cognitive-impairment
Metadata
- Coding system
- SNOMED CT (UK Clinical Edition)
- Coding system release
- 42.4.0
- Organisation
- OpenSAFELY
- Codelist ID
- opensafely/cognitive-impairment
- Version ID
- 4c1e80f3
- Number of codes included
- 203
About
Description
This codelists identifies individuals with probable cognitive impairment for dementia/ shingles vaccine study.
The purpose is to identify those who are on "dementia trajectory" to stratify the effect of the vaccine on dementia incidence.
Methodology
Context
Dementia/ shingles vaccine study - to identify those on "dementia trajectory" for sensitivity analyses.
Inclusion/exclusion criteria
Inclusion: Codes indicating a diagnosis of cognitive impairment Codes indicating a history of diagnosis of cognitive impairment
Exclusion: Administrative codes relating to memory clinic referrals or memory tests/ assessments Codes indicating resolution of memory difficulties Codes indicating established dementia Symptoms of cognitive dysfunction, not related to or more likely to be used in context other than cognitive impairment
Borderline cases
Codes indicating memory difficulties/ abnormalities which are often assessed in the context of suspected cognitive impairment (e.g. does not remember date of birth) - this increases sensitivity Administrative codes indicating that a diagnosis of cognitive impairment is present (e.g. mild cognitive impairment review - first invitation letter). General amnesia codes included as long as not in the context of other clinical condition (such as post-traumatic amnesia).
Sensitivity vs specificity
The codelist is sensitive and includes cognition and memory difficulties indicative of cognitive impairment, rather than only the codes indicating a formal diagnosis. Cognition difficulties likely to be recorded in other clinical contexts (e.g. autism) are excluded.
Additional information
See Github issue.
References
Signed off by
- Arina Tamborska, (Sept. 2, 2026)
Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.
We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.
| code | term |
|---|---|
| 102891000 | Age-related cognitive decline |
| 1034921000000105 | Memory: months of year in reverse unsuccessful |
| 1034931000000107 | Memory: months of year in reverse unsuccessful |
| 1036821000000108 | Mild cognitive impairment review invitation |
| 1036841000000101 | Mild cognitive impairment review invitation first letter |
| 1036861000000100 | Mild cognitive impairment review invitation second letter |
| 1036881000000109 | Mild cognitive impairment review invitation third letter |
| 1047041000000108 | Mild cognitive impairment review |
| 1052381000000103 | Mild cognitive impairment annual review |
| 1068921000000107 | Difficulty recognising familiar people |
| 1068951000000102 | Difficulty remembering places |
| 1069171000000103 | Does not recognise objects by touch |
| 1069191000000104 | Does not remember routines |
| 1070761000000109 | Difficulty recognising objects |
| 1070771000000102 | Difficulty recognising objects by sight |
| 1070781000000100 | Difficulty recognising objects by touch |
| 1070801000000104 | Difficulty recognising surroundings |
| 1070821000000108 | Difficulty remembering past events |
| 1070831000000105 | Difficulty remembering people |
| 1070841000000101 | Difficulty remembering routines |
| 1072411000000103 | Does not recognise familiar people |
| 1072451000000104 | Does not recognise objects |
| 1072461000000101 | Does not recognise objects by sight |
| 1072491000000107 | Does not recognise surroundings |
| 1072501000000101 | Does not remember past events |
| 1072511000000104 | Does not remember people |
| 1072521000000105 | Does not remember places |
| 1075681000000104 | Unable to remember past events |
| 1075691000000102 | Unable to remember people |
| 1075701000000102 | Unable to remember places |
| 1075711000000100 | Unable to remember routines |
| 110352000 | Minimal cognitive impairment |
| 110355003 | Lack of thinking ability |
| 111481000000100 | Poor visual sequential memory |
| 111491000000103 | Poor auditory sequential memory |
| 116340000 | Disturbance of cognitive learning |
| 117931000000104 | Poor visual sequential memory |
| 117941000000108 | Poor auditory sequential memory |
| 1186839009 | Cognitive impairment due to lead toxicity |
| 1234774002 | Cognitive impairment caused by ethanol |
| 1259562009 | Cognitive impairment due to late-delayed irradiation of brain |
| 1303576005 | Forgets to take medication |
| 130964008 | Impaired environmental interpretation syndrome |
| 130988005 | Chronic confusion |
| 1386319000 | Digit span forwards performance impaired |
| 1386320006 | Digit span reverse performance impaired |
| 139484009 | Memory disturbance (& amnesia (& symptom)) |
| 140621000119106 | Memory disorder co-occurrent and due to organic brain damage |
| 140826008 | Mild cognitive disorder |
| 140828009 | Forgetful |
| 141601000119107 | Cognitive changes due to organic disorder |
| 142261000119100 | Cognitive deficit in attention |
| 142281000119109 | Cognitive deficit in visuospatial function |
| 142291000119107 | Cognitive deficit in psychomotor function |
| 142689007 | Memory: own age not known |
| 142692006 | Memory: present time not known |
