identifier": "urn:uuid:869d0a5f-03f2-41fd-ba5f-4f5b1a2acbe7",
    "timestamp": "2025-05-23T20:45:30-04:00",
    "total": 1054,
    "contains": [
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "10007009",
        "display": "Coffin-Siris syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1003385006",
        "display": "Neurodevelopmental disorder due to maternal use of alcohol (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1010630006",
        "display": "X-linked complicated corpus callosum dysgenesis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "101421000119107",
        "display": "Dementia due to Parkinson's disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "10349009",
        "display": "Multi-infarct dementia with delirium (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "10532003",
        "display": "Primary degenerative dementia of the Alzheimer type, presenile onset, with depression (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "105421000119105",
        "display": "Early onset Alzheimer's disease with behavioral disturbance (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "106021000119105",
        "display": "Multi-infarct dementia due to atherosclerosis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "109478007",
        "display": "Kohlschutter's syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "110359009",
        "display": "Intellectual disability (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "111477005",
        "display": "Reactive attachment disorder of infancy OR early childhood, disinhibited type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "111480006",
        "display": "Psychoactive substance-induced organic dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1148924004",
        "display": "Dementia due to deficiency of folic acid (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1156584007",
        "display": "X-linked intellectual disability hypotonic face syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1156789004",
        "display": "Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1156798001",
        "display": "Autosomal dominant Alzheimer disease due to mutation of presenilin 2 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1156800008",
        "display": "Autosomal dominant Alzheimer disease due to mutation of presenilin 1 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1162462009",
        "display": "Angelman syndrome due to maternal monosomy 15q11q13 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1163406003",
        "display": "Foreign accent syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1167371007",
        "display": "Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1167375003",
        "display": "Microcephaly, corpus callosum and cerebellar vermis hypoplasia, facial dysmorphism, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1169355000",
        "display": "Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1169359006",
        "display": "Tall stature, intellectual disability, renal anomalies syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1172594000",
        "display": "Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1172624000",
        "display": "Arginine-glutamic acid dipeptide repeats-related neurodevelopmental syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1172626003",
        "display": "Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1172627007",
        "display": "Early-onset epilepsy, intellectual disability, brain anomalies syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1172629005",
        "display": "Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1172630000",
        "display": "Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1172685001",
        "display": "Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1172691004",
        "display": "Chloride voltage-gated channel 4-related X-linked intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1172697000",
        "display": "X-linked female restricted facial dysmorphism, short stature, choanal atresia, intellectual disability (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1172698005",
        "display": "Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1172844009",
        "display": "Combined oxidative phosphorylation defect type 27 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1172889005",
        "display": "Palatal anomalies, widely spaced teeth, facial dysmorphism, developmental delay syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1172899000",
        "display": "Peripheral myelin protein 22-retinoic acid induced 1 contiguous gene duplication syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1173036000",
        "display": "Combined oxidative phosphorylation defect type 23 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1173998003",
        "display": "Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1177167002",
        "display": "Intellectual disability, seizures, abnormal gait, facial dysmorphism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1177169004",
        "display": "Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1177175008",
        "display": "Skeletal dysplasia, T-cell immunodeficiency, developmental delay syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1179282009",
        "display": "Severe neurodevelopmental disorder with feeding difficulties, stereotypic hand movement, bilateral cataract (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1179283004",
        "display": "Metopic ridging, ptosis, facial dysmorphism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1179301003",
        "display": "Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1179408008",
        "display": "Chromodomain helicase dna-binding protein 3- related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1186711002",
        "display": "G protein subunit beta 5-related intellectual disability, cardiac arrhythmia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1186713004",
        "display": "Growth delay, intellectual disability, hepatopathy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1186721005",
        "display": "Infantile inflammatory bowel disease with neurological involvement (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1186724002",
        "display": "HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1186729007",
        "display": "Intellectual disability, cardiac anomalies, short stature, joint laxity syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1186730002",
        "display": "Gabriele-de Vries syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1186734006",
        "display": "Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1186821000",
        "display": "Developmental academic disorder due to deficiency of micronutrients (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1186823002",
        "display": "Developmental academic disorder due to nutritional stunting (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1186826005",
        "display": "Developmental academic disorder due to iron deficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1186832000",
        "display": "Developmental academic disorder due to iodine deficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1186839009",
        "display": "Cognitive impairment due to lead toxicity (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1186877003",
        "display": "Dementia due to vitamin E deficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1186879000",
        "display": "Dementia due to thiamine deficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1186880002",
        "display": "Dementia due to cobalamin deficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1186881003",
        "display": "Dementia due to niacin deficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1186883000",
        "display": "Dementia due to nutritional deficiency disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1186887004",
        "display": "Dementia caused by manganese and/or manganese compound (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1187004001",
        "display": "Chronic traumatic encephalopathy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1187038009",
        "display": "Non-specific syndromic intellectual disability (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1187041000",
        "display": "Stromal antigen 1-related intellectual disability, facial dysmorphism, gastroesophageal reflux syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1187042007",
        "display": "Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1187114007",
        "display": "Micrognathia, recurrent infections, behavioral abnormalities, mild intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1187122000",
        "display": "Witteveen Kolk syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1187126002",
        "display": "Integral membrane protein 2B related amyloidosis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1187195007",
        "display": "Microcephalic cortical malformations, short stature due to rotatin deficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1187210007",
        "display": "Intellectual disability, epilepsy, extrapyramidal syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1187247007",
        "display": "WW domain containing adaptor with coiled-coil-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1187249005",
        "display": "VPS11 core subunit of CORVET and HOPS complexes-related autosomal recessive hypomyelinating leukodystrophy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1187250005",
        "display": "Seizures, scoliosis, macrocephaly syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1187277001",
        "display": "Short stature, brachydactyly, obesity, global developmental delay syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1187278006",
        "display": "Spastic paraplegia, severe developmental delay, epilepsy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1187303004",
        "display": "Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1187304005",
        "display": "Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1187642008",
        "display": "Macrocephaly, intellectual disability, left ventricular non compaction syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1187644009",
        "display": "Basel Vanagaite Smirin Yosef syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1197148005",
        "display": "Sanjad Sakati syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1197587003",
        "display": "Lethal neonatal spasticity, epileptic encephalopathy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1197588008",
        "display": "X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1197591008",
        "display": "Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1197593006",
        "display": "Intellectual disability, expressive aphasia, facial dysmorphism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1208341008",
        "display": "Severe oculo-renal-cerebellar syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1208344000",
        "display": "Fryns Smeets Thiry syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1208481000",
        "display": "Progressive cerebello-cerebral atrophy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1208486005",
        "display": "Multiple mitochondrial dysfunctions syndrome type 2 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1208488006",
        "display": "Special AT-rich sequence-binding protein 2-associated syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1208614008",
        "display": "Autosomal dominant deafness with onychodystrophy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1208720000",
        "display": "Agenesis of corpus callosum, macrocephaly, hypertelorism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1208727002",
        "display": "Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1208746001",
        "display": "Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1208936008",
        "display": "Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1208987006",
        "display": "Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1217228004",
        "display": "X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1217229007",
        "display": "Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1217367007",
        "display": "Phospholipase A2 activating protein-associated neurodevelopmental disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1217371005",
        "display": "Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1217379007",
        "display": "NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1217381009",
        "display": "Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1217382002",
        "display": "Intellectual disability, autism, speech apraxia, craniofacial dysmorphism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1220568003",
        "display": "Glutamine rich 1-related intellectual disability, chondrodysplasia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1220589007",
        "display": "Keppen Lubinsky syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1220594007",
        "display": "Pierpont syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1220597000",
        "display": "Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1220600004",
        "display": "Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1222656005",
        "display": "Synaptic Ras GTPase activating protein 1-related developmental and epileptic encephalopathy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1222657001",
        "display": "Prune exopolyphosphatase 1-related neurological syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1222658006",
        "display": "Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1222659003",
        "display": "Ring finger protein 13-related severe early-onset epileptic encephalopathy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1222662000",
        "display": "Neonatal epileptic encephalopathy due to deficiency of glutaminase (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1222672002",
        "display": "3-methylglutaconic aciduria type 9 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1222706005",
        "display": "Anterior maxillary protrusion, strabismus, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1222710008",
        "display": "Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1228886008",
        "display": "9q33.3q34.11 microdeletion syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1228890005",
        "display": "16p13.2 microdeletion syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1229872004",
        "display": "Xq25 microduplication syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1229873009",
        "display": "17q24.2 microdeletion syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1229875002",
        "display": "9q21.13 microdeletion syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1229882003",
        "display": "11q22.2q22.3 microdeletion syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1229883008",
        "display": "19p13.3 microduplication syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1229891004",
        "display": "20q11.2 microdeletion syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1229895008",
        "display": "8q24.3 microdeletion syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1230273004",
        "display": "Megaconial congenital muscular dystrophy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1230376005",
        "display": "Contactin associated protein 2-related developmental and epileptic encephalopathy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1234774002",
        "display": "Cognitive impairment caused by ethanol (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "12348006",
        "display": "Presenile dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1236807002",
        "display": "Encephalopathy due to mitochondrial and peroxisomal fission defect (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1236843008",
        "display": "Phosphodiesterase 4D haploinsufficiency syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1237179007",
        "display": "FG syndrome type 1 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1237344003",
        "display": "Symptomatic form of fragile X syndrome in female carrier (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1237417007",
