ValueSet-2.16.840.1.113762.1.4.1078.177

Sourceus.nlm.vsac#0.11.0:null (v4.0.1)
resourceTypeValueSet
id2.16.840.1.113762.1.4.1078.177
canonicalhttp://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1078.177
version20230601
statusactive
publisherOptum Steward
nameVirtualRealityContraindicationsCognitiveImpairment
titleVirtual reality contraindications cognitive impairment
date2023-06-01T01:01:19-04:00
Usages

This value set contains 754 concepts

Code System Display
   10007009 http://snomed.info/sct Coffin-Siris syndrome (disorder)
   1010630006 http://snomed.info/sct X-linked complicated corpus callosum dysgenesis (disorder)
   101421000119107 http://snomed.info/sct Dementia due to Parkinson's disease (disorder)
   102891000 http://snomed.info/sct Age-related cognitive decline (finding)
   10349009 http://snomed.info/sct Multi-infarct dementia with delirium (disorder)
   10532003 http://snomed.info/sct Primary degenerative dementia of the Alzheimer type, presenile onset, with depression (disorder)
   105421000119105 http://snomed.info/sct Early onset Alzheimer's disease with behavioral disturbance (disorder)
   106021000119105 http://snomed.info/sct Multi-infarct dementia due to atherosclerosis (disorder)
   109478007 http://snomed.info/sct Kohlschutter's syndrome (disorder)
   110355003 http://snomed.info/sct Lack of thinking ability (finding)
   110359009 http://snomed.info/sct Intellectual disability (disorder)
   111480006 http://snomed.info/sct Psychoactive substance-induced organic dementia (disorder)
   1144748009 http://snomed.info/sct Impaired concentration (finding)
   1148924004 http://snomed.info/sct Dementia due to deficiency of folic acid (disorder)
   1156584007 http://snomed.info/sct X-linked intellectual disability hypotonic face syndrome (disorder)
   1156789004 http://snomed.info/sct Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein (disorder)
   1156798001 http://snomed.info/sct Autosomal dominant Alzheimer disease due to mutation of presenilin 2 (disorder)
   1156800008 http://snomed.info/sct Autosomal dominant Alzheimer disease due to mutation of presenilin 1 (disorder)
   1162462009 http://snomed.info/sct Angelman syndrome due to maternal monosomy 15q11q13 (disorder)
   116340000 http://snomed.info/sct Disturbance of cognitive learning (finding)
   1167371007 http://snomed.info/sct Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome (disorder)
   1167375003 http://snomed.info/sct Microcephaly, corpus callosum and cerebellar vermis hypoplasia, facial dysmorphism, intellectual disability syndrome (disorder)
   1169355000 http://snomed.info/sct Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome (disorder)
   1169359006 http://snomed.info/sct Tall stature, intellectual disability, renal anomalies syndrome (disorder)
   1172594000 http://snomed.info/sct Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome (disorder)
   1172624000 http://snomed.info/sct Arginine-glutamic acid dipeptide repeats-related neurodevelopmental syndrome (disorder)
   1172626003 http://snomed.info/sct Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder (disorder)
   1172627007 http://snomed.info/sct Early-onset epilepsy, intellectual disability, brain anomalies syndrome (disorder)
   1172629005 http://snomed.info/sct Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome (disorder)
   1172630000 http://snomed.info/sct Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome (disorder)
   1172685001 http://snomed.info/sct Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome (disorder)
   1172691004 http://snomed.info/sct Chloride voltage-gated channel 4-related X-linked intellectual disability syndrome (disorder)
   1172697000 http://snomed.info/sct X-linked female restricted facial dysmorphism, short stature, choanal atresia, intellectual disability (disorder)
   1172698005 http://snomed.info/sct Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome (disorder)
   1172889005 http://snomed.info/sct Palatal anomalies, widely spaced teeth, facial dysmorphism, developmental delay syndrome (disorder)
   1172899000 http://snomed.info/sct Peripheral myelin protein 22-retinoic acid induced 1 contiguous gene duplication syndrome (disorder)
   1173036000 http://snomed.info/sct Combined oxidative phosphorylation defect type 23 (disorder)
   1173998003 http://snomed.info/sct Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome (disorder)
   1177167002 http://snomed.info/sct Intellectual disability, seizures, abnormal gait, facial dysmorphism syndrome (disorder)
   1177169004 http://snomed.info/sct Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder)
   1177175008 http://snomed.info/sct Skeletal dysplasia, T-cell immunodeficiency, developmental delay syndrome (disorder)
   1179282009 http://snomed.info/sct Severe neurodevelopmental disorder with feeding difficulties, stereotypic hand movement, bilateral cataract (disorder)
   1179283004 http://snomed.info/sct Metopic ridging, ptosis, facial dysmorphism syndrome (disorder)
   1179301003 http://snomed.info/sct Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome (disorder)
   1179408008 http://snomed.info/sct Chromodomain helicase dna-binding protein 3- related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome (disorder)
   1186711002 http://snomed.info/sct G protein subunit beta 5-related intellectual disability, cardiac arrhythmia syndrome (disorder)
   1186713004 http://snomed.info/sct Growth delay, intellectual disability, hepatopathy syndrome (disorder)
   1186721005 http://snomed.info/sct Infantile inflammatory bowel disease with neurological involvement (disorder)
   1186724002 http://snomed.info/sct HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)
   1186729007 http://snomed.info/sct Intellectual disability, cardiac anomalies, short stature, joint laxity syndrome (disorder)
   1186730002 http://snomed.info/sct Gabriele-de Vries syndrome (disorder)
   1186734006 http://snomed.info/sct Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction (disorder)
   1186839009 http://snomed.info/sct Cognitive impairment due to lead toxicity (disorder)
   1186877003 http://snomed.info/sct Dementia due to vitamin E deficiency (disorder)
   1186879000 http://snomed.info/sct Dementia due to thiamine deficiency (disorder)