| 142695008 | Memory: present place not knwn |
| 142698005 | Memory: present year not known |
| 142701002 | Memory: own DOB not known |
| 142704005 | Memory: present month not knwn |
| 142707003 | Memory: important event not kn |
| 142710005 | Memory: import.person not knwn |
| 142715000 | Memory: count down unsuccess. |
| 142718003 | Memory: address recall unsucc. |
| 145040006 | Mild cognitive disorder |
| 154961004 | Memory disturbance: [mild] |
| 158178004 | [D]Amnesia (retrograde) |
| 15928141000119107 | Cognitive impairment co-occurrent and due to human immunodeficiency virus infection |
| 162199006 | Memory disturbance (& amnesia (& symptom)) |
| 163619002 | Mild cognitive disorder |
| 163621007 | Forgetful |
| 165280004 | Memory: own age not known |
| 165283002 | Memory: present time not known |
| 165286005 | Memory: present place not known |
| 165289003 | Memory: present year not known |
| 165292004 | Memory: own date of birth not known |
| 165295002 | Memory: present month not known |
| 165298000 | Memory: important event not known |
| 165301001 | Memory: important person not known |
| 165305005 | Memory: count down unsuccessful |
| 165308007 | Memory: address recall unsuccessful |
| 16703491000119101 | Memory deficit due to and following spontaneous intracerebral hemorrhage |
| 16703551000119107 | Memory deficit due to and following cerebrovascular disease |
| 16703601000119109 | Memory deficit due to and following spontaneous subarachnoid hemorrhage |
| 16703661000119105 | Memory deficit due to and following cerebrovascular accident |
| 16703711000119100 | Memory deficit due to and following embolic cerebrovascular accident |
| 16703761000119102 | Memory deficit due to and following ischemic cerebrovascular accident |
| 16703821000119101 | Memory deficit due to and following hemorrhagic cerebrovascular accident |
| 186561000000101 | Disturbance of memory for order of events |
| 190001000000109 | Disturbance of memory for order of events |
| 191520004 | Chronic confusional state |
| 192071009 | Mild memory disturbance |
| 192072002 | Organic memory impairment |
| 192195008 | Mild cognitive disorder |
| 206784007 | [D]Amnesia (retrograde) |
| 206789002 | [D]Anterograde amnesia |
| 207606006 | [X]Other amnesia |
| 225037001 | Minor memory lapses |
| 225038006 | Memory lapses |
| 225039003 | Mixes past with present |
| 229676007 | Language-related cognitive disorder |
| 231447009 | Mild cognitive disorder |
| 231448004 | Age-associated memory impairment |
| 247588002 | Poor long-term memory |
| 247592009 | Poor short-term memory |
| 247593004 | Forgets what was going to do |
| 247594005 | Forgets what was going to say |
| 247595006 | Forgets recent activities |
| 247596007 | Forgets what has just done |
| 247597003 | Forgets what has just said |
| 247598008 | Forgets what has just read |
| 247599000 | Forgets what has just seen |
| 247600002 | Forgets what has just heard |
| 247606008 | Amnesia |
| 247607004 | Amnesia for day to day facts |
| 247608009 | Unable to remember today's date |
| 247609001 | Unable to remember name of reigning monarch |
| 247610006 | Unable to remember name of current prime minister |
| 247611005 | Amnesia for important personal information |
| 247612003 | Cannot remember names of intimates |
| 247613008 | Unable to remember own age |
| 247614002 | Cannot remember wedding anniversary |
| 247615001 | Cannot remember birth dates of children |
| 247616000 | Cannot remember name of school |
| 268792003 | Memory disturbance: [mild] |
| 275278005 | Difficulty in remembering dates |
| 280994000 | Chronic confusional state |
| 283878007 | Impairment of registration |
| 283902008 | Has delayed recall |
| 285157008 | Unable to recognize objects |
| 285161002 | Unable to recognize objects by touch |
| 285164005 | Unable to recognize objects by sight |
| 285169000 | Unable to recognize faces by sight |
| 285171000 | Unable to recognize faces |
| 285177001 | Unable to recognize surroundings |
| 285188007 | Unable to remember own date of birth |
| 285191007 | Unable to remember day of the week |
| 285194004 | Unable to remember month of year |
| 285197006 | Unable to remember current year |
| 285208000 | Unable to recall random address at five minutes |
| 285210003 | Unable to reproduce geometric figure at five minutes |
| 285212006 | Unable to recall five digit number at five minutes |
| 285219002 | Unable to remember motor skills |
| 285221007 | Unable to remember new motor skills |
| 285223005 | Unable to remember old motor skills |
| 285225003 | Unable to remember objects |
| 285228001 | Unable to remember faces |
| 285230004 | Unable to remember sounds |
| 285774001 | Unable to recognize familiar people |
| 290621000119101 | Cognitive deficit due to and following cerebrovascular disease |
| 291621000119109 | Cognitive deficit due to and following nontraumatic subarachnoid hemorrhage |
| 291711000119109 | Cognitive deficit due to and following nontraumatic intracerebral hemorrhage |
| 311533004 | Delayed verbal memory |
| 33254005 | Uncompensated short term memory deficit |
| 386805003 | Mild neurocognitive disorder |
| 386806002 | Impaired cognition |
| 386807006 | Memory impairment |
| 41171000000106 | Mild cognitive disorder |