        "display": "Carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1237418002",
        "display": "Spastic tetraplegia, thin corpus callosum, progressive postnatal microcephaly syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1237420004",
        "display": "X-linked intellectual disability, global development delay, facial dysmorphism, sacral caudal remnant syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1237421000",
        "display": "Pyrroline-5-carboxylate reductase 2 related microcephaly, progressive leukoencephalopathy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1237462006",
        "display": "nudE neurodevelopment protein 1-related microhydranencephaly (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1237512003",
        "display": "Short stature, developmental delay, congenital heart defect syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1237619001",
        "display": "Fatty acyl-coenzyme A reductase 1 deficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1237623009",
        "display": "Congenital insensitivity to pain with severe intellectual disability (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1237625002",
        "display": "Autosomal recessive cerebellar ataxia due to CWF19 like cell cycle control factor 1 deficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1251452003",
        "display": "4q25 proximal deletion syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1251453008",
        "display": "Lamb Shaffer syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1254650002",
        "display": "Microcephaly, corpus callosum hypoplasia, intellectual disability, facial dysmorphism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1254651003",
        "display": "Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1254652005",
        "display": "Intellectual disability, macrocephaly, hypotonia, behavioral abnormalities syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1254654006",
        "display": "X-linked intellectual disability, hypotonia, movement disorder syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1255319004",
        "display": "Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1255322002",
        "display": "Congenital contracture of limbs and face, hypotonia, developmental delay syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1255335006",
        "display": "X-linked intellectual disability, short stature, overweight syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1258972007",
        "display": "Baraitser Winter cerebrofrontofacial syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259124000",
        "display": "Amyotrophic lateral sclerosis with frontotemporal dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259128002",
        "display": "Alzheimer disease with psychosis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259465009",
        "display": "Dementia due to hepatic failure (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259467001",
        "display": "Dementia due to hypercalcemia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259469003",
        "display": "Dementia due to Gerstmann Straussler Scheinker syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259471003",
        "display": "Dementia due to Hashimoto encephalopathy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259473000",
        "display": "Dementia due to fragile X syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259476008",
        "display": "Dementia due to genetic disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259478009",
        "display": "Dementia due to familial Creutzfeldt-Jakob disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259480003",
        "display": "Dementia due to fatal familial insomnia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259485008",
        "display": "Dementia due to cerebral vasculitis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259488005",
        "display": "Dementia due to cerebral amyloid angiopathy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259492003",
        "display": "Dementia due to metastatic malignant neoplasm to brain (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259494002",
        "display": "Dementia due to leukodystrophy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259496000",
        "display": "Dementia due to Lyme disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259499007",
        "display": "Dementia due to hemorrhagic cerebral infarction due to hypertension (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259501004",
        "display": "Dementia due to kuru (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259503001",
        "display": "Dementia due to iatrogenic Creutzfeldt-Jakob disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259511006",
        "display": "Dementia due to Wilson disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259513009",
        "display": "Dementia due to Whipple disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259517005",
        "display": "Dementia due to systemic lupus erythematosus (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259519008",
        "display": "Dementia due to subacute sclerosing panencephalitis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259522005",
        "display": "Dementia due to variant Creutzfeldt-Jakob disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259524006",
        "display": "Dementia due to trypanosomiasis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259529001",
        "display": "Dementia due to sporadic Creutzfeldt-Jakob disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259531005",
        "display": "Dementia due to hypertensive encephalopathy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259579003",
        "display": "Dementia due to Behcet syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259581001",
        "display": "Dementia due to celiac disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259584009",
        "display": "Dementia due to and following dialysis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259586006",
        "display": "Dementia due to autoimmune encephalitis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259591007",
        "display": "Dementia due to acquired hypothyroidism (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259656006",
        "display": "Dementia due to renal failure (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259661008",
        "display": "Dementia due to inflammatory disorder of musculoskeletal system (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259663006",
        "display": "Dementia due to polyarteritis nodosa (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259665004",
        "display": "Dementia due to progressive subcortical gliosis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259667007",
        "display": "Dementia due to paraneoplastic encephalitis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259673008",
        "display": "Dementia due to neurofilament inclusion body disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259675001",
        "display": "Dementia due to obstructive hydrocephalus (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259677009",
        "display": "Dementia due to multiple system atrophy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259679007",
        "display": "Dementia due to atypical pantothenate kinase associated neurodegeneration (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1259990004",
        "display": "Dementia due to classical pantothenate kinase associated neurodegeneration (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1260095004",
        "display": "Menke Hennekam syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1260097007",
        "display": "Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1260128008",
        "display": "Tryptophanyl tRNA synthetase 2, mitochondrial-related combined oxidative phosphorylation defect (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1260129000",
        "display": "Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1260130005",
        "display": "Progressive essential tremor, speech impairment, facial dysmorphism, intellectual disability, abnormal behavior syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1260134001",
        "display": "Spastic paraplegia, intellectual disability, nystagmus, obesity syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1260143005",
        "display": "Megalencephaly, severe kyphoscoliosis, overgrowth syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1260195002",
        "display": "Glutamate ionotropic receptor NMDA type subunit 2B-related developmental delay, intellectual disability, autism spectrum disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1260352009",
        "display": "Frontotemporal dementia due to TARDBP mutation (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1260353004",
        "display": "Frontotemporal dementia due to VCP mutation (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1260354005",
        "display": "Frontotemporal dementia due to C9orf72 mutation (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1260355006",
        "display": "Frontotemporal dementia due to FUS mutation (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1260449002",
        "display": "Polyendocrine polyneuropathy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1260450002",
        "display": "Infantile multisystem neurologic, endocrine, pancreatic disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1263555006",
        "display": "Logopenic non-amnestic Alzheimer disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1263585001",
        "display": "Frontal variant non-amnestic Alzheimer disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1269224009",
        "display": "Craniosynostosis, microretrognathia, severe intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1269226006",
        "display": "Spondylometaphyseal dysplasia, corneal dystrophy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1269233006",
        "display": "Posterior-predominant lissencephaly, broad flat pons and medulla-midline crossing defects syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1269236003",
        "display": "Primary hypomagnesemia, refractory seizures, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1275631007",
        "display": "Developmental and epileptic encephalopathy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1279845005",
        "display": "Combined oxidative phosphorylation defect type 39 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1284851009",
        "display": "Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "129104009",
        "display": "Developmental mental disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1295485009",
        "display": "Aldehyde dehydrogenase 18 family member A1-related de Barsy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1295488006",
        "display": "Pyrroline-5-carboxylate reductase 1 related de Barsy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1299154002",
        "display": "Cyclin dependent kinase 13-related congenital heart defects, intellectual disability, facial dysmorphism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1300119004",
        "display": "SET domain containing 2, histone lysine methyltransferase-related microcephaly, severe intellectual disability, multiple congenital anomalies syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1300131002",
        "display": "Neurexin 1-related severe neurodevelopmental disorder, motor stereotypies, chronic constipation, sleep-wake cycle disturbance (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1300132009",
        "display": "Clark Baraitser syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1300188000",
        "display": "Congenital pontocerebellar hypoplasia type 11 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1300192007",
        "display": "Congenital pontocerebellar hypoplasia type 14 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1300198006",
        "display": "SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily A, member 2-related blepharophimosis, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "130121000119104",
        "display": "Dementia due to Rett syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1303273003",
        "display": "Interferon regulatory factor 2 binding protein like-related regressive neurodevelopmental disorder, dystonia, seizures syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1303585005",
        "display": "Infantile neurodegeneration, progressive spasticity, intellectual disability, white matter lesions syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1303586006",
        "display": "Neurodevelopmental delay, hypotonia, cerebellar ataxia, cardiac conduction defects syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1303866001",
        "display": "Myelin transcription factor 1 like-related developmental delay, intellectual disability, obesity syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1304113005",
        "display": "Blepharophimosis, intellectual disability syndrome/genitopatellar overlap syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1304114004",
        "display": "Facial dysmorphism, hypertrichosis, epilepsy, intellectual disability/developmental delay, gingival overgrowth syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1304276001",
        "display": "Chromodomain helicase DNA binding protein 8 overgrowth syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1304277005",
        "display": "Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1.4 linker histone, cluster member mutation (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1332384001",
        "display": "Cyclin K-related neurodevelopmental disorder, severe intellectual disability, facial dysmorphism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1332385000",
        "display": "Aplastic anemia, intellectual disability, dwarfism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1332508004",
        "display": "Cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anemia, growth retardation syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1332510002",
        "display": "Chromodomain helicase DNA binding protein 4-related neurodevelopmental disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1335869007",
        "display": "Cleft palate, congenital heart defect, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1339031006",
        "display": "Dementia caused by ionizing radiation (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1340175001",
        "display": "Carboxypeptidase E-related Prader-Willi-like syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1340176000",
        "display": "Developmental delay, overweight, facial dysmorphism, behavioral abnormalities syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1351655009",
        "display": "Jansen-de Vries syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1351836007",
        "display": "Alkuraya Kucinskas syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1351837003",
        "display": "Intellectual disability, cupped ears syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1351838008",
        "display": "Intellectual disability, early-onset cataract, microcephaly syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1351843001",
        "display": "Lysine demethylase 3B-related intellectual disability, facial dysmorphism, short stature syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1351854006",
        "display": "Primary hypomagnesemia, generalized seizures, intellectual disability, obesity syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1351962002",
        "display": "Epidermal growth factor-related primary hypomagnesemia with intellectual disability (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1356735003",
        "display": "Oculogastrointestinal neurodevelopmental syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1356736002",
        "display": "Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual disability, Leber congenital amaurosis syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "14070001",
        "display": "Multi-infarct dementia with depression (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "141991000119109",
        "display": "Delusions in Alzheimer's disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "142001000119106",