   1186880002 http://snomed.info/sct Dementia due to cobalamin deficiency (disorder)
   1186881003 http://snomed.info/sct Dementia due to niacin deficiency (disorder)
   1186883000 http://snomed.info/sct Dementia due to nutritional deficiency disorder (disorder)
   1186887004 http://snomed.info/sct Dementia caused by manganese and/or manganese compound (disorder)
   1187004001 http://snomed.info/sct Chronic traumatic encephalopathy (disorder)
   1187038009 http://snomed.info/sct Non-specific syndromic intellectual disability (disorder)
   1187041000 http://snomed.info/sct Stromal antigen 1-related intellectual disability, facial dysmorphism, gastroesophageal reflux syndrome (disorder)
   1187042007 http://snomed.info/sct Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome (disorder)
   1187114007 http://snomed.info/sct Micrognathia, recurrent infections, behavioral abnormalities, mild intellectual disability syndrome (disorder)
   1187122000 http://snomed.info/sct Witteveen Kolk syndrome (disorder)
   1187126002 http://snomed.info/sct Integral membrane protein 2B related amyloidosis (disorder)
   1187195007 http://snomed.info/sct Microcephalic cortical malformations, short stature due to rotatin deficiency (disorder)
   1187210007 http://snomed.info/sct Intellectual disability, epilepsy, extrapyramidal syndrome (disorder)
   1187247007 http://snomed.info/sct WW domain containing adaptor with coiled-coil-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome (disorder)
   1187249005 http://snomed.info/sct VPS11 core subunit of CORVET and HOPS complexes-related autosomal recessive hypomyelinating leukodystrophy (disorder)
   1187250005 http://snomed.info/sct Seizures, scoliosis, macrocephaly syndrome (disorder)
   1187277001 http://snomed.info/sct Short stature, brachydactyly, obesity, global developmental delay syndrome (disorder)
   1187278006 http://snomed.info/sct Spastic paraplegia, severe developmental delay, epilepsy syndrome (disorder)
   1187303004 http://snomed.info/sct Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome (disorder)
   1187304005 http://snomed.info/sct Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome (disorder)
   1187642008 http://snomed.info/sct Macrocephaly, intellectual disability, left ventricular non compaction syndrome (disorder)
   1187644009 http://snomed.info/sct Basel Vanagaite Smirin Yosef syndrome (disorder)
   1197148005 http://snomed.info/sct Sanjad Sakati syndrome (disorder)
   1197588008 http://snomed.info/sct X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome (disorder)
   1197591008 http://snomed.info/sct Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder)
   1197593006 http://snomed.info/sct Intellectual disability, expressive aphasia, facial dysmorphism syndrome (disorder)
   1208341008 http://snomed.info/sct Severe oculo-renal-cerebellar syndrome (disorder)
   1208344000 http://snomed.info/sct Fryns Smeets Thiry syndrome (disorder)
   1208481000 http://snomed.info/sct Progressive cerebello-cerebral atrophy (disorder)
   1208488006 http://snomed.info/sct Special AT-rich sequence-binding protein 2-associated syndrome (disorder)
   1208614008 http://snomed.info/sct Autosomal dominant deafness with onychodystrophy syndrome (disorder)
   1208720000 http://snomed.info/sct Agenesis of corpus callosum, macrocephaly, hypertelorism syndrome (disorder)
   1208727002 http://snomed.info/sct Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome (disorder)
   1208746001 http://snomed.info/sct Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome (disorder)
   1208936008 http://snomed.info/sct Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome (disorder)
   1208987006 http://snomed.info/sct Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome (disorder)
   1217228004 http://snomed.info/sct X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome (disorder)
   1217229007 http://snomed.info/sct Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome (disorder)
   1217371005 http://snomed.info/sct Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome (disorder)
   1217379007 http://snomed.info/sct NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy (disorder)
   1217381009 http://snomed.info/sct Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome (disorder)
   1217382002 http://snomed.info/sct Intellectual disability, autism, speech apraxia, craniofacial dysmorphism syndrome (disorder)
   1220568003 http://snomed.info/sct Glutamine rich 1-related intellectual disability, chondrodysplasia syndrome (disorder)
   1220589007 http://snomed.info/sct Keppen Lubinsky syndrome (disorder)
   1220594007 http://snomed.info/sct Pierpont syndrome (disorder)
   1220597000 http://snomed.info/sct Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome (disorder)
   1220600004 http://snomed.info/sct Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy (disorder)
   1222656005 http://snomed.info/sct Synaptic Ras GTPase activating protein 1-related developmental and epileptic encephalopathy (disorder)
   1222657001 http://snomed.info/sct Prune exopolyphosphatase 1-related neurological syndrome (disorder)
   1222658006 http://snomed.info/sct Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome (disorder)
   1222672002 http://snomed.info/sct 3-methylglutaconic aciduria type 9 (disorder)
   1222706005 http://snomed.info/sct Anterior maxillary protrusion, strabismus, intellectual disability syndrome (disorder)
   1222710008 http://snomed.info/sct Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome (disorder)
   1228886008 http://snomed.info/sct 9q33.3q34.11 microdeletion syndrome (disorder)
   1228890005 http://snomed.info/sct 16p13.2 microdeletion syndrome (disorder)
   1229872004 http://snomed.info/sct Xq25 microduplication syndrome (disorder)
   1229873009 http://snomed.info/sct 17q24.2 microdeletion syndrome (disorder)
   1229875002 http://snomed.info/sct 9q21.13 microdeletion syndrome (disorder)
   1229882003 http://snomed.info/sct 11q22.2q22.3 microdeletion syndrome (disorder)
   1229883008 http://snomed.info/sct 19p13.3 microduplication syndrome (disorder)
   1229891004 http://snomed.info/sct 20q11.2 microdeletion syndrome (disorder)
   1229895008 http://snomed.info/sct 8q24.3 microdeletion syndrome (disorder)
   1230273004 http://snomed.info/sct Megaconial congenital muscular dystrophy (disorder)
