Source | us.nlm.vsac#0.11.0:null (v4.0.1) |
resourceType | ValueSet |
id | 2.16.840.1.113883.3.464.1003.1187 |
canonical | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.1187 |
version | 20220913 |
status | active |
publisher | NCQA PHEMUR |
name | CognitiveImpairment |
title | Cognitive Impairment |
date | 2022-09-13T01:02:16-04:00 |
experimental | false |
Usages |
|
This value set contains 435 concepts
Code | System | Display |
101421000119107 | http://snomed.info/sct | Dementia due to Parkinson's disease (disorder) |
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) |
110359009 | http://snomed.info/sct | Intellectual disability (disorder) |
111480006 | http://snomed.info/sct | Psychoactive substance-induced organic dementia (disorder) |
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) |
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) |
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) |
1172628002 | http://snomed.info/sct | TBC1 domain containing kinase-related intellectual disability 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) |
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) |
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) |
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) |
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) |
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) |
1187114007 | http://snomed.info/sct | Micrognathia, recurrent infections, behavioral abnormalities, mild intellectual disability syndrome (disorder) |
1187126002 | http://snomed.info/sct | Integral membrane protein 2B related amyloidosis (disorder) |
1187210007 | http://snomed.info/sct | Intellectual disability, epilepsy, extrapyramidal 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) |
12348006 | http://snomed.info/sct | Presenile dementia (disorder) |
130121000119104 | http://snomed.info/sct | Dementia due to Rett's syndrome (disorder) |
14070001 | http://snomed.info/sct | Multi-infarct dementia with depression (disorder) |
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) |
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) |
16219201000119101 | http://snomed.info/sct | Behavioral disturbance co-occurrent and due to late onset Alzheimer dementia (disorder) |
16276361000119109 | http://snomed.info/sct | Vascular dementia without behavioral disturbance (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) |
191689008 | http://snomed.info/sct | Active infantile autism (disorder) |
191690004 | http://snomed.info/sct | Residual infantile autism (disorder) |
191692007 | http://snomed.info/sct | Active disintegrative psychoses (disorder) |
191693002 | http://snomed.info/sct | Residual disintegrative psychoses (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) |
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) |
230270009 | http://snomed.info/sct | Frontotemporal dementia (disorder) |
230271008 | http://snomed.info/sct | Pick's disease with Pick bodies (disorder) |
230272001 | http://snomed.info/sct | Pick's disease with Pick cells and no Pick bodies (disorder) |
230274000 | http://snomed.info/sct | Frontal lobe degeneration with motor neurone disease (disorder) |
230280008 | http://snomed.info/sct | Progressive aphasia in Alzheimer's disease (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) |
230288001 | http://snomed.info/sct | Semantic dementia (disorder) |
230289009 | http://snomed.info/sct | Patchy dementia (disorder) |
231536004 | http://snomed.info/sct | Atypical autism (disorder) |
23560001 | http://snomed.info/sct | Asperger's disorder (disorder) |
2421000119107 | http://snomed.info/sct | Hallucinations co-occurrent and due to late onset dementia (disorder) |
25772007 | http://snomed.info/sct | Multi-infarct dementia with delusions (disorder) |
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) |
278857002 | http://snomed.info/sct | Dementia of frontal lobe type (disorder) |
281004 | http://snomed.info/sct | Dementia associated with alcoholism (disorder) |
288631000119104 | http://snomed.info/sct | Vascular dementia with behavioral disturbance (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) |
32875003 | http://snomed.info/sct | Inhalant-induced persisting dementia (disorder) |
33982008 | http://snomed.info/sct | Hyperphosphatasemia with intellectual disability (disorder) |
35919005 | http://snomed.info/sct | Pervasive developmental disorder (disorder) |
371024007 | http://snomed.info/sct | Senile dementia with delusion (disorder) |
371026009 | http://snomed.info/sct | Senile dementia with psychosis (disorder) |
373618009 | http://snomed.info/sct | Autistic spectrum disorder with isolated skills (disorder) |
39951000119105 | http://snomed.info/sct | Pervasive developmental disorder of residual state (disorder) |
40700009 | http://snomed.info/sct | Severe intellectual disability (disorder) |
408856003 | http://snomed.info/sct | Autistic disorder (disorder) |
408857007 | http://snomed.info/sct | Infantile autism (disorder) |