| 413088002 | Poor visual sequential memory |
| 413089005 | Poor auditory sequential memory |
| 42176003 | Amnesia for recent events |
| 423864004 | Forgets to complete personal care |
| 433081000 | Organic amnesia of language |
| 442212003 | Residual cognitive deficit as late effect of cerebrovascular accident |
| 443265004 | Cognitive disorder |
| 454161000124103 | Noncompliance with medication regimen due to cognitive impairment |
| 480201000000101 | [X]Other amnesia |
| 48167000 | Amnesia |
| 495901000000102 | [D]Amnesia (retrograde) |
| 495941000000104 | [D]Anterograde amnesia |
| 51921000 | Retrograde amnesia |
| 55261000087107 | Neurocognitive disorder suspected |
| 55533009 | Forgetful |
| 6149008 | Amnesia for remote events |
| 672561000119103 | Cognitive deficit due to and following ischemic cerebrovascular accident |
| 672571000119109 | Cognitive deficit due to and following hemorrhagic cerebrovascular accident |
| 690341000119100 | Cognitive deficit due to and following embolic cerebrovascular accident |
| 698691002 | Cognitive disorder in remission |
| 702955000 | Moderate cognitive impairment |
| 702956004 | Severe cognitive impairment |
| 709073001 | Neurocognitive disorder |
| 716306006 | Acquired language comprehension impairment |
| 716635007 | Cognitive communication disorder |
| 724760003 | Cognitive impairment co-occurrent and due to primary psychotic disorder |
| 736317001 | Impaired executive functioning |
| 762298000 | Cognitive impairment due to toxicity of substance |
| 76789006 | Information conversion problem |
| 771417007 | Cognitive dysfunction following surgical procedure |
| 78461004 | Memory impairment |
| 78521000000105 | Mild cognitive disorder |
| 80216008 | Impaired cognition |
| 808311000000102 | Poor short-term memory |
| 836301008 | Amnestic mild cognitive disorder |
| 85173004 | False recognition |
| 88822006 | Anterograde amnesia |
| 888271000000101 | Mild cognitive impairment |
| 888281000000104 | Mild cognitive impairment |
| 888291000000102 | Moderate cognitive impairment |
| 888301000000103 | Moderate cognitive impairment |
| 888311000000101 | Severe cognitive impairment |
| 888321000000107 | Severe cognitive impairment |
| 918271000000105 | Impaired cognition |
| 990531000000107 | Memory impairment |
This page shows the search terms that were used to build the codelist. Concepts that match the search terms, but which were excluded, are in faint grey.
Chronic confusion
Included 3 out of 3 matching concepts.
Show matching concepts
-
Chronic confusion (
130988005) -
Chronic confusional state (
191520004) -
Chronic confusional state (
280994000)
amnesia
Included 18 out of 55 matching concepts.
Show matching concepts
-
Alexia (
9236007) -
Amnesia (
48167000) -
Amnesia (
247606008) -
Amnesia for day to day facts (
247607004) -
Amnesia for important personal information (
247611005) -
Amnesia for recent events (
42176003) -
Amnesia for remote events (
6149008) -
Anterograde amnesia (
88822006) -
Assessment using Galveston Orientation and Amnesia Test (
715810009) -
Assessment using Galveston Orientation and Amnesia Test (
966451000000104) -
Assessment using Westmead Post-Traumatic Amnesia Scale (
980521000000109) -
Assessment using Westmead Post-Traumatic Amnesia scale (
716093002) -
Dissociative amnesia (
84209002) -
Dissociative amnesia (
192420000) -
Dissociative amnesia (
191716000) -
Family history of amnesia (
430728001) -
Galveston Orientation and Amnesia Test score (
720207005) -
Galveston Orientation and Amnesia Test score (
968571000000108) -
Galveston orientation and amnesia test (
273474006) -
Hysterical amnesia (
16039007) -
Incomplete loss of consciousness without amnesia (
735662004) -
Induction of amnesia (
442944005) -
Localized dissociative amnesia (
225040001) -
Memory disturbance (& amnesia (& symptom)) (
139484009) -
Memory disturbance (& amnesia (& symptom)) (
162199006) -
Musical alexia (
16170002) -
Organic amnesia of language (
433081000) -
Paramnesia (
32541007) -
Post-traumatic amnesia (
275277000) -
Posttraumatic amnesia (
85970000) -
Psychoactive substance-induced organic amnestic disorder (
83168008) -
Retrograde amnesia (
51921000) -
Tactile agnosia (
25094008) -
Temporary amnesia (
89051002) -
Temporary loss of memory (
162200009) -
Tolerance, Worry, Eye-opener, Amnesia, K/Cut down questionnaire (
568241000005104) -
Tolerance, Worry, Eye-opener, Amnesia, K/Cut down questionnaire score (
568251000005102) -
Transient epileptic amnesia (
395689002) -
Transient epileptic amnesia (
395609000) -
Transient epileptic amnesia (
395563009) -
Transient global amnesia (
230736007) -
Transient global amnesia (
367187006) -
Transient global amnesia (
366963000) -
Transient global amnesia (
195202003) -
Transient memory loss (
307413004) -
Westmead Post-Traumatic Amnesia Scale (
273928003) -
Westmead Post-Traumatic Amnesia Scale score (
980531000000106) -
Westmead Post-traumatic Amnesia Scale score (
717323005) -
[D]Amnesia (retrograde) (
206784007) -
[D]Amnesia (retrograde) (
495901000000102) -
[D]Amnesia (retrograde) (
158178004) -
[D]Anterograde amnesia (
495941000000104) -
[D]Anterograde amnesia (
206789002) -
[X]Other amnesia (
480201000000101) -
[X]Other amnesia (
207606006)
cognition
Included 81 out of 1094 matching concepts.