   1230376005 http://snomed.info/sct Contactin associated protein 2-related developmental and epileptic encephalopathy (disorder)
   1234774002 http://snomed.info/sct Cognitive impairment caused by ethanol (disorder)
   12348006 http://snomed.info/sct Presenile dementia (disorder)
   1236807002 http://snomed.info/sct Encephalopathy due to mitochondrial and peroxisomal fission defect (disorder)
   1236843008 http://snomed.info/sct Phosphodiesterase 4D haploinsufficiency syndrome (disorder)
   1237179007 http://snomed.info/sct FG syndrome type 1 (disorder)
   1237344003 http://snomed.info/sct Symptomatic form of fragile X syndrome in female carrier (disorder)
   1237418002 http://snomed.info/sct Spastic tetraplegia, thin corpus callosum, progressive postnatal microcephaly syndrome (disorder)
   1237420004 http://snomed.info/sct X-linked intellectual disability, global development delay, facial dysmorphism, sacral caudal remnant syndrome (disorder)
   1237421000 http://snomed.info/sct Pyrroline-5-carboxylate reductase 2 related microcephaly, progressive leukoencephalopathy (disorder)
   1237462006 http://snomed.info/sct nudE neurodevelopment protein 1-related microhydranencephaly (disorder)
   1237512003 http://snomed.info/sct Short stature, developmental delay, congenital heart defect syndrome (disorder)
   1237619001 http://snomed.info/sct Fatty acyl-coenzyme A reductase 1 deficiency (disorder)
   1237623009 http://snomed.info/sct Congenital insensitivity to pain with severe intellectual disability (disorder)
   1237625002 http://snomed.info/sct Autosomal recessive cerebellar ataxia due to CWF19 like cell cycle control factor 1 deficiency (disorder)
   1251452003 http://snomed.info/sct 4q25 proximal deletion syndrome (disorder)
   1251453008 http://snomed.info/sct Lamb Shaffer syndrome (disorder)
   1254650002 http://snomed.info/sct Microcephaly, corpus callosum hypoplasia, intellectual disability, facial dysmorphism syndrome (disorder)
   1254651003 http://snomed.info/sct Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome (disorder)
   1254652005 http://snomed.info/sct Intellectual disability, macrocephaly, hypotonia, behavioral abnormalities syndrome (disorder)
   1254654006 http://snomed.info/sct X-linked intellectual disability, hypotonia, movement disorder syndrome (disorder)
   1255319004 http://snomed.info/sct Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome (disorder)
   1255322002 http://snomed.info/sct Congenital contracture of limbs and face, hypotonia, developmental delay syndrome (disorder)
   1255335006 http://snomed.info/sct X-linked intellectual disability, short stature, overweight syndrome (disorder)
   1258972007 http://snomed.info/sct Baraitser Winter cerebrofrontofacial syndrome (disorder)
   1259121008 http://snomed.info/sct Amyotrophic lateral sclerosis, parkinsonism, dementia complex of West New Guinea (disorder)
   1259123006 http://snomed.info/sct Amyotrophic lateral sclerosis, parkinsonism, dementia complex of Kii Peninsula (disorder)
   1259128002 http://snomed.info/sct Alzheimer disease with psychosis (disorder)
   1260095004 http://snomed.info/sct Menke Hennekam syndrome (disorder)
   1260097007 http://snomed.info/sct Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder)
   1260128008 http://snomed.info/sct Tryptophanyl tRNA synthetase 2, mitochondrial-related combined oxidative phosphorylation defect (disorder)
   1260129000 http://snomed.info/sct Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome (disorder)
   1260130005 http://snomed.info/sct Progressive essential tremor, speech impairment, facial dysmorphism, intellectual disability, abnormal behavior syndrome (disorder)
   1260134001 http://snomed.info/sct Spastic paraplegia, intellectual disability, nystagmus, obesity syndrome (disorder)
   1260143005 http://snomed.info/sct Megalencephaly, severe kyphoscoliosis, overgrowth syndrome (disorder)
   130121000119104 http://snomed.info/sct Dementia due to Rett's syndrome (disorder)
   130964008 http://snomed.info/sct Impaired environmental interpretation syndrome (finding)
   14070001 http://snomed.info/sct Multi-infarct dementia with depression (disorder)
   141601000119107 http://snomed.info/sct Cognitive changes due to organic disorder (finding)
   141991000119109 http://snomed.info/sct Delusions in Alzheimer's disease (disorder)
   142001000119106 http://snomed.info/sct Depressed mood in Alzheimer's disease (disorder)
   142011000119109 http://snomed.info/sct Alzheimer's disease co-occurrent with delirium (disorder)
   142261000119100 http://snomed.info/sct Cognitive deficit in attention (finding)
   15182000 http://snomed.info/sct Coffin-Lowry syndrome (disorder)
   15662003 http://snomed.info/sct Senile dementia (disorder)
   1581000119101 http://snomed.info/sct Dementia of the Alzheimer type with behavioral disturbance (disorder)
   1591000119103 http://snomed.info/sct Dementia with behavioral disturbance (disorder)
   15928141000119107 http://snomed.info/sct Cognitive impairment co-occurrent and due to human immunodeficiency virus infection (disorder)
   16219201000119101 http://snomed.info/sct Behavioral disturbance co-occurrent and due to late onset Alzheimer dementia (disorder)
   162200009 http://snomed.info/sct Temporary loss of memory (finding)
   16276361000119109 http://snomed.info/sct Vascular dementia without behavioral disturbance (disorder)
   16703491000119101 http://snomed.info/sct Memory deficit due to and following spontaneous intracerebral hemorrhage (disorder)
   16703551000119107 http://snomed.info/sct Memory deficit due to and following cerebrovascular disease (disorder)
   16703601000119109 http://snomed.info/sct Memory deficit due to and following spontaneous subarachnoid hemorrhage (disorder)
   16703661000119105 http://snomed.info/sct Memory deficit due to and following cerebrovascular accident (disorder)
   16703711000119100 http://snomed.info/sct Memory deficit due to and following embolic cerebrovascular accident (disorder)
   16703761000119102 http://snomed.info/sct Memory deficit due to and following ischemic cerebrovascular accident (disorder)
   16703821000119101 http://snomed.info/sct Memory deficit due to and following hemorrhagic cerebrovascular accident (disorder)