        "display": "Depressed mood in Alzheimer's disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "142011000119109",
        "display": "Alzheimer's disease co-occurrent with delirium (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "15182000",
        "display": "Coffin-Lowry syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "15662003",
        "display": "Senile dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1581000119101",
        "display": "Dementia of the Alzheimer type with behavioral disturbance (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1591000119103",
        "display": "Dementia with behavioral disturbance (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "16219201000119101",
        "display": "Behavioral disturbance co-occurrent and due to late onset Alzheimer dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "162200009",
        "display": "Temporary loss of memory (finding)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "16276361000119109",
        "display": "Vascular dementia without behavioral disturbance (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "17827007",
        "display": "Cross syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "17961008",
        "display": "Conduct disorder, childhood-onset type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "18541000119100",
        "display": "Borderline cognitive developmental delay (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "1855002",
        "display": "Developmental academic disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "18941000",
        "display": "Oppositional defiant disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "191449005",
        "display": "Uncomplicated senile dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "191451009",
        "display": "Uncomplicated presenile dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "191452002",
        "display": "Presenile dementia with delirium (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "191454001",
        "display": "Presenile dementia with paranoia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "191455000",
        "display": "Presenile dementia with depression (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "191457008",
        "display": "Senile dementia with depressive or paranoid features (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "191458003",
        "display": "Senile dementia with paranoia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "191459006",
        "display": "Senile dementia with depression (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "191461002",
        "display": "Senile dementia with delirium (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "191463004",
        "display": "Uncomplicated arteriosclerotic dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "191464005",
        "display": "Arteriosclerotic dementia with delirium (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "191465006",
        "display": "Arteriosclerotic dementia with paranoia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "191466007",
        "display": "Arteriosclerotic dementia with depression (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "191493005",
        "display": "Dementia caused by drug (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "191519005",
        "display": "Dementia associated with another disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "191689008",
        "display": "Active infantile autism (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "191690004",
        "display": "Residual infantile autism (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "191692007",
        "display": "Active disintegrative psychoses (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "191693002",
        "display": "Residual disintegrative psychoses (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "192082001",
        "display": "Aggressive unsocial conduct disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "192092009",
        "display": "Group delinquency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "192099000",
        "display": "Childhood disorder of conduct and emotion (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "192100008",
        "display": "Neurotic delinquency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "192119003",
        "display": "Sibling jealousy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "192127007",
        "display": "Child attention deficit disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "192131001",
        "display": "Hyperkinesis with developmental delay (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "192132008",
        "display": "Hyperkinetic conduct disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "192136006",
        "display": "Specific reading disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "192138007",
        "display": "Developmental dyslexia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "192147004",
        "display": "Mixed disorder of psychological development (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "192562009",
        "display": "Disorder of psychological development (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "192575009",
        "display": "Mixed disorder of scholastic skills (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "192845009",
        "display": "Myoclonic encephalopathy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "21634003",
        "display": "Borjeson-Forssman-Lehmann syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "21921000119103",
        "display": "Dementia co-occurrent and due to Pick's disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "22381000119105",
        "display": "Primary degenerative dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "229676007",
        "display": "Language-related cognitive disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "229683000",
        "display": "Motor speech disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "229697008",
        "display": "Oral-verbal dyspraxia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "229698003",
        "display": "Articulatory dyspraxia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "229699006",
        "display": "Immature articulatory praxis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "229700007",
        "display": "Developmental motor speech disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "229701006",
        "display": "Developmental articulatory dyspraxia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "229703009",
        "display": "Developmental verbal dyspraxia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "229704003",
        "display": "Acquired choreiform dyspraxia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "229705002",
        "display": "Mixed acquired dyspraxia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "229706001",
        "display": "Ideomotor dyspraxia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "229707005",
        "display": "Dyspraxia of velopharynx (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "229708000",
        "display": "Velar dyspraxia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "229709008",
        "display": "Tongue tip dyspraxia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "229712006",
        "display": "Disorders of attention and motor control (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "229715008",
        "display": "Deficits in attention motor control and perception (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230191005",
        "display": "Rasmussen syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230265002",
        "display": "Familial Alzheimer's disease of early onset (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230266001",
        "display": "Non-familial Alzheimer's disease of early onset (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230267005",
        "display": "Familial Alzheimer's disease of late onset (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230268000",
        "display": "Non-familial Alzheimer's disease of late onset (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230269008",
        "display": "Focal Alzheimer's disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230270009",
        "display": "Frontotemporal dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230271008",
        "display": "Pick's disease with Pick bodies (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230272001",
        "display": "Pick's disease with Pick cells and no Pick bodies (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230274000",
        "display": "Frontal lobe degeneration with motor neurone disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230280008",
        "display": "Progressive aphasia in Alzheimer's disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230282000",
        "display": "Post-traumatic dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230285003",
        "display": "Vascular dementia of acute onset (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230286002",
        "display": "Subcortical vascular dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230287006",
        "display": "Mixed cortical and subcortical vascular dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230288001",
        "display": "Semantic dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230289009",
        "display": "Patchy dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230299004",
        "display": "Juvenile onset Huntington's disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230300007",
        "display": "Late onset Huntington's disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230301006",
        "display": "Akinetic-rigid form of Huntington's disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230418006",
        "display": "Lennox-Gastaut syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230419003",
        "display": "Cryptogenic Lennox-Gastaut syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230420009",
        "display": "Symptomatic Lennox-Gastaut syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230421008",
        "display": "Epilepsy with myoclonic-atonic seizures (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230429005",
        "display": "Early infantile epileptic encephalopathy with suppression bursts (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230437002",
        "display": "Severe myoclonic epilepsy in infancy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230439004",
        "display": "Epilepsy with continuous spike wave during slow-wave sleep (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230736007",
        "display": "Transient global amnesia (finding)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "230782004",
        "display": "Dysequilibrium syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "2312009",
        "display": "Reactive attachment disorder of infancy OR early childhood, inhibited type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "23148009",
        "display": "Undifferentiated attention deficit disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "231536004",
        "display": "Atypical autism (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "231537008",
        "display": "Developmental agnosia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "231540008",
        "display": "Conduct disorder - in family context (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "231541007",
        "display": "Conduct disorder - unsocialized (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "231542000",
        "display": "Depressive conduct disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "232059000",
        "display": "Laurence-Moon syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "234146006",
        "display": "Hennekam lymphangiectasia-lymphedema syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "23560001",
        "display": "Asperger's disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "236529001",
        "display": "Prune belly syndrome with pulmonic stenosis, intellectual disability and deafness (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "24125008",
        "display": "Mental disorder in infancy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "2421000119107",
        "display": "Hallucinations co-occurrent and due to late onset dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "247607004",
        "display": "Amnesia for day to day facts (finding)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "247611005",
        "display": "Amnesia for important personal information (finding)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "253176002",
        "display": "Gillespie syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "25772007",
        "display": "Multi-infarct dementia with delusions (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "26453000",
        "display": "Mental disorder in adolescence (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "26852004",
        "display": "Primary degenerative dementia of the Alzheimer type, senile onset, with depression (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "268612007",
        "display": "Senile and presenile organic psychotic conditions (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "268661009",
        "display": "Nonaggressive unsocial conduct disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "268662002",
        "display": "Unsocial childhood truancy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "268674003",
        "display": "Developmental disorder of motor function (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "268738002",
        "display": "Specific spelling disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "26929004",
        "display": "Alzheimer's disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "270905000",
        "display": "Childhood disinhibited attachment disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "275271004",
        "display": "Apraxia, developmental (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "275277000",
        "display": "Post-traumatic amnesia (finding)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "27544004",
        "display": "Developmental coordination disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "278857002",
        "display": "Dementia of frontal lobe type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "278920007",
        "display": "Speech and language dyspraxias (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "281004",
        "display": "Dementia associated with alcoholism (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "288631000119104",
        "display": "Vascular dementia with behavioral disturbance (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "290621000119101",
        "display": "Cognitive deficit due to and following cerebrovascular disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "291621000119109",
        "display": "Cognitive deficit due to and following nontraumatic subarachnoid hemorrhage (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "291711000119109",
        "display": "Cognitive deficit due to and following nontraumatic intracerebral hemorrhage (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "293671000119109",
        "display": "Behavioral disturbance due to multi-infarct dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "30509009",
        "display": "Gender identity disorder of adolescence, previously homosexual (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "307653008",
        "display": "Clumsiness - motor delay (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "31081000119101",
        "display": "Presenile dementia with delusions (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "31177006",
        "display": "Attention deficit hyperactivity disorder, combined type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "31216003",
        "display": "Profound intellectual disability (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "312991009",
        "display": "Senile dementia of the Lewy body type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "31648009",
        "display": "Unaggressive type unsocialized behavior disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "32875003",
        "display": "Inhalant-induced persisting dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "33982008",