Show matching concepts
-
11p15.4 microduplication syndrome (
770794008) -
11q22.2q22.3 microdeletion syndrome (
1229882003) -
12p12.1 microdeletion syndrome (
778007004) -
12q14 microdeletion syndrome (
719046005) -
13q12.3 microdeletion syndrome (
773547003) -
14q24.1q24.3 microdeletion syndrome (
773494008) -
15q overgrowth syndrome (
771477003) -
17q11.2 microduplication syndrome (
719583002) -
17q24.2 microdeletion syndrome (
1229873009) -
19p13.3 microduplication syndrome (
1229883008) -
19q13.11 microdeletion syndrome (
719599008) -
1p21.3 microdeletion syndrome (
719600006) -
20q11.2 microdeletion syndrome (
1229891004) -
21q22.11q22.12 microdeletion syndrome (
787171006) -
2p13.2 microdeletion syndrome (
770756008) -
2p21 microdeletion syndrome without cystinuria (
770754006) -
2q33.1 microdeletion syndrome (
763062006) -
3-methylglutaconic aciduria type 9 (
1222672002) -
4q25 proximal deletion syndrome (
1251452003) -
5-amino-4-imidazole carboxamide ribosiduria (
725289009) -
5p13 microduplication syndrome (
770793002) -
8q24.3 microdeletion syndrome (
1229895008) -
9q21.13 microdeletion syndrome (
1229875002) -
9q31.1q31.3 microdeletion syndrome (
773493002) -
9q33.3q34.11 microdeletion syndrome (
1228886008) -
AT-hook DNA binding motif containing 1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome (
774068004) -
Ability to recognize faces (
285165006) -
Ability to recognize faces by sight (
285167003) -
Ability to recognize familiar people (
285772002) -
Ability to recognize objects (
225667008) -
Ability to recognize objects by sight (
285162009) -
Ability to recognize objects by touch (
285158003) -
Ability to recognize odors (
285184009) -
Ability to recognize other persons (
225432002) -
Ability to recognize own fingers (
285789005) -
Ability to recognize parts of own body (
285778003) -
Ability to recognize self (
225433007) -
Ability to recognize social cues (
1187234002) -
Ability to recognize sounds (
285172007) -
Ability to recognize surroundings (
285175009) -
Ability to recognize symptoms (
700485008) -
Ability to recognize warning sounds (
285181001) -
Able to recognize faces (
285170004) -
Able to recognize faces by sight (
285168008) -
Able to recognize familiar people (
285773007) -
Able to recognize objects (
285156004) -
Able to recognize objects by sight (
285163004) -
Able to recognize objects by touch (
285159006) -
Able to recognize odors (
285185005) -
Able to recognize own emotional pain and distress (
716439008) -
Able to recognize own fingers (
285790001) -
Able to recognize pain in body part (
716440005) -
Able to recognize parts of own body (
285779006) -
Able to recognize sounds (
285173002) -
Able to recognize surroundings (
285176005) -
Able to recognize warning sounds (
285182008) -
Achalasia microcephaly syndrome (
718573009) -
Acquired language comprehension impairment (
716306006) -
Activity dependent neuroprotector homeobox related multiple congenital anomalies, intellectual disability, autism spectrum disorder (
766824003) -
Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome (
722281001) -
Age-related cognitive decline (
102891000) -
Agenesis of corpus callosum and abnormal genitalia syndrome (
763797003) -
Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome (
722282008) -
Agenesis of corpus callosum, macrocephaly, hypertelorism syndrome (
1208720000) -
Akinetic-rigid form of Huntington's disease (
230301006) -
Alaninuria, microcephaly, dwarfism, enamel hypoplasia, diabetes mellitus syndrome (
733072002) -
Aldehyde dehydrogenase 18 family member A1-related de Barsy syndrome (
1295485009) -
Alopecia and intellectual disability syndrome (
716191002) -
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (
720981000) -
Alopecia, contracture, dwarfism, intellectual disability syndrome (
720979002) -
Alopecia, epilepsy, intellectual disability syndrome Moynahan type (
788417006) -
Alopecia, progressive neurological defect, endocrinopathy syndrome (
770941005) -
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (
734349003) -
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (
720982007) -
Altered behavior due to Pick's disease (
82351000119105) -
Altered behavior in dementia due to Huntington chorea (
82361000119107) -
Alzheimer's disease (
26929004) -
Alzheimer's disease with altered behavior (
97751000119108) -
Alzheimer's disease with delirium (
142011000119109) -
Alzheimer's disease with delusions (
141991000119109) -
Alzheimer's disease with depressed mood (
142001000119106) -
Alzheimer's disease with progressive aphasia (
230280008) -
Alzheimer's disease with psychosis (
1259128002) -
Amelocerebrohypohidrotic syndrome (
109478007) -
Amnesia (
48167000) -
Amnesia for day to day facts (
247607004) -
Amnesia for important personal information (
247611005) -
Amnesia for recent events (
42176003) -
Amnesia for remote events (
6149008) -
Amnestic mild cognitive disorder (
836301008) -
Amorphosynthesis (
90406001) -
Amyotrophic lateral sclerosis with frontotemporal dementia (
1259124000) -
Amyotrophic lateral sclerosis, parkinsonism, dementia complex (