412787009 | http://snomed.info/sct | Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth (disorder) |
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) |
420614009 | http://snomed.info/sct | Organic dementia with acquired immunodeficiency syndrome (disorder) |
421023003 | http://snomed.info/sct | Presenile dementia with acquired immunodeficiency syndrome (disorder) |
421529006 | http://snomed.info/sct | Dementia with acquired immunodeficiency syndrome (disorder) |
422437002 | http://snomed.info/sct | X-linked intellectual disability with marfanoid habitus (disorder) |
425390006 | http://snomed.info/sct | Dementia associated with Parkinson's Disease (disorder) |
428051000124108 | http://snomed.info/sct | Mild dementia (disorder) |
428351000124105 | http://snomed.info/sct | Severe dementia (disorder) |
429161000124103 | http://snomed.info/sct | Primary degenerative dementia of the Alzheimer type, senile onset, with behavioral disturbance (disorder) |
429458009 | http://snomed.info/sct | Dementia due to Creutzfeldt Jakob disease (disorder) |
429998004 | http://snomed.info/sct | Vascular dementia (disorder) |
430771000124100 | http://snomed.info/sct | Moderate dementia (disorder) |
432091002 | http://snomed.info/sct | Savant syndrome (disorder) |
43614003 | http://snomed.info/sct | Autistic disorder of childhood onset (disorder) |
442314000 | http://snomed.info/sct | Active but odd autism (disorder) |
442344002 | http://snomed.info/sct | Dementia due to Huntington chorea (disorder) |
4817008 | http://snomed.info/sct | Primary degenerative dementia of the Alzheimer type, senile onset, with delirium (disorder) |
51928006 | http://snomed.info/sct | General paresis - neurosyphilis (disorder) |
52448006 | http://snomed.info/sct | Dementia (disorder) |
54502004 | http://snomed.info/sct | Primary degenerative dementia of the Alzheimer type, presenile onset, with delusions (disorder) |
55009008 | http://snomed.info/sct | Primary degenerative dementia of the Alzheimer type, senile onset, with delusions (disorder) |
56267009 | http://snomed.info/sct | Multi-infarct dementia (disorder) |
59651006 | http://snomed.info/sct | Sedative, hypnotic AND/OR anxiolytic-induced persisting dementia (disorder) |
61152003 | http://snomed.info/sct | Moderate intellectual disability (disorder) |
6475002 | http://snomed.info/sct | Primary degenerative dementia of the Alzheimer type, presenile onset, uncomplicated (disorder) |
65096006 | http://snomed.info/sct | Primary degenerative dementia of the Alzheimer type, presenile onset, with delirium (disorder) |
66108005 | http://snomed.info/sct | Primary degenerative dementia of the Alzheimer type, senile onset, uncomplicated (disorder) |
68618008 | http://snomed.info/sct | Rett's disorder (disorder) |
698624003 | http://snomed.info/sct | Dementia associated with cerebral lipidosis (disorder) |
698625002 | http://snomed.info/sct | Dementia associated with normal pressure hydrocephalus (disorder) |
698626001 | http://snomed.info/sct | Dementia associated with multiple sclerosis (disorder) |
698725008 | http://snomed.info/sct | Dementia associated with neurosyphilis (disorder) |
698726009 | http://snomed.info/sct | Dementia associated with viral encephalitis (disorder) |
698781002 | http://snomed.info/sct | Dementia associated with cerebral anoxia (disorder) |
698948009 | http://snomed.info/sct | Vascular dementia in remission (disorder) |
698949001 | http://snomed.info/sct | Dementia in remission (disorder) |
698954005 | http://snomed.info/sct | Primary degenerative dementia of the Alzheimer type, senile onset in remission (disorder) |
698955006 | http://snomed.info/sct | Primary degenerative dementia of the Alzheimer type, presenile onset in remission (disorder) |
699297004 | http://snomed.info/sct | Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type (disorder) |
702356009 | http://snomed.info/sct | X-linked intellectual disability-psychosis-macroorchidism syndrome (disorder) |
702393003 | http://snomed.info/sct | Frontotemporal dementia with gene located on 3p11 (disorder) |
702416008 | http://snomed.info/sct | X-linked intellectual disability Snyder type (disorder) |
702450004 | http://snomed.info/sct | FOXG1 syndrome (disorder) |
702732007 | http://snomed.info/sct | High-functioning autism (disorder) |
703389002 | http://snomed.info/sct | Calcium/calmodulin-dependent serine protein kinase related intellectual disability (disorder) |
703526007 | http://snomed.info/sct | Progressive epilepsy-intellectual disability syndrome Finnish type (disorder) |
708037001 | http://snomed.info/sct | Residual Asperger's disorder (disorder) |
70936005 | http://snomed.info/sct | Multi-infarct dementia, uncomplicated (disorder) |
712884004 | http://snomed.info/sct | Pathological demand avoidance (disorder) |
713488003 | http://snomed.info/sct | Presenile dementia co-occurrent with human immunodeficiency virus infection (disorder) |
713844000 | http://snomed.info/sct | Dementia co-occurrent with human immunodeficiency virus infection (disorder) |