        "display": "Hyperphosphatasemia with intellectual disability (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "35253001",
        "display": "Attention deficit hyperactivity disorder, predominantly inattentive type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "35919005",
        "display": "Pervasive developmental disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "359661001",
        "display": "Specific number difficulty (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "361275004",
        "display": "Oral dyspraxia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "361277007",
        "display": "Verbal dyspraxia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "363236004",
        "display": "Neurodevelopmental disorder of fetus (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "371024007",
        "display": "Senile dementia with delusion (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "371026009",
        "display": "Senile dementia with psychosis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "373618009",
        "display": "Autistic spectrum disorder with isolated skills (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "386805003",
        "display": "Mild neurocognitive disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "386820009",
        "display": "Socialized behavior disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "3914008",
        "display": "Mental disorder in childhood (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "395689002",
        "display": "Transient epileptic amnesia (finding)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "39951000119105",
        "display": "Pervasive developmental disorder of residual state (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "40083003",
        "display": "Stereotypic movement disorder with self-injurious behavior (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "406506008",
        "display": "Attention deficit hyperactivity disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "40700009",
        "display": "Severe intellectual disability (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "408857007",
        "display": "Infantile autism (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "412787009",
        "display": "Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "41526007",
        "display": "Reactive attachment disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "416780008",
        "display": "Primary degenerative dementia of the Alzheimer type, presenile onset (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "416975007",
        "display": "Primary degenerative dementia of the Alzheimer type, senile onset (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "420614009",
        "display": "Organic dementia with acquired immunodeficiency syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "421023003",
        "display": "Presenile dementia with acquired immunodeficiency syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "421529006",
        "display": "Dementia with acquired immunodeficiency syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "42176003",
        "display": "Amnesia for recent events (finding)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "422437002",
        "display": "X-linked intellectual disability with marfanoid habitus (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "425390006",
        "display": "Dementia associated with Parkinson's Disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "425805004",
        "display": "Cognitive developmental delay (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "428051000124108",
        "display": "Mild dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "428351000124105",
        "display": "Severe dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "429161000124103",
        "display": "Primary degenerative dementia of the Alzheimer type, senile onset, with behavioral disturbance (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "429458009",
        "display": "Dementia due to Creutzfeldt Jakob disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "429998004",
        "display": "Vascular dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "430099007",
        "display": "Gross motor development delay (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "430771000124100",
        "display": "Moderate dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "430909002",
        "display": "Conduct disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "431111000124104",
        "display": "Lennox-Gastaut syndrome, refractory (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "431121000124107",
        "display": "Lennox-Gastaut syndrome, non-refractory (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "432091002",
        "display": "Savant syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "433081000",
        "display": "Organic amnesia of language (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "435341000124104",
        "display": "Rasmussen syndrome, refractory (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "43614003",
        "display": "Autistic disorder of childhood onset (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "44124003",
        "display": "Reactive attachment disorder of early childhood (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "442168001",
        "display": "Retardation of physical development (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "442212003",
        "display": "Residual cognitive deficit as late effect of cerebrovascular accident (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "442314000",
        "display": "Active but odd autism (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "442344002",
        "display": "Dementia due to Huntington chorea (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "443265004",
        "display": "Cognitive disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "443735008",
        "display": "Nonverbal learning disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "44423001",
        "display": "Early myoclonic encephalopathy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "444613000",
        "display": "Adult attention deficit hyperactivity disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "45677003",
        "display": "Developmental expressive writing disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "47916000",
        "display": "Developmental arithmetic disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "48167000",
        "display": "Amnesia (finding)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "4817008",
        "display": "Primary degenerative dementia of the Alzheimer type, senile onset, with delirium (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "48826008",
        "display": "Conduct disorder, adolescent-onset type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "4949009",
        "display": "Motor skill disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "51921000",
        "display": "Retrograde amnesia (finding)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "51928006",
        "display": "General paresis - neurosyphilis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "52448006",
        "display": "Dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "52824009",
        "display": "Developmental reading disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "54319003",
        "display": "Disruptive behavior disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "54502004",
        "display": "Primary degenerative dementia of the Alzheimer type, presenile onset, with delusions (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "55009008",
        "display": "Primary degenerative dementia of the Alzheimer type, senile onset, with delusions (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "5507002",
        "display": "Stereotypy habit disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "5619004",
        "display": "Bardet-Biedl syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "56267009",
        "display": "Multi-infarct dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "57715001",
        "display": "Gender identity disorder of adolescence (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "57917004",
        "display": "Seckel syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "58756001",
        "display": "Huntington's chorea (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "59252009",
        "display": "de Barsey syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "59651006",
        "display": "Sedative, hypnotic AND/OR anxiolytic-induced persisting dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "61152003",
        "display": "Moderate intellectual disability (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "613003",
        "display": "Fragile X syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "6149008",
        "display": "Amnesia for remote events (finding)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "61901004",
        "display": "Conduct disorder, undifferentiated type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "6475002",
        "display": "Primary degenerative dementia of the Alzheimer type, presenile onset, uncomplicated (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "65096006",
        "display": "Primary degenerative dementia of the Alzheimer type, presenile onset, with delirium (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "66108005",
        "display": "Primary degenerative dementia of the Alzheimer type, senile onset, uncomplicated (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "66307007",
        "display": "Conduct disorder, group type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "672561000119103",
        "display": "Cognitive deficit due to and following ischemic cerebrovascular accident (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "672571000119109",
        "display": "Cognitive deficit due to and following hemorrhagic cerebrovascular accident (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "68618008",
        "display": "Rett syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "68963006",
        "display": "Gender identity disorder of adolescence, previously heterosexual (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "690341000119100",
        "display": "Cognitive deficit due to and following embolic cerebrovascular accident (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "698624003",
        "display": "Dementia associated with cerebral lipidosis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "698625002",
        "display": "Dementia associated with normal pressure hydrocephalus (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "698626001",
        "display": "Dementia associated with multiple sclerosis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "698687007",
        "display": "Post-traumatic dementia with behavioral change (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "698689005",
        "display": "Attention deficit hyperactivity disorder, predominantly inattentive type in remission (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "698691002",
        "display": "Cognitive disorder in remission (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "698692009",
        "display": "Attention deficit hyperactivity disorder, predominantly hyperactive impulsive type in remission (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "698725008",
        "display": "Dementia associated with neurosyphilis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "698726009",
        "display": "Dementia associated with viral encephalitis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "698781002",
        "display": "Dementia associated with cerebral anoxia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "698947004",
        "display": "Conduct disorder in remission (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "698948009",
        "display": "Vascular dementia in remission (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "698949001",
        "display": "Dementia in remission (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "698954005",
        "display": "Primary degenerative dementia of the Alzheimer type, senile onset in remission (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "698955006",
        "display": "Primary degenerative dementia of the Alzheimer type, presenile onset in remission (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "699297004",
        "display": "Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "699298009",
        "display": "Blepharophimosis, intellectual disability syndrome, Say-Barber-Biesecker-Young-Simpson type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "699316006",
        "display": "Myhre syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "699669001",
        "display": "Renpenning syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "700364009",
        "display": "Neurodevelopmental disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "702327009",
        "display": "Monocarboxylate transporter 8 deficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "702344008",
        "display": "Pitt-Hopkins syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "702354007",
        "display": "X-linked intellectual developmental disorder Christianson type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "702356009",
        "display": "X-linked intellectual disability-psychosis-macroorchidism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "702393003",
        "display": "Frontotemporal dementia with gene located on 3p11 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "702412005",
        "display": "X-linked intellectual deficit-dystonia-dysarthria syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "702416008",
        "display": "X-linked intellectual disability Snyder type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "702423009",
        "display": "Deafness-dystonia-optic neuronopathy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "702441001",
        "display": "Fatal X-linked ataxia with deafness and loss of vision (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "702450004",
        "display": "FOXG1 syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "702732007",
        "display": "High-functioning autism (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "702815001",
        "display": "Attention deficit hyperactivity disorder, inattentive presentation (restrictive) (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "703389002",
        "display": "Calcium/calmodulin-dependent serine protein kinase related intellectual disability (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "703477003",
        "display": "Developmental delay in fine motor function (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "703526007",
        "display": "Progressive epilepsy-intellectual disability syndrome Finnish type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "703535000",
        "display": "Mowat-Wilson syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "708037001",
        "display": "Residual Asperger's disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "709073001",
        "display": "Neurocognitive disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "70936005",
        "display": "Multi-infarct dementia, uncomplicated (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "712884004",
        "display": "Pathological demand avoidance (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "713488003",
        "display": "Presenile dementia co-occurrent with human immunodeficiency virus infection (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "713844000",
        "display": "Dementia co-occurrent with human immunodeficiency virus infection (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "715409005",
        "display": "Trigonocephaly C syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "715428003",
        "display": "Skeletal dysplasia with epilepsy and short stature syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "715441004",
        "display": "McDonough syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "715628009",
        "display": "Intellectual disability, truncal obesity, retinal dystrophy and micropenis syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "715737004",
        "display": "Parkinsonism co-occurrent with dementia of Guadeloupe (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "715989002",