838276009) -
Amyotrophic lateral sclerosis, parkinsonism, dementia complex of Kii Peninsula (
1259123006) -
Amyotrophic lateral sclerosis, parkinsonism, dementia complex of West New Guinea (
1259121008) -
Angelman syndrome (
76880004) -
Angelman syndrome due to maternal monosomy 15q11q13 (
1162462009) -
Aniridia and intellectual disability syndrome (
720468000) -
Aniridia, renal agenesis, psychomotor retardation syndrome (
733116005) -
Ankyrin 3 related intellectual disability, sleep disturbance syndrome (
787175002) -
Anterior maxillary protrusion, strabismus, intellectual disability syndrome (
1222706005) -
Anterograde amnesia (
88822006) -
Antigen recognition site (
62504002) -
Anxiety about altered body image (
225644006) -
Anxiety about appearing ridiculous (
277838008) -
Anxiety about becoming fat (
277831002) -
Anxiety about behavior or performance (
247825008) -
Anxiety about blushing (
89225005) -
Anxiety about body function or health (
247808006) -
Anxiety about breathlessness (
702535006) -
Anxiety about choking (
277822002) -
Anxiety about collapsing (
277824001) -
Anxiety about dying (
277827008) -
Anxiety about fainting (
277833004) -
Anxiety about forced dependence (
225636006) -
Anxiety about going crazy (
277828003) -
Anxiety about having a fit (
277821009) -
Anxiety about having a heart attack (
277834005) -
Anxiety about lethargy (
323341000000102) -
Anxiety about losing control of bowels (
277818007) -
Anxiety about losing emotional control (
277829006) -
Anxiety about loss of control (
225637002) -
Anxiety about loss of memory (
431432003) -
Anxiety about making mistakes (
225643000) -
Anxiety about mood (
323351000000104) -
Anxiety about not coping with parenthood (
225642005) -
Anxiety about resuming sexual relations (
225638007) -
Anxiety about saying the wrong thing (
277839000) -
Anxiety about shaking (
277825000) -
Anxiety about swallowing (
277823007) -
Anxiety about sweating (
277826004) -
Anxiety about treatment (
225635005) -
Anxiety about visiting dentist (
1255960000) -
Anxiety about vomiting in public (
277820005) -
Anxiety about wetting self (
277819004) -
Anxious cognitions (
139598003) -
Anxious cognitions (
247649009) -
Aortic arch anomaly, facial dysmorphism, intellectual disability syndrome (
763615003) -
Aphonia, deafness, retinal dystrophy, bifid halluces, intellectual disability syndrome (
773583007) -
Aplastic anemia, intellectual disability, dwarfism syndrome (
1332385000) -
Arachnodactyly and intellectual disability with facial dysmorphism syndrome (
720502000) -
Arachnodactyly with abnormal ossification and intellectual disability syndrome (
720501007) -
Arginine-glutamic acid dipeptide repeats-related neurodevelopmental syndrome (
1172624000) -
Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy (
1220600004) -
Arrhythmia-recognition training model (
463030000) -
Arteriosclerotic dementia with delirium (
191464005) -
Arteriosclerotic dementia with depression (
191466007) -
Arteriosclerotic dementia with paranoia (
191465006) -
Assessment using Birmingham Object Recognition Battery (
716216000) -
Assessment using Birmingham Object Recognition Battery (
967501000000104) -
Assessment using Everyday Cognition questionnaire (
714328009) -
Assessment using Everyday Cognition questionnaire (
935391000000103) -
Assessment using General Practitioner assessment of Cognition (
763296008) -
Assessment using General Practitioner assessment of Cognition (
1085381000000104) -
Assessment using Posttraumatic Cognitions Inventory (
3000341000000109) -
Ataxia with deafness and intellectual disability syndrome (
720517001) -
Ataxia, photosensitivity, short stature syndrome (
773769008) -
Atypical hypotonia cystinuria syndrome (
778025006) -
Aural atresia with multiple congenital anomalies and intellectual disability syndrome (
720748007) -
Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency (
771448004) -
Autism spectrum disorder due to AUTS2 activator of transcription and developmental regulator deficiency (
771512003) -
Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein (
1156789004) -
Autosomal dominant Alzheimer disease due to mutation of presenilin 1 (
1156800008) -
Autosomal dominant Alzheimer disease due to mutation of presenilin 2 (
1156798001) -
Autosomal dominant deafness with onychodystrophy syndrome (
1208614008) -
Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome (
1255319004) -
Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1.4 linker histone, cluster member mutation (
1304277005) -
Autosomal recessive cerebellar ataxia due to CWF19 like cell cycle control factor 1 deficiency (
1237625002) -
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency (
773498006) -
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency (
770898002) -
Autosomal recessive chorioretinopathy and microcephaly syndrome (
770404004) -
Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction (
1186734006) -
Autosomal recessive intellectual disability, motor dysfunction, multiple joint contracture syndrome (
770901001) -
Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome (
771476007) -
Baraitser Winter cerebrofrontofacial syndrome (
1258972007) -
Bardet-Biedl syndrome (
5619004) -
Basel Vanagaite Smirin Yosef syndrome (
1187644009) -
Behavioral disturbance due to multi-infarct dementia (
293671000119109) -
Behavioral variant of frontotemporal dementia (
716994006) -
Biemond syndrome type 2 (
717887003) -
Birmingham Object Recognition Battery score (
973601000000103) -
Birmingham Object Recognition Battery score (
716606004) -
Birmingham object recognition battery (
273321002) -
Blepharonasofacial malformation syndrome (
717913006) -
Blepharophimosis, intellectual disability syndrome (
788584007) -
Blepharophimosis, intellectual disability syndrome, Say-Barber-Biesecker-Young-Simpson type (
699298009) -
Blepharophimosis, intellectual disability syndrome, Verloes type (
778009001) -
Blepharophimosis, intellectual disability syndrome/genitopatellar overlap syndrome (
1304113005) -
Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type (
699297004) -
Borderline cognitive developmental delay (
18541000119100) -
Borderline intellectual disability (
77287004) -
Borjeson-Forssman-Lehmann syndrome (
21634003) -
Brachydactyly and preaxial hallux varus syndrome (
732957009) -
Brachydactyly, mesomelia, intellectual disability, heart defect syndrome (
765761009) -
Brachymorphism with onychodysplasia and dysphalangism syndrome (
720573009) -
Brain anomaly, severe intellectual disability, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome (
717945001) -
Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome (
1169355000) -
Branchial dysplasia, intellectual disability, inguinal hernia syndrome (
732961003) -
Branchioskeletogenital syndrome (
719097002) -
Bullous dystrophy macular type (
725589005) -
CK syndrome (
773329005) -
Calcium/calmodulin-dependent serine protein kinase related intellectual disability (
703389002) -
Carboxypeptidase E-related Prader-Willi-like syndrome (
1340175001) -
Caudal appendage deafness syndrome (
726621009) -
Central nervous system calcification, deafness, tubular acidosis, anemia syndrome (
726669007) -
Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome (
763344007) -
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (
726031001) -
Cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anemia, growth retardation syndrome (
1332508004) -
Cerebro-facio-thoracic dysplasia (
720635002) -
Cerebrofacioarticular syndrome (
763353000) -
Cerebrooculonasal syndrome (
720855003) -
Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome (
763136000) -
Cherubism with gingival fibromatosis (
389273002) -
Chloride voltage-gated channel 4-related X-linked intellectual disability syndrome (
1172691004) -
Chromodomain helicase DNA binding protein 4-related neurodevelopmental disorder (
1332510002) -
Chromodomain helicase dna-binding protein 3- related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome (
1179408008) -
Chromosome 11p11.2 deletion syndrome (
702346005) -
Chromosome Xp11.3 microdeletion syndrome (
719808002) -
Chronic traumatic encephalopathy (
1187004001) -
City Birth Trauma Scale negative cognitions and mood symptoms score (
1658981000000107) -
Clark Baraitser syndrome (
1300132009) -
Cleft palate with short stature and vertebral anomaly syndrome (
719466009) -
Cleft palate, congenital heart defect, intellectual disability syndrome (
1335869007) -
Coffin-Lowry syndrome (
15182000) -
Coffin-Siris syndrome (
10007009) -
Cognition Therapy Outcome Measure activity score (
1062771000000106) -
Cognition Therapy Outcome Measure carer wellbeing score (
1062781000000108) -
Cognition Therapy Outcome Measure impairment score (
1062791000000105) -
Cognition Therapy Outcome Measure participation score (
1062801000000109) -
Cognition Therapy Outcome Measure wellbeing score (
1062811000000106) -
Cognition finding simple reference set (
999001481000000105) -
Cognitions questionnaire (
273374007) -
Cognitive changes due to organic disorder (
141601000119107) -
Cognitive communication disorder (
716635007) -
Cognitive deficit due to and following cerebrovascular disease (
290621000119101) -
Cognitive deficit due to and following embolic cerebrovascular accident (
690341000119100) -
Cognitive deficit due to and following hemorrhagic cerebrovascular accident (
672571000119109) -
Cognitive deficit due to and following ischemic cerebrovascular accident (
672561000119103) -
Cognitive deficit due to and following nontraumatic intracerebral hemorrhage (
291711000119109) -
Cognitive deficit due to and following nontraumatic subarachnoid hemorrhage (
291621000119109) -
Cognitive deficit in attention (
142261000119100) -
Cognitive deficit in psychomotor function (
142291000119107) -
Cognitive deficit in visuospatial function (
142281000119109) -
Cognitive developmental delay (
425805004) -
Cognitive disorder (
443265004) -
Cognitive disorder in remission (
698691002) -
Cognitive dysfunction following surgical procedure (
771417007) -
Cognitive impairment caused by ethanol (
1234774002) -
Cognitive impairment co-occurrent and due to human immunodeficiency virus infection (