715342005 | http://snomed.info/sct | Alpha thalassemia X-linked intellectual disability syndrome (disorder) |
715628009 | http://snomed.info/sct | Intellectual disability, truncal obesity, retinal dystrophy and micropenis syndrome (disorder) |
715737004 | http://snomed.info/sct | Parkinsonism co-occurrent with dementia of Guadeloupe (disorder) |
715989002 | http://snomed.info/sct | Congenital cataract with intellectual disability and anal atresia and urinary defect syndrome (disorder) |
716024001 | http://snomed.info/sct | Goniodysgenesis with intellectual disability and short stature syndrome (disorder) |
716096005 | http://snomed.info/sct | Hypospadias and intellectual disability syndrome Goldblatt type (disorder) |
716107009 | http://snomed.info/sct | Early onset parkinsonism and intellectual disability syndrome (disorder) |
716112005 | http://snomed.info/sct | Microcephaly with deafness and intellectual disability syndrome (disorder) |
716191002 | http://snomed.info/sct | Alopecia and intellectual disability syndrome (disorder) |
716334004 | http://snomed.info/sct | Intellectual disability and short stature with hand contracture and genital anomaly syndrome (disorder) |
716667005 | http://snomed.info/sct | Right temporal atrophy variant frontotemporal dementia (disorder) |
716706009 | http://snomed.info/sct | Female restricted epilepsy with intellectual disability syndrome (disorder) |
716709002 | http://snomed.info/sct | FRAXE intellectual disability syndrome (disorder) |
716994006 | http://snomed.info/sct | Behavioral variant of frontotemporal dementia (disorder) |
717222003 | http://snomed.info/sct | Microphthalmia with ankyloblepharon and intellectual disability syndrome (disorder) |
718393002 | http://snomed.info/sct | Atypical Rett syndrome (disorder) |
718577005 | http://snomed.info/sct | X-linked intellectual disability Atkin type (disorder) |
718766002 | http://snomed.info/sct | Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome (disorder) |
718845002 | http://snomed.info/sct | X-linked intellectual disability with ataxia and apraxia syndrome (disorder) |
718896000 | http://snomed.info/sct | X-linked recessive intellectual disability and macrocephaly with ciliary dysfunction syndrome (disorder) |
718897009 | http://snomed.info/sct | X-linked intellectual disability Seemanova type (disorder) |
718900002 | http://snomed.info/sct | Syndromic X-linked intellectual disability type 11 (disorder) |
718905007 | http://snomed.info/sct | X-linked intellectual disability Shrimpton type (disorder) |
718908009 | http://snomed.info/sct | X-linked intellectual disability Siderius type (disorder) |
718909001 | http://snomed.info/sct | X-linked intellectual disability Stevenson type (disorder) |
718910006 | http://snomed.info/sct | X-linked intellectual disability Stocco Dos Santos type (disorder) |
718911005 | http://snomed.info/sct | X-linked intellectual disability Stoll type (disorder) |
718912003 | http://snomed.info/sct | X-linked intellectual disability Turner type (disorder) |
718914002 | http://snomed.info/sct | X-linked intellectual disability Van Esch type (disorder) |
719009006 | http://snomed.info/sct | X-linked intellectual disability Wilson type (disorder) |
719010001 | http://snomed.info/sct | X-linked intellectual disability Schimke type (disorder) |
719011002 | http://snomed.info/sct | X-linked intellectual disability Pai type (disorder) |
719012009 | http://snomed.info/sct | X-linked intellectual disability Miles Carpenter type (disorder) |
719013004 | http://snomed.info/sct | X-linked intellectual disability Cilliers type (disorder) |
719016007 | http://snomed.info/sct | X-linked intellectual disability Cantagrel type (disorder) |
719017003 | http://snomed.info/sct | X-linked intellectual disability Armfield type (disorder) |
719018008 | http://snomed.info/sct | X-linked intellectual disability Abidi type (disorder) |
719042007 | http://snomed.info/sct | Uveal coloboma with cleft lip and palate and intellectual disability syndrome (disorder) |
719136005 | http://snomed.info/sct | X-linked intellectual disability with cerebellar hypoplasia syndrome (disorder) |
719138006 | http://snomed.info/sct | X-linked intellectual disability with cubitus valgus and dysmorphism syndrome (disorder) |
719139003 | http://snomed.info/sct | X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizure syndrome (disorder) |
719140001 | http://snomed.info/sct | X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) |
719155005 | http://snomed.info/sct | X-linked intellectual disability and epilepsy with progressive joint contracture and facial dysmorphism syndrome (disorder) |
719156006 | http://snomed.info/sct | X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome (disorder) |
719157002 | http://snomed.info/sct | X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome (disorder) |
719160009 | http://snomed.info/sct | Syndromic X-linked intellectual disability type 7 (disorder) |