   17827007 http://snomed.info/sct Cross syndrome (disorder)
   18541000119100 http://snomed.info/sct Borderline cognitive developmental delay (disorder)
   191449005 http://snomed.info/sct Uncomplicated senile dementia (disorder)
   191451009 http://snomed.info/sct Uncomplicated presenile dementia (disorder)
   191452002 http://snomed.info/sct Presenile dementia with delirium (disorder)
   191454001 http://snomed.info/sct Presenile dementia with paranoia (disorder)
   191455000 http://snomed.info/sct Presenile dementia with depression (disorder)
   191457008 http://snomed.info/sct Senile dementia with depressive or paranoid features (disorder)
   191458003 http://snomed.info/sct Senile dementia with paranoia (disorder)
   191459006 http://snomed.info/sct Senile dementia with depression (disorder)
   191461002 http://snomed.info/sct Senile dementia with delirium (disorder)
   191463004 http://snomed.info/sct Uncomplicated arteriosclerotic dementia (disorder)
   191464005 http://snomed.info/sct Arteriosclerotic dementia with delirium (disorder)
   191465006 http://snomed.info/sct Arteriosclerotic dementia with paranoia (disorder)
   191466007 http://snomed.info/sct Arteriosclerotic dementia with depression (disorder)
   191493005 http://snomed.info/sct Dementia caused by drug (disorder)
   191519005 http://snomed.info/sct Dementia associated with another disease (disorder)
   192071009 http://snomed.info/sct Mild memory disturbance (finding)
   205615000 http://snomed.info/sct Trisomy 21- meiotic nondisjunction (disorder)
   205616004 http://snomed.info/sct Trisomy 21- mitotic nondisjunction mosaicism (disorder)
   21634003 http://snomed.info/sct Borjeson-Forssman-Lehmann syndrome (disorder)
   21921000119103 http://snomed.info/sct Dementia co-occurrent and due to Pick's disease (disorder)
   22381000119105 http://snomed.info/sct Primary degenerative dementia (disorder)
   225037001 http://snomed.info/sct Minor memory lapses (finding)
   225038006 http://snomed.info/sct Memory lapses (finding)
   225039003 http://snomed.info/sct Mixes past with present (finding)
   229676007 http://snomed.info/sct Language-related cognitive disorder (disorder)
   230265002 http://snomed.info/sct Familial Alzheimer's disease of early onset (disorder)
   230266001 http://snomed.info/sct Non-familial Alzheimer's disease of early onset (disorder)
   230267005 http://snomed.info/sct Familial Alzheimer's disease of late onset (disorder)
   230268000 http://snomed.info/sct Non-familial Alzheimer's disease of late onset (disorder)
   230269008 http://snomed.info/sct Focal Alzheimer's disease (disorder)
   230280008 http://snomed.info/sct Progressive aphasia in Alzheimer's disease (disorder)
   230282000 http://snomed.info/sct Post-traumatic dementia (disorder)
   230285003 http://snomed.info/sct Vascular dementia of acute onset (disorder)
   230286002 http://snomed.info/sct Subcortical vascular dementia (disorder)
   230287006 http://snomed.info/sct Mixed cortical and subcortical vascular dementia (disorder)
   230289009 http://snomed.info/sct Patchy dementia (disorder)
   230299004 http://snomed.info/sct Juvenile onset Huntington's disease (disorder)
   230300007 http://snomed.info/sct Late onset Huntington's disease (disorder)
   230301006 http://snomed.info/sct Akinetic-rigid form of Huntington's disease (disorder)
   230736007 http://snomed.info/sct Transient global amnesia (finding)
   232059000 http://snomed.info/sct Laurence-Moon syndrome (disorder)
   234146006 http://snomed.info/sct Hennekam lymphangiectasia-lymphedema syndrome (disorder)
   236529001 http://snomed.info/sct Prune belly syndrome with pulmonic stenosis, intellectual disability and deafness (disorder)
   2421000119107 http://snomed.info/sct Hallucinations co-occurrent and due to late onset dementia (disorder)
   247607004 http://snomed.info/sct Amnesia for day to day facts (finding)
   247611005 http://snomed.info/sct Amnesia for important personal information (finding)
   253176002 http://snomed.info/sct Gillespie syndrome (disorder)
   25470001000004105 http://snomed.info/sct Cognitive impairment due to multiple sclerosis (finding)
   25772007 http://snomed.info/sct Multi-infarct dementia with delusions (disorder)
   26581009 http://snomed.info/sct Retrospective falsification (finding)
   26852004 http://snomed.info/sct Primary degenerative dementia of the Alzheimer type, senile onset, with depression (disorder)
   268612007 http://snomed.info/sct Senile and presenile organic psychotic conditions (disorder)
   26929004 http://snomed.info/sct Alzheimer's disease (disorder)
   275277000 http://snomed.info/sct Post-traumatic amnesia (finding)
   278857002 http://snomed.info/sct Dementia of frontal lobe type (disorder)
   281004 http://snomed.info/sct Dementia associated with alcoholism (disorder)
   283878007 http://snomed.info/sct Impairment of registration (finding)
   288631000119104 http://snomed.info/sct Vascular dementia with behavioral disturbance (disorder)
   290621000119101 http://snomed.info/sct Cognitive deficit due to and following cerebrovascular disease (disorder)
   291621000119109 http://snomed.info/sct Cognitive deficit due to and following nontraumatic subarachnoid hemorrhage (disorder)
   291711000119109 http://snomed.info/sct Cognitive deficit due to and following nontraumatic intracerebral hemorrhage (disorder)
   293671000119109 http://snomed.info/sct Behavioral disturbance due to multi-infarct dementia (disorder)
   31081000119101 http://snomed.info/sct Presenile dementia with delusions (disorder)
   31216003 http://snomed.info/sct Profound intellectual disability (disorder)
   312991009 http://snomed.info/sct Senile dementia of the Lewy body type (disorder)
   32541007 http://snomed.info/sct Paramnesia (finding)
   32875003 http://snomed.info/sct Inhalant-induced persisting dementia (disorder)
   33982008 http://snomed.info/sct Hyperphosphatasemia with intellectual disability (disorder)
   371024007 http://snomed.info/sct Senile dementia with delusion (disorder)
   371026009 http://snomed.info/sct Senile dementia with psychosis (disorder)
   371045000 http://snomed.info/sct Translocation Down syndrome (disorder)
   386806002 http://snomed.info/sct Impaired cognition (finding)
   386807006 http://snomed.info/sct Memory impairment (finding)