        "display": "Congenital cataract with intellectual disability and anal atresia and urinary defect syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "716024001",
        "display": "Goniodysgenesis with intellectual disability and short stature syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "716089008",
        "display": "Craniofacial digital and genital anomalies syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "716096005",
        "display": "Hypospadias and intellectual disability syndrome Goldblatt type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "716107009",
        "display": "Early onset parkinsonism and intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "716112005",
        "display": "Microcephaly with deafness and intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "716191002",
        "display": "Alopecia and intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "716334004",
        "display": "Intellectual disability and short stature with hand contracture and genital anomaly syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "716667005",
        "display": "Right temporal atrophy variant frontotemporal dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "716706009",
        "display": "Female restricted epilepsy with intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "716709002",
        "display": "FRAXE intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "716994006",
        "display": "Behavioral variant of frontotemporal dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "716996008",
        "display": "Hypoplasia of corpus callosum, intellectual disability, adducted thumbs, spasticity, hydrocephalus syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "717157006",
        "display": "Trisomy 10p (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "717222003",
        "display": "Microphthalmia with ankyloblepharon and intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "717223008",
        "display": "X-linked epilepsy with learning disability and behavior disorder syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "717276003",
        "display": "Folinic acid responsive seizure syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "717822006",
        "display": "Goldberg Shprintzen megacolon syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "717887003",
        "display": "Biemond syndrome type 2 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "717913006",
        "display": "Blepharonasofacial malformation syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "717945001",
        "display": "Brain anomaly, severe intellectual disability, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "718226002",
        "display": "Wolf Hirschhorn syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "718393002",
        "display": "Atypical Rett syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "718573009",
        "display": "Achalasia microcephaly syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "718577005",
        "display": "X-linked intellectual disability Atkin type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "718680001",
        "display": "Oro-facial digital syndrome type 9 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "718681002",
        "display": "Oro-facial digital syndrome type 11 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "718766002",
        "display": "Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "718845002",
        "display": "X-linked intellectual disability with ataxia and apraxia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "718847005",
        "display": "X-linked neurodegenerative syndrome Hamel type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "718848000",
        "display": "Fried syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "718896000",
        "display": "X-linked recessive intellectual disability and macrocephaly with ciliary dysfunction syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "718897009",
        "display": "X-linked intellectual disability Seemanova type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "718900002",
        "display": "Syndromic X-linked intellectual disability type 11 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "718905007",
        "display": "X-linked intellectual disability Shrimpton type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "718908009",
        "display": "X-linked intellectual disability Siderius type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "718909001",
        "display": "X-linked intellectual disability Stevenson type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "718910006",
        "display": "X-linked intellectual disability Stocco Dos Santos type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "718911005",
        "display": "X-linked intellectual disability Stoll type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "718912003",
        "display": "X-linked intellectual disability Turner type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "718914002",
        "display": "X-linked intellectual disability Van Esch type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719009006",
        "display": "X-linked intellectual disability Wilson type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719010001",
        "display": "X-linked intellectual disability Schimke type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719011002",
        "display": "X-linked intellectual disability Pai type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719012009",
        "display": "X-linked intellectual disability Miles Carpenter type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719013004",
        "display": "X-linked intellectual disability Cilliers type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719016007",
        "display": "X-linked intellectual disability Cantagrel type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719017003",
        "display": "X-linked intellectual disability Armfield type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719018008",
        "display": "X-linked intellectual disability Abidi type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719020006",
        "display": "Pallister W syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719042007",
        "display": "Uveal coloboma with cleft lip and palate and intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719046005",
        "display": "12q14 microdeletion syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719069008",
        "display": "Shprintzen Goldberg craniosynostosis syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719097002",
        "display": "Branchioskeletogenital syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719102004",
        "display": "Congenital cataract with ataxia and deafness syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719136005",
        "display": "X-linked intellectual disability with cerebellar hypoplasia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719138006",
        "display": "X-linked intellectual disability with cubitus valgus and dysmorphism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719139003",
        "display": "X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizure syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719140001",
        "display": "X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719155005",
        "display": "X-linked intellectual disability and epilepsy with progressive joint contracture and facial dysmorphism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719156006",
        "display": "X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719157002",
        "display": "X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719160009",
        "display": "Syndromic X-linked intellectual disability type 7 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719161008",
        "display": "Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719162001",
        "display": "Radioulnar synostosis with microcephaly and scoliosis syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719202006",
        "display": "Spondyloepiphyseal dysplasia tarda Kohn type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719378009",
        "display": "Microcephalus with brachydactyly and kyphoscoliosis syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719380003",
        "display": "Microcephalus cardiomyopathy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719450007",
        "display": "Disorder of sex development with intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719466009",
        "display": "Cleft palate with short stature and vertebral anomaly syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719583002",
        "display": "17q11.2 microduplication syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719599008",
        "display": "19q13.11 microdeletion syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719600006",
        "display": "1p21.3 microdeletion syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "71961003",
        "display": "Childhood disintegrative disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719800009",
        "display": "Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719808002",
        "display": "Chromosome Xp11.3 microdeletion syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719810000",
        "display": "X-linked intellectual disability with seizure and psoriasis syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719811001",
        "display": "X-linked intellectual disability Cabezas type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719812008",
        "display": "X-linked intellectual disability with plagiocephaly syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719825000",
        "display": "X-linked intellectual disability, macrocephaly, macroorchidism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719826004",
        "display": "X-linked intellectual disability with acromegaly and hyperactivity syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719834005",
        "display": "Wilson Turner syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719842006",
        "display": "Congenital hypoplasia of ulna and intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "719947004",
        "display": "Craniofacial dysmorphism with coloboma of eye and corpus callosum agenesis syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "720010009",
        "display": "Microphthalmia with brain atrophy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "720401009",
        "display": "Cystic fibrosis with gastritis and megaloblastic anemia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "720468000",
        "display": "Aniridia and intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "720501007",
        "display": "Arachnodactyly with abnormal ossification and intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "720502000",
        "display": "Arachnodactyly and intellectual disability with facial dysmorphism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "720517001",
        "display": "Ataxia with deafness and intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "720573009",
        "display": "Brachymorphism with onychodysplasia and dysphalangism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "720635002",
        "display": "Cerebro-facio-thoracic dysplasia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "720639008",
        "display": "Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "720746006",
        "display": "Contracture with ectodermal dysplasia and orofacial cleft syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "720748007",
        "display": "Aural atresia with multiple congenital anomalies and intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "720825005",
        "display": "Cystic leukoencephalopathy without megalencephaly (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "720855003",
        "display": "Cerebrooculonasal syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "720954000",
        "display": "Filippi syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "720955004",
        "display": "Fine Lubinsky syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "720957007",
        "display": "Deafness with skeletal dysplasia and lip granuloma syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "720979002",
        "display": "Alopecia, contracture, dwarfism, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "720981000",
        "display": "Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "720982007",
        "display": "Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "721007005",
        "display": "Hair defect with photosensitivity and intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "721008000",
        "display": "Hall Riggs syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "721017000",
        "display": "Postaxial polydactyly and intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "721073008",
        "display": "Short stature with webbed neck and congenital heart disease syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "721086004",
        "display": "Deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "721087008",
        "display": "Deafness and intellectual disability Martin Probst type syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "721089006",
        "display": "Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "721146009",
        "display": "Intellectual disability, epilepsy, bulbous nose syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "721207002",
        "display": "Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "721208007",
        "display": "Ectodermal dysplasia with blindness syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "721251000124100",
        "display": "Early infantile developmental and epileptic encephalopathy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "721841001",
        "display": "Hypogonadism with mitral valve prolapse and intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "721843003",
        "display": "Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "721875000",
        "display": "Juberg Marsidi syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "721883006",
        "display": "Radioulnar synostosis with developmental delay and hypotonia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "721973006",
        "display": "Lipodystrophy, intellectual disability, deafness syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "721974000",
        "display": "Lowry MacLean syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722002002",
        "display": "Intellectual disability, balding, patella luxation, acromicria syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722031003",
        "display": "Kapur Toriello syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722033000",
        "display": "Macrocephaly, short stature, paraplegia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722035007",
        "display": "Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722037004",
        "display": "Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722055008",
        "display": "Oculopalatocerebral syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722056009",
        "display": "Oculocerebrofacial syndrome Kaufman type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722075004",
        "display": "Oro-facial digital syndrome type 10 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722105002",
        "display": "Oro-facial digital syndrome type 5 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722106001",
        "display": "Oro-facial digital syndrome type 8 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722107005",
        "display": "Ossification anomaly with psychomotor developmental delay syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722110003",
        "display": "Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722209002",
        "display": "Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722213009",
        "display": "Severe X-linked intellectual disability Gustavson type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722281001",
        "display": "Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722282008",
        "display": "Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722378009",
        "display": "Congenital cataract with deafness and hypogonadism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722379001",