719161008 | http://snomed.info/sct | Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation (disorder) |
719256004 | http://snomed.info/sct | Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) |
719450007 | http://snomed.info/sct | Disorder of sex development with intellectual disability syndrome (disorder) |
719600006 | http://snomed.info/sct | 1p21.3 microdeletion syndrome (disorder) |
71961003 | http://snomed.info/sct | Childhood disintegrative disorder (disorder) |
719800009 | http://snomed.info/sct | Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (disorder) |
719810000 | http://snomed.info/sct | X-linked intellectual disability with seizure and psoriasis syndrome (disorder) |
719811001 | http://snomed.info/sct | X-linked intellectual disability Cabezas type (disorder) |
719812008 | http://snomed.info/sct | X-linked intellectual disability with plagiocephaly syndrome (disorder) |
719825000 | http://snomed.info/sct | X-linked intellectual disability, macrocephaly, macroorchidism syndrome (disorder) |
719826004 | http://snomed.info/sct | X-linked intellectual disability with acromegaly and hyperactivity syndrome (disorder) |
719842006 | http://snomed.info/sct | Congenital hypoplasia of ulna and intellectual disability syndrome (disorder) |
720468000 | http://snomed.info/sct | Aniridia and intellectual disability syndrome (disorder) |
720501007 | http://snomed.info/sct | Arachnodactyly with abnormal ossification and intellectual disability syndrome (disorder) |
720502000 | http://snomed.info/sct | Arachnodactyly and intellectual disability with facial dysmorphism syndrome (disorder) |
720517001 | http://snomed.info/sct | Ataxia with deafness and intellectual disability syndrome (disorder) |
720639008 | http://snomed.info/sct | Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome (disorder) |
720748007 | http://snomed.info/sct | Aural atresia with multiple congenital anomalies and intellectual disability syndrome (disorder) |
720979002 | http://snomed.info/sct | Alopecia, contracture, dwarfism, intellectual disability syndrome (disorder) |
720980004 | http://snomed.info/sct | Alopecia, psychomotor epilepsy, periodontal pyorrhea, intellectual disability syndrome (disorder) |
720981000 | http://snomed.info/sct | Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) |
720982007 | http://snomed.info/sct | Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (disorder) |
720987001 | http://snomed.info/sct | Aniridia, ptosis, intellectual disability, familial obesity syndrome (disorder) |
721007005 | http://snomed.info/sct | Hair defect with photosensitivity and intellectual disability syndrome (disorder) |
721017000 | http://snomed.info/sct | Postaxial polydactyly and intellectual disability syndrome (disorder) |
721087008 | http://snomed.info/sct | Deafness and intellectual disability Martin Probst type syndrome (disorder) |
721089006 | http://snomed.info/sct | Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome (disorder) |
721146009 | http://snomed.info/sct | Intellectual disability, epilepsy, bulbous nose syndrome (disorder) |
721207002 | http://snomed.info/sct | Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome (disorder) |
721841001 | http://snomed.info/sct | Hypogonadism with mitral valve prolapse and intellectual disability syndrome (disorder) |
721973006 | http://snomed.info/sct | Lipodystrophy, intellectual disability, deafness syndrome (disorder) |
722002002 | http://snomed.info/sct | Intellectual disability, balding, patella luxation, acromicria syndrome (disorder) |
722003007 | http://snomed.info/sct | Intellectual disability with cataract and kyphosis syndrome (disorder) |
722035007 | http://snomed.info/sct | Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome (disorder) |
722037004 | http://snomed.info/sct | Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome (disorder) |
722110003 | http://snomed.info/sct | Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome (disorder) |
722209002 | http://snomed.info/sct | Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (disorder) |
722213009 | http://snomed.info/sct | Severe X-linked intellectual disability Gustavson type (disorder) |
722282008 | http://snomed.info/sct | Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome (disorder) |
722287002 | http://snomed.info/sct | Autism and facial port-wine stain syndrome (disorder) |
722379001 | http://snomed.info/sct | Congenital cataract with hypertrichosis and intellectual disability syndrome (disorder) |
722380003 | http://snomed.info/sct | Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome (disorder) |
722454003 | http://snomed.info/sct | Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome (disorder) |
722455002 | http://snomed.info/sct | Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome (disorder) |
722456001 | http://snomed.info/sct | Intellectual disability, developmental delay, contracture syndrome (disorder) |
722459008 | http://snomed.info/sct | Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) |