   395689002 http://snomed.info/sct Transient epileptic amnesia (finding)
   40425004 http://snomed.info/sct Postconcussion syndrome (disorder)
   40700009 http://snomed.info/sct Severe intellectual disability (disorder)
   41040004 http://snomed.info/sct Complete trisomy 21 syndrome (disorder)
   412787009 http://snomed.info/sct Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth (disorder)
   416106008 http://snomed.info/sct Disturbance of memory for order of events (finding)
   416780008 http://snomed.info/sct Primary degenerative dementia of the Alzheimer type, presenile onset (disorder)
   416975007 http://snomed.info/sct Primary degenerative dementia of the Alzheimer type, senile onset (disorder)
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   428051000124108 http://snomed.info/sct Mild dementia (disorder)
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   672561000119103 http://snomed.info/sct Cognitive deficit due to and following ischemic cerebrovascular accident (disorder)
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   726727003 http://snomed.info/sct X-linked intellectual disability Hedera type (disorder)
   726732002 http://snomed.info/sct X-linked intellectual disability Nascimento type (disorder)
   732246009 http://snomed.info/sct X-linked intellectual disability, limb spasticity, retinal dystrophy, diabetes insipidus syndrome (disorder)
   732251003 http://snomed.info/sct Cortical blindness, intellectual disability, polydactyly syndrome (disorder)
   732954002 http://snomed.info/sct Osteopenia, intellectual disability, sparse hair syndrome (disorder)
   732957009 http://snomed.info/sct Brachydactyly and preaxial hallux varus syndrome (disorder)
   732958004 http://snomed.info/sct Spastic paraplegia with precocious puberty syndrome (disorder)
   732961003 http://snomed.info/sct Branchial dysplasia, intellectual disability, inguinal hernia syndrome (disorder)
   733031004 http://snomed.info/sct Epilepsy, microcephaly, skeletal dysplasia syndrome (disorder)
   733032006 http://snomed.info/sct Epilepsy telangiectasia syndrome (disorder)
   733049004 http://snomed.info/sct Encephalopathy, intracerebral calcification, retinal degeneration syndrome (disorder)
   733050004 http://snomed.info/sct Dysmorphism, short stature, deafness, disorder of sex development syndrome (disorder)
   733062000 http://snomed.info/sct Marfanoid habitus with autosomal recessive intellectual disability syndrome (disorder)
   733072002 http://snomed.info/sct Alaninuria, microcephaly, dwarfism, enamel hypoplasia, diabetes mellitus syndrome (disorder)
   733086003 http://snomed.info/sct Pseudoprogeria syndrome (disorder)
   733088002 http://snomed.info/sct Preaxial polydactyly, colobomata, intellectual disability syndrome (disorder)
   733097003 http://snomed.info/sct Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome (disorder)
   733110004 http://snomed.info/sct Van den Bosch syndrome (disorder)
   733116005 http://snomed.info/sct Aniridia, renal agenesis, psychomotor retardation syndrome (disorder)
   733117001 http://snomed.info/sct Thumb stiffness, brachydactyly, intellectual disability syndrome (disorder)
   733184002 http://snomed.info/sct Dementia caused by heavy metal exposure (disorder)
   733185001 http://snomed.info/sct Dementia following injury caused by exposure to ionizing radiation (disorder)
   733190003 http://snomed.info/sct Dementia due to primary malignant neoplasm of brain (disorder)
   733191004 http://snomed.info/sct Dementia due to chronic subdural hematoma (disorder)
   733192006 http://snomed.info/sct Dementia due to herpes encephalitis (disorder)
   733193001 http://snomed.info/sct Dementia co-occurrent and due to progressive multifocal leukoencephalopathy (disorder)
   733194007 http://snomed.info/sct Dementia co-occurrent and due to Down syndrome (disorder)
   733417008 http://snomed.info/sct Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome (disorder)
   733419006 http://snomed.info/sct Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome (disorder)
   733455003 http://snomed.info/sct Spastic paraplegia, glaucoma, intellectual disability syndrome (disorder)
   733472005 http://snomed.info/sct Microcephalus, glomerulonephritis, marfanoid habitus syndrome (disorder)
   733522005 http://snomed.info/sct Megalocornea with intellectual disability syndrome (disorder)
   734017008 http://snomed.info/sct Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder)
   734173003 http://snomed.info/sct Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome (disorder)
   734349003 http://snomed.info/sct Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder)
   736314008 http://snomed.info/sct Dissociative neurological symptom disorder co-occurrent with cognitive symptoms (disorder)
   736317001 http://snomed.info/sct Impaired executive functioning (finding)
   762298000 http://snomed.info/sct Cognitive impairment due to toxicity of substance (finding)
   762350007 http://snomed.info/sct Dementia due to prion disease (disorder)
   762351006 http://snomed.info/sct Dementia due to and following injury of head (disorder)
   762707000 http://snomed.info/sct Subcortical dementia (disorder)
   763136000 http://snomed.info/sct Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome (disorder)
   763186006 http://snomed.info/sct Grubben, De Cock, Borghgraef syndrome (disorder)
   763278004 http://snomed.info/sct Facial dysmorphism, cleft palate, loose skin syndrome (disorder)
   763320005 http://snomed.info/sct Craniofaciofrontodigital syndrome (disorder)
   763344007 http://snomed.info/sct Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome (disorder)
   763350002 http://snomed.info/sct Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome (disorder)
   763353000 http://snomed.info/sct Cerebrofacioarticular syndrome (disorder)
   763404001 http://snomed.info/sct Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome (disorder)
   763615003 http://snomed.info/sct Aortic arch anomaly, facial dysmorphism, intellectual disability syndrome (disorder)
   763618001 http://snomed.info/sct Wiedemann Steiner syndrome (disorder)
   763626009 http://snomed.info/sct Intellectual disability due to nutritional deficiency (disorder)
   763665007 http://snomed.info/sct Craniodigital syndrome and intellectual disability syndrome (disorder)