        "display": "Congenital cataract with hypertrichosis and intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722380003",
        "display": "Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722454003",
        "display": "Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722455002",
        "display": "Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722456001",
        "display": "Intellectual disability, developmental delay, contracture syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722459008",
        "display": "Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722477003",
        "display": "Toriello Carey syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722478008",
        "display": "Skeletal dysplasia with intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722600006",
        "display": "Non-amnestic Alzheimer disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722975002",
        "display": "Primary stereotypy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722976001",
        "display": "Secondary stereotypy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722977005",
        "display": "Dementia co-occurrent and due to neurocysticercosis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722978000",
        "display": "Toxic dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722979008",
        "display": "Dementia due to metabolic abnormality (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "722980006",
        "display": "Dementia due to chromosomal anomaly (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "723123001",
        "display": "Ischemic vascular dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "723125008",
        "display": "Epileptic encephalopathy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "723304001",
        "display": "Microcephaly, seizure, intellectual disability, heart disease syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "723332005",
        "display": "Isodicentric chromosome 15 syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "723333000",
        "display": "Faciocardiorenal syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "723336008",
        "display": "Fallot complex with intellectual disability and growth delay syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "723365002",
        "display": "Hypotrichosis and intellectual disability syndrome Lopes type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "723390000",
        "display": "Rapidly progressive dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "723403008",
        "display": "Microbrachycephaly, ptosis, cleft lip syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "723410002",
        "display": "N syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "723441001",
        "display": "Non-progressive cerebellar ataxia with intellectual disability (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "723454008",
        "display": "Phosphoribosylpyrophosphate synthetase superactivity (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "723504000",
        "display": "Ramos Arroyo syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "723621000",
        "display": "Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "723676007",
        "display": "Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "723994004",
        "display": "Seizures and intellectual disability due to hydroxylysinuria syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "724001005",
        "display": "Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "724039002",
        "display": "Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "724137002",
        "display": "Macrocephaly, obesity, mental disability, ocular abnormality syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "724178000",
        "display": "Laryngeal abductor paralysis with intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "724207001",
        "display": "Kleefstra syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "724228005",
        "display": "Infantile choroidocerebral calcification syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "724652008",
        "display": "Stereotypic movement disorder without self-injurious behavior (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "724733005",
        "display": "Oppositional defiant disorder co-occurrent with chronic irritability-anger (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "724734004",
        "display": "Oppositional defiant disorder co-occurrent with chronic irritability-anger with normal prosocial emotions (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "724735003",
        "display": "Oppositional defiant disorder without chronic irritability-anger (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "724736002",
        "display": "Oppositional defiant disorder without chronic irritability-anger with limited prosocial emotions (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "724737006",
        "display": "Oppositional defiant disorder without chronic irritability-anger with normal prosocial emotions (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "724738001",
        "display": "Childhood onset conduct-dissocial disorder with limited prosocial emotions (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "724739009",
        "display": "Childhood onset conduct-dissocial disorder with normal prosocial emotions (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "724740006",
        "display": "Adolescent onset conduct-dissocial disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "724741005",
        "display": "Adolescent onset conduct-dissocial disorder with limited prosocial emotions (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "724742003",
        "display": "Adolescent onset conduct-dissocial disorder with normal prosocial emotions (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "724776007",
        "display": "Dementia due to disorder of central nervous system (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "724777003",
        "display": "Dementia due to infectious disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "724992007",
        "display": "Epilepsy co-occurrent and due to dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "725140007",
        "display": "Temple Baraitser syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "725163002",
        "display": "X-linked spasticity, intellectual disability, epilepsy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "725289009",
        "display": "5-amino-4-imidazole carboxamide ribosiduria (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "725413002",
        "display": "Febrile infection related epilepsy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "725589005",
        "display": "Bullous dystrophy macular type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "725898002",
        "display": "Delirium co-occurrent with dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "725906006",
        "display": "Intellectual disability Buenos Aires type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "725908007",
        "display": "Neurofaciodigitorenal syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "725912001",
        "display": "X-linked intellectual disability Brooks type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "726031001",
        "display": "Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "726621009",
        "display": "Caudal appendage deafness syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "726669007",
        "display": "Central nervous system calcification, deafness, tubular acidosis, anemia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "726670008",
        "display": "Weaver Williams syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "726672000",
        "display": "Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "726702005",
        "display": "Epileptic encephalopathy with global cerebral demyelination (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "726709001",
        "display": "Intellectual disability, cataract, calcified pinna, myopathy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "726727003",
        "display": "X-linked intellectual disability Hedera type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "726732002",
        "display": "X-linked intellectual disability Nascimento type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "7291006",
        "display": "Reactive attachment disorder of infancy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "732246009",
        "display": "X-linked intellectual disability, limb spasticity, retinal dystrophy, arginine vasopressin deficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "732251003",
        "display": "Cortical blindness, intellectual disability, polydactyly syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "732954002",
        "display": "Osteopenia, intellectual disability, sparse hair syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "732957009",
        "display": "Brachydactyly and preaxial hallux varus syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "732958004",
        "display": "Spastic paraplegia with precocious puberty syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "732961003",
        "display": "Branchial dysplasia, intellectual disability, inguinal hernia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733031004",
        "display": "Epilepsy, microcephaly, skeletal dysplasia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733032006",
        "display": "Epilepsy telangiectasia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733049004",
        "display": "Encephalopathy, intracerebral calcification, retinal degeneration syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733050004",
        "display": "Dysmorphism, short stature, deafness, disorder of sex development syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733062000",
        "display": "Marfanoid habitus with autosomal recessive intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733072002",
        "display": "Alaninuria, microcephaly, dwarfism, enamel hypoplasia, diabetes mellitus syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733086003",
        "display": "Pseudoprogeria syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733088002",
        "display": "Preaxial polydactyly, colobomata, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733097003",
        "display": "Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733110004",
        "display": "Van den Bosch syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733116005",
        "display": "Aniridia, renal agenesis, psychomotor retardation syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733117001",
        "display": "Thumb stiffness, brachydactyly, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733184002",
        "display": "Dementia caused by heavy metal exposure (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733190003",
        "display": "Dementia due to primary malignant neoplasm of brain (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733191004",
        "display": "Dementia due to chronic subdural hematoma (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733192006",
        "display": "Dementia due to herpes encephalitis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733193001",
        "display": "Dementia co-occurrent and due to progressive multifocal leukoencephalopathy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733194007",
        "display": "Dementia co-occurrent and due to Down syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733417008",
        "display": "Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733419006",
        "display": "Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733455003",
        "display": "Spastic paraplegia, glaucoma, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733472005",
        "display": "Microcephalus, glomerulonephritis, marfanoid habitus syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733522005",
        "display": "Megalocornea with intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "733623005",
        "display": "Autism spectrum disorder, epilepsy, arthrogryposis syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "734017008",
        "display": "Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "734173003",
        "display": "Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "734349003",
        "display": "Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "737343009",
        "display": "Secondary neurodevelopmental disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "7461003",
        "display": "Attention deficit hyperactivity disorder, predominantly hyperactive impulsive type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "74850006",
        "display": "Conduct disorder, solitary aggressive type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "762298000",
        "display": "Cognitive impairment due to toxicity of substance (finding)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "762347009",
        "display": "Childhood onset conduct-dissocial disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "762350007",
        "display": "Dementia due to prion disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "762351006",
        "display": "Dementia due to and following injury of head (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "762707000",
        "display": "Subcortical dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763136000",
        "display": "Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763186006",
        "display": "Grubben, De Cock, Borghgraef syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763278004",
        "display": "Facial dysmorphism, cleft palate, loose skin syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763320005",
        "display": "Craniofaciofrontodigital syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763344007",
        "display": "Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763350002",
        "display": "Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763353000",
        "display": "Cerebrofacioarticular syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763404001",
        "display": "Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763615003",
        "display": "Aortic arch anomaly, facial dysmorphism, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763618001",
        "display": "Wiedemann Steiner syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763626009",
        "display": "Intellectual disability due to nutritional deficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763665007",
        "display": "Craniodigital syndrome and intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763722004",
        "display": "Hypotonia, speech impairment, severe cognitive delay syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763741001",
        "display": "Intellectual disability, alacrima, achalasia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763742008",
        "display": "Intellectual disability, polydactyly, uncombable hair syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763743003",
        "display": "Intellectual disability, spasticity, ectrodactyly syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763744009",
        "display": "Intellectual disability, brachydactyly, Pierre Robin syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763745005",
        "display": "Intellectual disability Wolff type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763773007",
        "display": "Macrocephaly and developmental delay syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763795006",
        "display": "Malan overgrowth syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763797003",
        "display": "Agenesis of corpus callosum and abnormal genitalia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763837007",
        "display": "Oro-facial digital syndrome type 14 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "763861000",
        "display": "Pachygyria, intellectual disability, epilepsy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "764455002",
        "display": "Cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, skeletal dysplasia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "764732004",
        "display": "Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "764861005",
        "display": "Intellectual disability Birk-Barel type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "764950001",