722478008 | http://snomed.info/sct | Skeletal dysplasia with intellectual disability syndrome (disorder) |
722600006 | http://snomed.info/sct | Non-amnestic Alzheimer disease (disorder) |
722977005 | http://snomed.info/sct | Dementia co-occurrent and due to neurocysticercosis (disorder) |
722978000 | http://snomed.info/sct | Dementia caused by toxin (disorder) |
722979008 | http://snomed.info/sct | Dementia due to metabolic abnormality (disorder) |
722980006 | http://snomed.info/sct | Dementia due to chromosomal anomaly (disorder) |
723123001 | http://snomed.info/sct | Ischemic vascular dementia (disorder) |
723304001 | http://snomed.info/sct | Microcephaly, seizure, intellectual disability, heart disease syndrome (disorder) |
723332005 | http://snomed.info/sct | Isodicentric chromosome 15 syndrome (disorder) |
723336008 | http://snomed.info/sct | Fallot complex with intellectual disability and growth delay syndrome (disorder) |
723365002 | http://snomed.info/sct | Hypotrichosis and intellectual disability syndrome Lopes type (disorder) |
723390000 | http://snomed.info/sct | Rapidly progressive dementia (disorder) |
723441001 | http://snomed.info/sct | Non-progressive cerebellar ataxia with intellectual disability (disorder) |
723621000 | http://snomed.info/sct | Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome (disorder) |
723676007 | http://snomed.info/sct | Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome (disorder) |
723994004 | http://snomed.info/sct | Seizures and intellectual disability due to hydroxylysinuria syndrome (disorder) |
724001005 | http://snomed.info/sct | Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) |
724178000 | http://snomed.info/sct | Laryngeal abductor paralysis with intellectual disability syndrome (disorder) |
724776007 | http://snomed.info/sct | Dementia due to disorder of central nervous system (disorder) |
724777003 | http://snomed.info/sct | Dementia due to infectious disease (disorder) |
724992007 | http://snomed.info/sct | Epilepsy co-occurrent and due to dementia (disorder) |
725163002 | http://snomed.info/sct | X-linked spasticity, intellectual disability, epilepsy syndrome (disorder) |
725898002 | http://snomed.info/sct | Delirium co-occurrent with dementia (disorder) |
725906006 | http://snomed.info/sct | Intellectual disability Buenos Aires type (disorder) |
725912001 | http://snomed.info/sct | X-linked intellectual disability Brooks type (disorder) |
726031001 | http://snomed.info/sct | Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) |
726709001 | http://snomed.info/sct | Intellectual disability, cataract, calcified pinna, myopathy syndrome (disorder) |
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) |
732961003 | http://snomed.info/sct | Branchial dysplasia, intellectual disability, inguinal hernia syndrome (disorder) |
733062000 | http://snomed.info/sct | Marfanoid habitus with autosomal recessive intellectual disability 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) |
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) |
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) |
733469003 | http://snomed.info/sct | Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome (disorder) |
733522005 | http://snomed.info/sct | Megalocornea with intellectual disability syndrome (disorder) |
733623005 | http://snomed.info/sct | Autism spectrum disorder, epilepsy, arthrogryposis syndrome (disorder) |
734017008 | http://snomed.info/sct | Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
734349003 | http://snomed.info/sct | Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) |
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) |
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) |
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) |
763626009 | http://snomed.info/sct | Intellectual disability due to nutritional deficiency (disorder) |
763665007 | http://snomed.info/sct | Craniodigital syndrome and intellectual disability 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) |
763861000 | http://snomed.info/sct | Pachygyria, intellectual disability, epilepsy 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) |
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) |
765761009 | http://snomed.info/sct | Brachydactyly, mesomelia, intellectual disability, heart defect syndrome (disorder) |
766824003 | http://snomed.info/sct | Activity dependent neuroprotector homeobox related multiple congenital anomalies, intellectual disability, autism spectrum disorder (disorder) |
768677000 | http://snomed.info/sct | Protein phosphatase 2 regulatory subunit b (b56) delta-related intellectual disability (disorder) |
768843007 | http://snomed.info/sct | Tall stature, intellectual disability, facial dysmorphism 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) |
770679002 | http://snomed.info/sct | Polyneuropathy, intellectual disability, acromicria, premature menopause 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) |