   763722004 http://snomed.info/sct Hypotonia, speech impairment, severe cognitive delay syndrome (disorder)
   763741001 http://snomed.info/sct Intellectual disability, alacrima, achalasia syndrome (disorder)
   763742008 http://snomed.info/sct Intellectual disability, polydactyly, uncombable hair syndrome (disorder)
   763743003 http://snomed.info/sct Intellectual disability, spasticity, ectrodactyly syndrome (disorder)
   763744009 http://snomed.info/sct Intellectual disability, brachydactyly, Pierre Robin syndrome (disorder)
   763745005 http://snomed.info/sct Intellectual disability Wolff type (disorder)
   763773007 http://snomed.info/sct Macrocephaly and developmental delay syndrome (disorder)
   763795006 http://snomed.info/sct Malan overgrowth syndrome (disorder)
   763797003 http://snomed.info/sct Agenesis of corpus callosum and abnormal genitalia syndrome (disorder)
   763837007 http://snomed.info/sct Oro-facial digital syndrome type 14 (disorder)
   763861000 http://snomed.info/sct Pachygyria, intellectual disability, epilepsy syndrome (disorder)
   764455002 http://snomed.info/sct Cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, skeletal dysplasia syndrome (disorder)
   764732004 http://snomed.info/sct Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome (disorder)
   764861005 http://snomed.info/sct Intellectual disability Birk-Barel type (disorder)
   764950001 http://snomed.info/sct Cryptorchidism, arachnodactyly, intellectual disability syndrome (disorder)
   764959000 http://snomed.info/sct Intellectual disability, myopathy, short stature, endocrine defect syndrome (disorder)
   765089003 http://snomed.info/sct Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome (disorder)
   765170001 http://snomed.info/sct Sodium voltage-gated channel alpha subunit 8-related epilepsy with encephalopathy (disorder)
   765325002 http://snomed.info/sct Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease (disorder)
   765434008 http://snomed.info/sct Human immunodeficiency virus type I enhancer binding protein 2 related intellectual disability (disorder)
   765471005 http://snomed.info/sct X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome (disorder)
   765758008 http://snomed.info/sct Microcephalic primordial dwarfism Montreal type (disorder)
   765761009 http://snomed.info/sct Brachydactyly, mesomelia, intellectual disability, heart defect syndrome (disorder)
   766753005 http://snomed.info/sct Nijmegen breakage syndrome-like disorder (disorder)
   766824003 http://snomed.info/sct Activity dependent neuroprotector homeobox related multiple congenital anomalies, intellectual disability, autism spectrum disorder (disorder)
   766870005 http://snomed.info/sct Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder)
   766871009 http://snomed.info/sct Diencephalic mesencephalic junction dysplasia (disorder)
   76789006 http://snomed.info/sct Information conversion problem (finding)
   768473009 http://snomed.info/sct Purine rich element binding protein A syndrome (disorder)
   768677000 http://snomed.info/sct Protein phosphatase 2 regulatory subunit b (b56) delta-related intellectual disability (disorder)
   76880004 http://snomed.info/sct Angelman syndrome (disorder)
   768843007 http://snomed.info/sct Tall stature, intellectual disability, facial dysmorphism syndrome (disorder)
   770404004 http://snomed.info/sct Autosomal recessive chorioretinopathy and microcephaly syndrome (disorder)
   770431001 http://snomed.info/sct Early-onset epileptic encephalopathy and intellectual disability due to glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A mutation (disorder)
   770564004 http://snomed.info/sct Microcephalic primordial dwarfism Alazami type (disorder)
   770565003 http://snomed.info/sct Microcephalic primordial dwarfism Dauber type (disorder)
   770604006 http://snomed.info/sct X-linked cerebral, cerebellar, coloboma syndrome (disorder)
   770679002 http://snomed.info/sct Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome (disorder)
   770719004 http://snomed.info/sct 3q27.3 microdeletion syndrome (disorder)
   770721009 http://snomed.info/sct Microcephaly, thin corpus callosum, intellectual disability syndrome (disorder)
   770723007 http://snomed.info/sct Optic atrophy, intellectual disability syndrome (disorder)
   770725000 http://snomed.info/sct Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly (disorder)
   770750002 http://snomed.info/sct Intellectual disability, seizures, macrocephaly, obesity syndrome (disorder)
   770751003 http://snomed.info/sct Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome (disorder)
   770755007 http://snomed.info/sct Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome (disorder)
   770756008 http://snomed.info/sct 2p13.2 microdeletion syndrome (disorder)
   770790004 http://snomed.info/sct Developmental delay with autism spectrum disorder and gait instability (disorder)
   770793002 http://snomed.info/sct 5p13 microduplication syndrome (disorder)
   770794008 http://snomed.info/sct 11p15.4 microduplication syndrome (disorder)
   770898002 http://snomed.info/sct Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency (disorder)
   770901001 http://snomed.info/sct Autosomal recessive intellectual disability, motor dysfunction, multiple joint contracture syndrome (disorder)
   770907002 http://snomed.info/sct Kagami Ogata syndrome (disorder)
   770941005 http://snomed.info/sct Alopecia, progressive neurological defect, endocrinopathy syndrome (disorder)
   771074000 http://snomed.info/sct Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome (disorder)
   771077007 http://snomed.info/sct Intellectual disability, short stature, hypertelorism syndrome (disorder)
   771148008 http://snomed.info/sct X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome (disorder)
   771149000 http://snomed.info/sct Hepatic fibrosis, renal cyst, intellectual disability syndrome (disorder)
   771179007 http://snomed.info/sct Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome (disorder)
   771262009 http://snomed.info/sct Pseudoleprechaunism syndrome Patterson type (disorder)
   771336003 http://snomed.info/sct Polymicrogyria with optic nerve hypoplasia (disorder)
   771417007 http://snomed.info/sct Cognitive dysfunction following surgical procedure (disorder)