        "display": "Cryptorchidism, arachnodactyly, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "764959000",
        "display": "Intellectual disability, myopathy, short stature, endocrine defect syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "765089003",
        "display": "Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "765093009",
        "display": "Rolandic epilepsy, speech dyspraxia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "765170001",
        "display": "Sodium voltage-gated channel alpha subunit 8-related epilepsy with encephalopathy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "765325002",
        "display": "Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "765434008",
        "display": "Human immunodeficiency virus type I enhancer binding protein 2 related intellectual disability (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "765471005",
        "display": "X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "765758008",
        "display": "Microcephalic primordial dwarfism Montreal type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "765761009",
        "display": "Brachydactyly, mesomelia, intellectual disability, heart defect syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "766753005",
        "display": "Nijmegen breakage syndrome-like disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "766824003",
        "display": "Activity dependent neuroprotector homeobox related multiple congenital anomalies, intellectual disability, autism spectrum disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "766870005",
        "display": "Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "766871009",
        "display": "Diencephalic mesencephalic junction dysplasia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "766932005",
        "display": "Hypothalamic hamartoma with gelastic seizure (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "768473009",
        "display": "Purine rich element binding protein A syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "768555009",
        "display": "5q31.3 microdeletion syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "768666006",
        "display": "Syntaxin binding protein 1 encephalopathy with epilepsy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "768677000",
        "display": "Protein phosphatase 2 regulatory subunit b (b56) delta-related intellectual disability (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "76880004",
        "display": "Angelman syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "768843007",
        "display": "Tall stature, intellectual disability, facial dysmorphism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "770404004",
        "display": "Autosomal recessive chorioretinopathy and microcephaly syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "770431001",
        "display": "Early-onset epileptic encephalopathy and intellectual disability due to glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A mutation (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "770564004",
        "display": "Microcephalic primordial dwarfism Alazami type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "770565003",
        "display": "Microcephalic primordial dwarfism Dauber type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "770604006",
        "display": "X-linked cerebral, cerebellar, coloboma syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "770679002",
        "display": "Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "770719004",
        "display": "3q27.3 microdeletion syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "770721009",
        "display": "Microcephaly, thin corpus callosum, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "770723007",
        "display": "Optic atrophy, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "770725000",
        "display": "Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "770750002",
        "display": "Intellectual disability, seizures, macrocephaly, obesity syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "770751003",
        "display": "Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "770755007",
        "display": "Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "770756008",
        "display": "2p13.2 microdeletion syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "770790004",
        "display": "Developmental delay with autism spectrum disorder and gait instability (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "770793002",
        "display": "5p13 microduplication syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "770794008",
        "display": "11p15.4 microduplication syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "770898002",
        "display": "Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "770901001",
        "display": "Autosomal recessive intellectual disability, motor dysfunction, multiple joint contracture syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "770907002",
        "display": "Kagami Ogata syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "770941005",
        "display": "Alopecia, progressive neurological defect, endocrinopathy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "771074000",
        "display": "Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "771077007",
        "display": "Intellectual disability, short stature, hypertelorism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "771148008",
        "display": "X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "771149000",
        "display": "Hepatic fibrosis, renal cyst, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "771179007",
        "display": "Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "771223000",
        "display": "Infantile epileptic dyskinetic encephalopathy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "771262009",
        "display": "Pseudoleprechaunism syndrome Patterson type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "771303004",
        "display": "Severe neonatal onset encephalopathy with microcephaly (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "771336003",
        "display": "Polymicrogyria with optic nerve hypoplasia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "771448004",
        "display": "Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "771470001",
        "display": "Jawad syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "771472009",
        "display": "Developmental and speech delay due to SRY-box 5 deficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "771476007",
        "display": "Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "771477003",
        "display": "15q overgrowth syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "771512003",
        "display": "Autism spectrum disorder due to AUTS2 activator of transcription and developmental regulator deficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "771516000",
        "display": "Solute carrier family 35 member A2 congenital disorder of glycosylation (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "772127009",
        "display": "White Sutton syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "772224009",
        "display": "Warburg micro syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "772225005",
        "display": "RAB18, member RAS oncogene family deficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "77287004",
        "display": "Borderline intellectual disability (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773230003",
        "display": "Cyclin-dependent kinase-like 5 deficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773274001",
        "display": "X-linked intellectual disability, craniofacioskeletal syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773303005",
        "display": "Spondyloepimetaphyseal dysplasia Genevieve type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773307006",
        "display": "Zechi Ceide syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773329005",
        "display": "CK syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773400009",
        "display": "Severe feeding difficulties, failure to thrive, microcephaly due to ASXL transcriptional regulator 3 deficiency syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773404000",
        "display": "Roifman syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773405004",
        "display": "Intellectual disability with strabismus syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773416006",
        "display": "Intellectual disability, facial dysmorphism, hand anomalies syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773418007",
        "display": "Xylosyltransferase 1 congenital disorder of glycosylation (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773419004",
        "display": "Severe intellectual disability, short stature, behavioral abnormalities, facial dysmorphism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773421009",
        "display": "Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773493002",
        "display": "9q31.1q31.3 microdeletion syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773494008",
        "display": "14q24.1q24.3 microdeletion syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773498006",
        "display": "Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773547003",
        "display": "13q12.3 microdeletion syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773548008",
        "display": "Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773551001",
        "display": "Severe intellectual disability, poor language, strabismus, grimacing face, long fingers syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773552008",
        "display": "Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773553003",
        "display": "Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773554009",
        "display": "THO complex 6-related developmental delay, microcephaly, facial dysmorphism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773556006",
        "display": "Short ulna, dysmorphism, hypotonia, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773581009",
        "display": "Intellectual disability, craniofacial dysmorphism, cryptorchidism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773583007",
        "display": "Aphonia, deafness, retinal dystrophy, bifid halluces, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773587008",
        "display": "X-linked intellectual disability, cardiomegaly, congestive heart failure syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773621003",
        "display": "Intellectual disability, hypotonia, brachycephaly, pyloric stenosis, cryptorchidism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773643006",
        "display": "Multiple congenital anomalies, hypotonia, seizures syndrome type 2 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773692000",
        "display": "Late-onset localized junctional epidermolysis bullosa, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773735007",
        "display": "Deafness with onychodystrophy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773769008",
        "display": "Ataxia, photosensitivity, short stature syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773772001",
        "display": "Rare non-syndromic intellectual disability (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "773984007",
        "display": "Piebald trait with neurologic defects syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "774068004",
        "display": "AT-hook DNA binding motif containing 1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "774069007",
        "display": "Protein kinase cAMP-dependent type I regulatory subunit beta-related neurodegenerative dementia with intermediate filaments (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "774070008",
        "display": "Fibulin 1-related developmental delay, central nervous system anomaly, syndactyly syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "774102003",
        "display": "Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "774149004",
        "display": "Severe intellectual disability, progressive postnatal microcephaly, midline stereotypic hand movements syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "774203000",
        "display": "Intellectual disability, severe speech delay, mild dysmorphism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "776204008",
        "display": "Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "777998000",
        "display": "Temtamy preaxial brachydactyly syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "778001003",
        "display": "Potassium voltage-gated channel subfamily Q member 2 related epileptic encephalopathy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "778007004",
        "display": "12p12.1 microdeletion syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "778009001",
        "display": "Blepharophimosis, intellectual disability syndrome, Verloes type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "778011005",
        "display": "Severe intellectual disability and progressive spastic paraplegia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "778025006",
        "display": "Atypical hypotonia cystinuria syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "778029000",
        "display": "FAST kinase domains 2-related infantile mitochondrial encephalomyopathy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "778047006",
        "display": "Myoclonic epilepsy in non-progressive encephalopathy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "780827006",
        "display": "Synaptic Ras GTPase activating protein 1- related intellectual disability (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "782723007",
        "display": "Severe intellectual disability, progressive spastic diplegia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "782736007",
        "display": "Intellectual disability, facial dysmorphism syndrome due to SET domain containing 5 haploinsufficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "782753000",
        "display": "Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "782755007",
        "display": "Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "782757004",
        "display": "Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "782772000",
        "display": "Congenital muscular dystrophy with intellectual disability and severe epilepsy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "782825008",
        "display": "Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "782886007",
        "display": "Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "782911008",
        "display": "Hereditary cryohydrocytosis with reduced stomatin (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "782941005",
        "display": "Richieri Costa-da Silva syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "782945001",
        "display": "Ophthalmoplegia, intellectual disability, lingua scrotalis syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "783005002",
        "display": "Severe microbrachycephaly, intellectual disability, athetoid cerebral palsy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "783061008",
        "display": "Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "783089006",
        "display": "Macrocephaly, intellectual disability, autism syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "783161005",
        "display": "Familial dementia British type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "783174004",
        "display": "Congenital muscular dystrophy with intellectual disability (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "783258000",
        "display": "Familial dementia Danish type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "783619003",
        "display": "Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "783702009",
        "display": "X-linked intellectual disability due to glutamate ionotropic receptor AMPA type subunit 3 mutations (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "783703004",
        "display": "White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "785298001",
        "display": "Muscle eye brain disease with bilateral multicystic leukodystrophy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "785726009",
        "display": "Hyperekplexia epilepsy syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "787093004",
        "display": "Developmental delay, facial dysmorphism syndrome due to mediator complex subunit 13 like deficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "787171006",