770750002 | http://snomed.info/sct | Intellectual disability, seizures, macrocephaly, obesity syndrome (disorder) |
770755007 | http://snomed.info/sct | Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome (disorder) |
770790004 | http://snomed.info/sct | Developmental delay with autism spectrum disorder and gait instability (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) |
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) |
771448004 | http://snomed.info/sct | Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency (disorder) |
771512003 | http://snomed.info/sct | Autism spectrum disorder due to AUTS2 activator of transcription and developmental regulator deficiency (disorder) |
77287004 | http://snomed.info/sct | Borderline intellectual disability (disorder) |
773274001 | http://snomed.info/sct | X-linked intellectual disability, craniofacioskeletal 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) |
773419004 | http://snomed.info/sct | Severe intellectual disability, short stature, behavioral abnormalities, facial dysmorphism syndrome (disorder) |
773498006 | http://snomed.info/sct | Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency (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) |
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) |
773692000 | http://snomed.info/sct | Late-onset localized junctional epidermolysis bullosa, intellectual disability syndrome (disorder) |
773772001 | http://snomed.info/sct | Rare non-syndromic intellectual disability (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) |
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) |
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) |
780827006 | http://snomed.info/sct | Synaptic Ras GTPase activating protein 1- related intellectual disability (disorder) |
782721009 | http://snomed.info/sct | Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUN and cysteine rich domain containing beclin 1 interacting protein deficiency (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) |
782772000 | http://snomed.info/sct | Congenital muscular dystrophy with intellectual disability and severe epilepsy (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) |
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) |
783175003 | http://snomed.info/sct | Congenital muscular dystrophy without 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) |
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) |
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) |
816067005 | http://snomed.info/sct | Diabetes, hypogonadism, deafness, intellectual disability syndrome (disorder) |
82351000119105 | http://snomed.info/sct | Altered behavior due to Pick's disease (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) |
840464007 | http://snomed.info/sct | Dementia due to carbon monoxide poisoning (disorder) |
840465008 | http://snomed.info/sct | Dementia due to iron deficiency (disorder) |
86765009 | http://snomed.info/sct | Mild intellectual disability (disorder) |
870260008 | http://snomed.info/sct | Pervasive developmental disorder with marked impairment of functional language with loss of previously acquired skills (disorder) |
870261007 | http://snomed.info/sct | Pervasive developmental disorder with marked impairment of functional language without loss of previously acquired skills (disorder) |
870262000 | http://snomed.info/sct | Pervasive developmental disorder with disorder of intellectual development without loss of previously acquired skills (disorder) |
870263005 | http://snomed.info/sct | Pervasive developmental disorder with impairment of functional language (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) |
870280009 | http://snomed.info/sct | Pervasive developmental disorder with severe impairment of functional language with loss of previously acquired skills (disorder) |
870282001 | http://snomed.info/sct | Pervasive developmental disorder with severe impairment of functional language without loss of previously acquired skills (disorder) |
870303005 | http://snomed.info/sct | Pervasive developmental disorder with complete impairment of functional language with loss of previously acquired skills (disorder) |
870304004 | http://snomed.info/sct | Pervasive developmental disorder with complete impairment of functional language without 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) |
870306002 | http://snomed.info/sct | Pervasive developmental disorder with complete impairment of functional language (disorder) |
870307006 | http://snomed.info/sct | Pervasive developmental disorder with abscence of functional language (disorder) |
870308001 | http://snomed.info/sct | Pervasive developmental disorder with cognitive developmental delay and complete impairment of functional language (disorder) |
90099008 | http://snomed.info/sct | Subcortical leukoencephalopathy (disorder) |
9345005 | http://snomed.info/sct | Dialysis dementia (disorder) |
97751000119108 | http://snomed.info/sct | Altered behavior in Alzheimer's disease (disorder) |
Produced 08 Sep 2023