15928141000119107) -
Cognitive impairment co-occurrent and due to primary psychotic disorder (
724760003) -
Cognitive impairment due to late-delayed irradiation of brain (
1259562009) -
Cognitive impairment due to lead toxicity (
1186839009) -
Cognitive impairment due to toxicity of substance (
762298000) -
Cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, skeletal dysplasia syndrome (
764455002) -
Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome (
720639008) -
Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome (
776204008) -
Combined oxidative phosphorylation defect type 23 (
1173036000) -
Combined oxidative phosphorylation defect type 39 (
1279845005) -
Congenital cataract with ataxia and deafness syndrome (
719102004) -
Congenital cataract with deafness and hypogonadism syndrome (
722378009) -
Congenital cataract with hypertrichosis and intellectual disability syndrome (
722379001) -
Congenital cataract with intellectual disability and anal atresia and urinary defect syndrome (
715989002) -
Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome (
722380003) -
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (
1177169004) -
Congenital contracture of limbs and face, hypotonia, developmental delay syndrome (
1255322002) -
Congenital hypoplasia of ulna and intellectual disability syndrome (
719842006) -
Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome (
1208936008) -
Congenital insensitivity to pain with severe intellectual disability (
1237623009) -
Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome (
1172594000) -
Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome (
782757004) -
Congenital muscular dystrophy with intellectual disability (
783174004) -
Congenital muscular dystrophy with intellectual disability and severe epilepsy (
782772000) -
Congenital pontocerebellar hypoplasia type 11 (
1300188000) -
Congenital pontocerebellar hypoplasia type 14 (
1300192007) -
Contactin associated protein 2-related developmental and epileptic encephalopathy (
1230376005) -
Contracture with ectodermal dysplasia and orofacial cleft syndrome (
720746006) -
Cortical blindness, intellectual disability, polydactyly syndrome (
732251003) -
Cortical vascular dementia (
833326008) -
Craniodigital syndrome and intellectual disability syndrome (
763665007) -
Craniofacial digital and genital anomalies syndrome (
716089008) -
Craniofacial dysmorphism with coloboma of eye and corpus callosum agenesis syndrome (
719947004) -
Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome (
1217229007) -
Craniofaciofrontodigital syndrome (
763320005) -
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (
1269224009) -
Cross syndrome (
17827007) -
Cryptorchidism, arachnodactyly, intellectual disability syndrome (
764950001) -
Cyclin K-related neurodevelopmental disorder, severe intellectual disability, facial dysmorphism syndrome (
1332384001) -
Cyclin dependent kinase 13-related congenital heart defects, intellectual disability, facial dysmorphism syndrome (
1299154002) -
Cyclin-dependent kinase-like 5 developmental and epileptic encephalopathy (
773230003) -
Cystic fibrosis with gastritis and megaloblastic anemia syndrome (
720401009) -
Cystic leukoencephalopathy without megalencephaly (
720825005) -
Deafness and intellectual disability Martin Probst type syndrome (
721087008) -
Deafness with onychodystrophy syndrome (
773735007) -
Deafness with skeletal dysplasia and lip granuloma syndrome (
720957007) -
Deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome (
721086004) -
Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (
719800009) -
Deafness-dystonia-optic neuronopathy syndrome (
702423009) -
Delirium co-occurrent with dementia (
725898002) -
Dementia (
52448006) -
Dementia associated with Parkinson's Disease (
425390006) -
Dementia associated with alcoholism (
281004) -
Dementia associated with another disease (
191519005) -
Dementia associated with cerebral anoxia (
698781002) -
Dementia associated with cerebral lipidosis (
698624003) -
Dementia associated with multiple sclerosis (
698626001) -
Dementia associated with neurosyphilis (
698725008) -
Dementia associated with normal pressure hydrocephalus (
698625002) -
Dementia associated with viral encephalitis (
698726009) -
Dementia caused by drug (
191493005) -
Dementia caused by heavy metal exposure (
733184002) -
Dementia caused by ionizing radiation (
1339031006) -
Dementia caused by manganese and/or manganese compound (
1186887004) -
Dementia caused by volatile inhalant (
788898005) -
Dementia co-occurrent and due to Down syndrome (
733194007) -
Dementia co-occurrent and due to Pick's disease (
21921000119103) -
Dementia co-occurrent and due to neurocysticercosis (
722977005) -
Dementia co-occurrent and due to progressive multifocal leukoencephalopathy (
733193001) -
Dementia co-occurrent with human immunodeficiency virus infection (
713844000) -
Dementia due to Behcet syndrome (
1259579003) -
Dementia due to Creutzfeldt Jakob disease (
429458009) -
Dementia due to Gerstmann Straussler Scheinker syndrome (