        "display": "21q22.11q22.12 microdeletion syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "787174003",
        "display": "Intellectual disability, hyperkinetic movement, truncal ataxia syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "787175002",
        "display": "Ankyrin 3 related intellectual disability, sleep disturbance syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "788417006",
        "display": "Alopecia, epilepsy, intellectual disability syndrome Moynahan type (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "788584007",
        "display": "Blepharophimosis, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "788898005",
        "display": "Dementia caused by volatile inhalant (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "788899002",
        "display": "Dementia due to pellagra (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "789170003",
        "display": "Disinhibited behavior due to dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "79341000119107",
        "display": "Mixed dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "79385002",
        "display": "Lowe syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "816067005",
        "display": "Diabetes, hypogonadism, deafness, intellectual disability syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "82351000119105",
        "display": "Altered behavior due to Pick's disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "82361000119107",
        "display": "Altered behavior in dementia due to Huntington chorea (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "82371000119101",
        "display": "Dementia due to multiple sclerosis with altered behavior (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "82381000119103",
        "display": "Epileptic dementia with behavioral disturbance (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "82959004",
        "display": "Dementia paralytica juvenilis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "833326008",
        "display": "Cortical vascular dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "836301008",
        "display": "Amnestic mild cognitive disorder (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "838276009",
        "display": "Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "838441009",
        "display": "Intellectual disability, aphasia, shuffling gait, adducted thumbs syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "840464007",
        "display": "Dementia due to carbon monoxide poisoning (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "840465008",
        "display": "Dementia due to iron deficiency (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "86765009",
        "display": "Mild intellectual disability (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "870260008",
        "display": "Pervasive developmental disorder with marked impairment of functional language with loss of previously acquired skills (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "870261007",
        "display": "Pervasive developmental disorder with marked impairment of functional language without loss of previously acquired skills (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "870262000",
        "display": "Pervasive developmental disorder with disorder of intellectual development without loss of previously acquired skills (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "870263005",
        "display": "Pervasive developmental disorder with impairment of functional language (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "870264004",
        "display": "Pervasive developmental disorder with disorder of intellectual development and pervasive impairment of functional language without loss of previously acquired skills (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "870265003",
        "display": "Pervasive developmental disorder with disorder of intellectual development with loss of previously acquired skills (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "870266002",
        "display": "Pervasive developmental disorder with disorder of intellectual development and marked impairment of functional language with loss of previously acquired skills (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "870267006",
        "display": "Pervasive developmental disorder with disorder of intellectual development and marked impairment of functional language without loss of previously acquired skills (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "870268001",
        "display": "Pervasive developmental disorder with disorder of intellectual development and complete impairment of functional language without loss of previously acquired skills (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "870269009",
        "display": "Pervasive developmental disorder with disorder of intellectual development and absence of functional language with loss of previously acquired skills (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "870270005",
        "display": "Pervasive developmental disorder with disorder of intellectual development and complete impairment of functional language with loss of previously acquired skills (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "870280009",
        "display": "Pervasive developmental disorder with severe impairment of functional language with loss of previously acquired skills (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "870282001",
        "display": "Pervasive developmental disorder with severe impairment of functional language without loss of previously acquired skills (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "870303005",
        "display": "Pervasive developmental disorder with complete impairment of functional language with loss of previously acquired skills (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "870304004",
        "display": "Pervasive developmental disorder with complete impairment of functional language without loss of previously acquired skills (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "870305003",
        "display": "Pervasive developmental disorder with cognitive developmental delay and marked impairment of functional language (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "870306002",
        "display": "Pervasive developmental disorder with complete impairment of functional language (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "870307006",
        "display": "Pervasive developmental disorder with abscence of functional language (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "870308001",
        "display": "Pervasive developmental disorder with cognitive developmental delay and complete impairment of functional language (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "879939002",
        "display": "14q32 deletion syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "88822006",
        "display": "Anterograde amnesia (finding)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "890118006",
        "display": "Mowat-Wilson syndrome due to monosomy 2q22 (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "89392001",
        "display": "Prader-Willi syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "90099008",
        "display": "Subcortical leukoencephalopathy (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "9345005",
        "display": "Dialysis dementia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "9527009",
        "display": "Tetrasomy 12p syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "97751000119108",
        "display": "Altered behavior in Alzheimer's disease (disorder)"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "G31.8",
        "display": "Other specified degenerative diseases of nervous system"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "G31.80",
        "display": "Leukodystrophy, unspecified"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "G31.83",
        "display": "Neurocognitive disorder with Lewy bodies"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "G31.84",
        "display": "Mild cognitive impairment of uncertain or unknown etiology"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "G31.85",
        "display": "Corticobasal degeneration"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "G31.86",
        "display": "Alexander disease"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "G31.89",
        "display": "Other specified degenerative diseases of nervous system"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.3",
        "display": "Sequelae of cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.30",
        "display": "Unspecified sequelae of cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.31",
        "display": "Cognitive deficits following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.310",
        "display": "Attention and concentration deficit following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.311",
        "display": "Memory deficit following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.312",
        "display": "Visuospatial deficit and spatial neglect following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.313",
        "display": "Psychomotor deficit following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.314",
        "display": "Frontal lobe and executive function deficit following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.315",
        "display": "Cognitive social or emotional deficit following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.318",
        "display": "Other symptoms and signs involving cognitive functions following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.319",
        "display": "Unspecified symptoms and signs involving cognitive functions following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.32",
        "display": "Speech and language deficits following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.320",
        "display": "Aphasia following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.321",
        "display": "Dysphasia following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.322",
        "display": "Dysarthria following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.323",
        "display": "Fluency disorder following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.328",
        "display": "Other speech and language deficits following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.33",
        "display": "Monoplegia of upper limb following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.331",
        "display": "Monoplegia of upper limb following cerebral infarction affecting right dominant side"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.332",
        "display": "Monoplegia of upper limb following cerebral infarction affecting left dominant side"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.333",
        "display": "Monoplegia of upper limb following cerebral infarction affecting right non-dominant side"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.334",
        "display": "Monoplegia of upper limb following cerebral infarction affecting left non-dominant side"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.339",
        "display": "Monoplegia of upper limb following cerebral infarction affecting unspecified side"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.34",
        "display": "Monoplegia of lower limb following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.341",
        "display": "Monoplegia of lower limb following cerebral infarction affecting right dominant side"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.342",
        "display": "Monoplegia of lower limb following cerebral infarction affecting left dominant side"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.343",
        "display": "Monoplegia of lower limb following cerebral infarction affecting right non-dominant side"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.344",
        "display": "Monoplegia of lower limb following cerebral infarction affecting left non-dominant side"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.349",
        "display": "Monoplegia of lower limb following cerebral infarction affecting unspecified side"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.35",
        "display": "Hemiplegia and hemiparesis following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.351",
        "display": "Hemiplegia and hemiparesis following cerebral infarction affecting right dominant side"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.352",
        "display": "Hemiplegia and hemiparesis following cerebral infarction affecting left dominant side"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.353",
        "display": "Hemiplegia and hemiparesis following cerebral infarction affecting right non-dominant side"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.354",
        "display": "Hemiplegia and hemiparesis following cerebral infarction affecting left non-dominant side"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.359",
        "display": "Hemiplegia and hemiparesis following cerebral infarction affecting unspecified side"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.36",
        "display": "Other paralytic syndrome following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.361",
        "display": "Other paralytic syndrome following cerebral infarction affecting right dominant side"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.362",
        "display": "Other paralytic syndrome following cerebral infarction affecting left dominant side"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.363",
        "display": "Other paralytic syndrome following cerebral infarction affecting right non-dominant side"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.364",
        "display": "Other paralytic syndrome following cerebral infarction affecting left non-dominant side"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.365",
        "display": "Other paralytic syndrome following cerebral infarction, bilateral"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.369",
        "display": "Other paralytic syndrome following cerebral infarction affecting unspecified side"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.39",
        "display": "Other sequelae of cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.390",
        "display": "Apraxia following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.391",
        "display": "Dysphagia following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.392",
        "display": "Facial weakness following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.393",
        "display": "Ataxia following cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "I69.398",
        "display": "Other sequelae of cerebral infarction"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "R41.8",
        "display": "Other symptoms and signs involving cognitive functions and awareness"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "R41.81",
        "display": "Age-related cognitive decline"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "R41.82",
        "display": "Altered mental status, unspecified"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "R41.83",
        "display": "Borderline intellectual functioning"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "R41.84",
        "display": "Other specified cognitive deficit"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "R41.840",
        "display": "Attention and concentration deficit"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "R41.841",
        "display": "Cognitive communication deficit"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "R41.842",
        "display": "Visuospatial deficit"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "R41.843",
        "display": "Psychomotor deficit"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "R41.844",
        "display": "Frontal lobe and executive function deficit"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "R41.85",
        "display": "Anosognosia"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "R41.89",
        "display": "Other symptoms and signs involving cognitive functions and awareness"
      },
      {
        "system": "http://hl7.org/fhir/sid/icd-10-cm",
        "version": "2025",
        "code": "R41.9",
        "display": "Unspecified symptoms and signs involving cognitive functions and awareness"
      }
    ]
  }
}