   771448004 http://snomed.info/sct Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency (disorder)
   771470001 http://snomed.info/sct Jawad syndrome (disorder)
   771472009 http://snomed.info/sct Developmental and speech delay due to SRY-box 5 deficiency (disorder)
   771476007 http://snomed.info/sct Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome (disorder)
   771477003 http://snomed.info/sct 15q overgrowth syndrome (disorder)
   771512003 http://snomed.info/sct Autism spectrum disorder due to AUTS2 activator of transcription and developmental regulator deficiency (disorder)
   772127009 http://snomed.info/sct White Sutton syndrome (disorder)
   772224009 http://snomed.info/sct Warburg micro syndrome (disorder)
   772225005 http://snomed.info/sct RAB18, member RAS oncogene family deficiency (disorder)
   77287004 http://snomed.info/sct Borderline intellectual disability (disorder)
   773230003 http://snomed.info/sct Cyclin-dependent kinase-like 5 deficiency (disorder)
   773274001 http://snomed.info/sct X-linked intellectual disability, craniofacioskeletal syndrome (disorder)
   773303005 http://snomed.info/sct Spondyloepimetaphyseal dysplasia Genevieve type (disorder)
   773307006 http://snomed.info/sct Zechi Ceide syndrome (disorder)
   773329005 http://snomed.info/sct CK syndrome (disorder)
   773400009 http://snomed.info/sct Severe feeding difficulties, failure to thrive, microcephaly due to ASXL transcriptional regulator 3 deficiency syndrome (disorder)
   773404000 http://snomed.info/sct Roifman syndrome (disorder)
   773405004 http://snomed.info/sct Intellectual disability with strabismus syndrome (disorder)
   773416006 http://snomed.info/sct Intellectual disability, facial dysmorphism, hand anomalies syndrome (disorder)
   773418007 http://snomed.info/sct Xylosyltransferase 1 congenital disorder of glycosylation (disorder)
   773419004 http://snomed.info/sct Severe intellectual disability, short stature, behavioral abnormalities, facial dysmorphism syndrome (disorder)
   773493002 http://snomed.info/sct 9q31.1q31.3 microdeletion syndrome (disorder)
   773494008 http://snomed.info/sct 14q24.1q24.3 microdeletion syndrome (disorder)
   773498006 http://snomed.info/sct Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency (disorder)
   773547003 http://snomed.info/sct 13q12.3 microdeletion syndrome (disorder)
   773548008 http://snomed.info/sct Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome (disorder)
   773551001 http://snomed.info/sct Severe intellectual disability, poor language, strabismus, grimacing face, long fingers syndrome (disorder)
   773552008 http://snomed.info/sct Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome (disorder)
   773553003 http://snomed.info/sct Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome (disorder)
   773554009 http://snomed.info/sct THO complex 6-related developmental delay, microcephaly, facial dysmorphism syndrome (disorder)
   773556006 http://snomed.info/sct Short ulna, dysmorphism, hypotonia, intellectual disability syndrome (disorder)
   773581009 http://snomed.info/sct Intellectual disability, craniofacial dysmorphism, cryptorchidism syndrome (disorder)
   773583007 http://snomed.info/sct Aphonia, deafness, retinal dystrophy, bifid halluces, intellectual disability syndrome (disorder)
   773587008 http://snomed.info/sct X-linked intellectual disability, cardiomegaly, congestive heart failure syndrome (disorder)
   773621003 http://snomed.info/sct Intellectual disability, hypotonia, brachycephaly, pyloric stenosis, cryptorchidism syndrome (disorder)
   773670004 http://snomed.info/sct Distal Xq28 microduplication syndrome (disorder)
   773692000 http://snomed.info/sct Late-onset localized junctional epidermolysis bullosa, intellectual disability syndrome (disorder)
   773735007 http://snomed.info/sct Deafness with onychodystrophy syndrome (disorder)
   773769008 http://snomed.info/sct Ataxia, photosensitivity, short stature syndrome (disorder)
   773772001 http://snomed.info/sct Rare non-syndromic intellectual disability (disorder)
   773984007 http://snomed.info/sct Piebald trait with neurologic defects syndrome (disorder)
   774068004 http://snomed.info/sct AT-hook DNA binding motif containing 1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome (disorder)
   774069007 http://snomed.info/sct Protein kinase cAMP-dependent type I regulatory subunit beta-related neurodegenerative dementia with intermediate filaments (disorder)
   774070008 http://snomed.info/sct Fibulin 1-related developmental delay, central nervous system anomaly, syndactyly syndrome (disorder)
   774102003 http://snomed.info/sct Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome (disorder)
   774149004 http://snomed.info/sct Severe intellectual disability, progressive postnatal microcephaly, midline stereotypic hand movements syndrome (disorder)
   774203000 http://snomed.info/sct Intellectual disability, severe speech delay, mild dysmorphism syndrome (disorder)
   776204008 http://snomed.info/sct Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome (disorder)
   777998000 http://snomed.info/sct Temtamy preaxial brachydactyly syndrome (disorder)
   778007004 http://snomed.info/sct 12p12.1 microdeletion syndrome (disorder)
   778009001 http://snomed.info/sct Blepharophimosis, intellectual disability syndrome, Verloes type (disorder)
   778011005 http://snomed.info/sct Severe intellectual disability and progressive spastic paraplegia (disorder)
   778025006 http://snomed.info/sct Atypical hypotonia cystinuria syndrome (disorder)
   780827006 http://snomed.info/sct Synaptic Ras GTPase activating protein 1- related intellectual disability (disorder)
   782723007 http://snomed.info/sct Severe intellectual disability, progressive spastic diplegia syndrome (disorder)
   782736007 http://snomed.info/sct Intellectual disability, facial dysmorphism syndrome due to SET domain containing 5 haploinsufficiency (disorder)
   782753000 http://snomed.info/sct Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome (disorder)
   782755007 http://snomed.info/sct Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome (disorder)
   782757004 http://snomed.info/sct Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome (disorder)
