| Package | us.nlm.vsac |
| Type | ValueSet |
| Id | Id |
| FHIR Version | R4 |
| Source | http://fhir.org/packages/us.nlm.vsac/https://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1247.137/expansion |
| Url | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1247.137 |
| Version | 20240626 |
| Status | active |
| Date | 2024-06-26T01:12:04-04:00 |
| Name | CognitiveDisorderDiagnosis |
| Title | Cognitive disorder Diagnosis |
| Experimental | False |
| Realm | us |
| Authority | hl7 |
| 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) |
No resources found
| CodeSystem | |
http://snomed.info/sct  | SNOMED CT (all versions) |
| http://hl7.org/fhir/sid/icd-10-cm | International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM) |
| http://snomed.info/sct | SNOMED codes used in this IG |
| http://snomed.info/sct | veri |
| http://hl7.org/fhir/sid/icd-10-cm | International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM) |
| http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1222.1525 | Cognitive disorder Diagnosis ICD10 |
| http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1222.1526 | Cognitive disorder SCT |
FHIR{
"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:4e695c2c-dda1-44ed-9709-c65c26b4ad56",
"timestamp" : "2025-05-11T07:00:41-04:00",
"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" : & "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)"
},
&nbs on/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"
}
]
},
"text" : {
}
}
XIG built as of ??metadata-date??. Found ??metadata-resources?? resources in ??metadata-packages?? packages.