   782772000 http://snomed.info/sct Congenital muscular dystrophy with intellectual disability and severe epilepsy (disorder)
   782886007 http://snomed.info/sct Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome (disorder)
   782911008 http://snomed.info/sct Hereditary cryohydrocytosis with reduced stomatin (disorder)
   782941005 http://snomed.info/sct Richieri Costa-da Silva syndrome (disorder)
   782945001 http://snomed.info/sct Ophthalmoplegia, intellectual disability, lingua scrotalis syndrome (disorder)
   783005002 http://snomed.info/sct Severe microbrachycephaly, intellectual disability, athetoid cerebral palsy syndrome (disorder)
   783061008 http://snomed.info/sct Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion (disorder)
   783089006 http://snomed.info/sct Macrocephaly, intellectual disability, autism syndrome (disorder)
   783161005 http://snomed.info/sct Familial dementia British type (disorder)
   783174004 http://snomed.info/sct Congenital muscular dystrophy with intellectual disability (disorder)
   783258000 http://snomed.info/sct Familial dementia Danish type (disorder)
   783619003 http://snomed.info/sct Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion (disorder)
   783702009 http://snomed.info/sct X-linked intellectual disability due to glutamate ionotropic receptor AMPA type subunit 3 mutations (disorder)
   783703004 http://snomed.info/sct White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome (disorder)
   785298001 http://snomed.info/sct Muscle eye brain disease with bilateral multicystic leukodystrophy (disorder)
   785726009 http://snomed.info/sct Hyperekplexia epilepsy syndrome (disorder)
   787093004 http://snomed.info/sct Developmental delay, facial dysmorphism syndrome due to mediator complex subunit 13 like deficiency (disorder)
   787171006 http://snomed.info/sct 21q22.11q22.12 microdeletion syndrome (disorder)
   787174003 http://snomed.info/sct Intellectual disability, hyperkinetic movement, truncal ataxia syndrome (disorder)
   787175002 http://snomed.info/sct Ankyrin 3 related intellectual disability, sleep disturbance syndrome (disorder)
   788417006 http://snomed.info/sct Alopecia, epilepsy, intellectual disability syndrome Moynahan type (disorder)
   788584007 http://snomed.info/sct Blepharophimosis, intellectual disability syndrome (disorder)
   788898005 http://snomed.info/sct Dementia caused by volatile inhalant (disorder)
   788899002 http://snomed.info/sct Dementia due to pellagra (disorder)
   789170003 http://snomed.info/sct Disinhibited behavior due to dementia (disorder)
   79341000119107 http://snomed.info/sct Mixed dementia (disorder)
   79385002 http://snomed.info/sct Lowe syndrome (disorder)
   816067005 http://snomed.info/sct Diabetes, hypogonadism, deafness, intellectual disability syndrome (disorder)
   82361000119107 http://snomed.info/sct Altered behavior in dementia due to Huntington chorea (disorder)
   82371000119101 http://snomed.info/sct Dementia due to multiple sclerosis with altered behavior (disorder)
   82381000119103 http://snomed.info/sct Epileptic dementia with behavioral disturbance (disorder)
   82959004 http://snomed.info/sct Dementia paralytica juvenilis (disorder)
   833326008 http://snomed.info/sct Cortical vascular dementia (disorder)
   838276009 http://snomed.info/sct Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder)
   838441009 http://snomed.info/sct Intellectual disability, aphasia, shuffling gait, adducted thumbs syndrome (disorder)
   840464007 http://snomed.info/sct Dementia due to carbon monoxide poisoning (disorder)
   840465008 http://snomed.info/sct Dementia due to iron deficiency (disorder)
   840505007 http://snomed.info/sct Down syndrome co-occurrent with leukemoid reaction associated transient neonatal pustulosis (disorder)
   86765009 http://snomed.info/sct Mild intellectual disability (disorder)
   870262000 http://snomed.info/sct Pervasive developmental disorder with disorder of intellectual development without loss of previously acquired skills (disorder)
   870264004 http://snomed.info/sct Pervasive developmental disorder with disorder of intellectual development and pervasive impairment of functional language without loss of previously acquired skills (disorder)
   870265003 http://snomed.info/sct Pervasive developmental disorder with disorder of intellectual development with loss of previously acquired skills (disorder)
   870266002 http://snomed.info/sct Pervasive developmental disorder with disorder of intellectual development and marked impairment of functional language with loss of previously acquired skills (disorder)
   870267006 http://snomed.info/sct Pervasive developmental disorder with disorder of intellectual development and marked impairment of functional language without loss of previously acquired skills (disorder)
   870268001 http://snomed.info/sct Pervasive developmental disorder with disorder of intellectual development and complete impairment of functional language without loss of previously acquired skills (disorder)
   870269009 http://snomed.info/sct Pervasive developmental disorder with disorder of intellectual development and absence of functional language with loss of previously acquired skills (disorder)
   870270005 http://snomed.info/sct Pervasive developmental disorder with disorder of intellectual development and complete impairment of functional language with loss of previously acquired skills (disorder)
   870305003 http://snomed.info/sct Pervasive developmental disorder with cognitive developmental delay and marked impairment of functional language (disorder)
   870308001 http://snomed.info/sct Pervasive developmental disorder with cognitive developmental delay and complete impairment of functional language (disorder)
   879939002 http://snomed.info/sct 14q32 deletion syndrome (disorder)
   88822006 http://snomed.info/sct Anterograde amnesia (finding)
   890118006 http://snomed.info/sct Mowat-Wilson syndrome due to monosomy 2q22 (disorder)
   90099008 http://snomed.info/sct Subcortical leukoencephalopathy (disorder)
   9345005 http://snomed.info/sct Dialysis dementia (disorder)
   9527009 http://snomed.info/sct Tetrasomy 12p syndrome (disorder)
   97751000119108 http://snomed.info/sct Altered behavior in Alzheimer's disease (disorder)

Produced 08 Sep 2023