1259469003) -
Dementia due to Hashimoto encephalopathy (
1259471003) -
Dementia due to Huntington chorea (
442344002) -
Dementia due to Lewy body disease (
1363185006) -
Dementia due to Lyme disease (
1259496000) -
Dementia due to Parkinson's disease (
101421000119107) -
Dementia due to Rett syndrome (
130121000119104) -
Dementia due to Whipple disease (
1259513009) -
Dementia due to Wilson disease (
1259511006) -
Dementia due to acquired hypothyroidism (
1259591007) -
Dementia due to and following dialysis (
1259584009) -
Dementia due to and following injury of head (
762351006) -
Dementia due to atypical pantothenate kinase associated neurodegeneration (
1259679007) -
Dementia due to autoimmune encephalitis (
1259586006) -
Dementia due to carbon monoxide poisoning (
840464007) -
Dementia due to celiac disease (
1259581001) -
Dementia due to cerebral amyloid angiopathy (
1259488005) -
Dementia due to cerebral vasculitis (
1259485008) -
Dementia due to chromosomal anomaly (
722980006) -
Dementia due to chronic intracranial subdural hematoma (
733191004) -
Dementia due to classical pantothenate kinase associated neurodegeneration (
1259990004) -
Dementia due to cobalamin deficiency (
1186880002) -
Dementia due to deficiency of folic acid (
1148924004) -
Dementia due to disorder of central nervous system (
724776007) -
Dementia due to familial Creutzfeldt-Jakob disease (
1259478009) -
Dementia due to fatal familial insomnia (
1259480003) -
Dementia due to fragile X syndrome (
1259473000) -
Dementia due to genetic disease (
1259476008) -
Dementia due to hemorrhagic cerebral infarction due to hypertension (
1259499007) -
Dementia due to hepatic failure (
1259465009) -
Dementia due to herpes encephalitis (
733192006) -
Dementia due to hypercalcemia (
1259467001) -
Dementia due to hypertensive encephalopathy (
1259531005) -
Dementia due to iatrogenic Creutzfeldt-Jakob disease (
1259503001) -
Dementia due to infectious disease (
724777003) -
Dementia due to inflammatory disorder of musculoskeletal system (
1259661008) -
Dementia due to iron deficiency (
840465008) -
Dementia due to kuru (
1259501004) -
Dementia due to leukodystrophy (
1259494002) -
Dementia due to metabolic abnormality (
722979008) -
Dementia due to metastatic malignant neoplasm to brain (
1259492003) -
Dementia due to multiple sclerosis with altered behavior (
82371000119101) -
Dementia due to multiple system atrophy (
1259677009) -
Dementia due to neurofilament inclusion body disease (
1259673008) -
Dementia due to niacin deficiency (
1186881003) -
Dementia due to nutritional deficiency disorder (
1186883000) -
Dementia due to obstructive hydrocephalus (
1259675001) -
Dementia due to paraneoplastic encephalitis (
1259667007) -
Dementia due to pellagra (
788899002) -
Dementia due to polyarteritis nodosa (
1259663006) -
Dementia due to primary malignant neoplasm of brain (
733190003) -
Dementia due to prion disease (
762350007) -
Dementia due to progressive subcortical gliosis (
1259665004) -
Dementia due to renal failure (
1259656006) -
Dementia due to sporadic Creutzfeldt-Jakob disease (
1259529001) -
Dementia due to subacute sclerosing panencephalitis (
1259519008) -
Dementia due to systemic lupus erythematosus (
1259517005) -
Dementia due to thiamine deficiency (
1186879000) -
Dementia due to trypanosomiasis (
1259524006) -
Dementia due to variant Creutzfeldt-Jakob disease (
1259522005) -
Dementia due to vitamin E deficiency (
1186877003) -
Dementia in remission (
698949001) -
Dementia of frontal lobe type (
278857002) -
Dementia of the Alzheimer type with behavioral disturbance (
1581000119101) -
Dementia paralytica juvenilis (
82959004) -
Dementia with acquired immunodeficiency syndrome (
421529006) -
Dementia with behavioral disturbance (
1591000119103) -
Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome (
721089006) -
Developmental and speech delay due to SRY-box 5 deficiency (
771472009) -
Developmental delay with autism spectrum disorder and gait instability (
770790004) -
Developmental delay, facial dysmorphism syndrome due to mediator complex subunit 13 like deficiency (
787093004) -
Developmental delay, language impairment, dopa responsive dystonia, parkinsonism syndrome (
1380254000) -
Diabetes, hypogonadism, deafness, intellectual disability syndrome (
816067005) -
Dialysis dementia (
9345005) -
Dibasic amino aciduria type 1 (
50056009) -
Diencephalic mesencephalic junction dysplasia (
766871009) -
Difficulty recognising familiar people (
1068921000000107) -
Difficulty recognising generalised pain (
1070721000000101) -
Difficulty recognising need for pressure area care (
1068931000000109) -
Difficulty recognising objects (
1070761000000109) -
Difficulty recognising objects by sight (
1070771000000102) -
Difficulty recognising objects by touch (
1070781000000100) -
Difficulty recognising own emotional pain and distress (
1070791000000103) -
Difficulty recognising own symptoms (
1070681000000108) -
Difficulty recognising pain in body part (
1068941000000100) -
Difficulty recognising surroundings (
1070801000000104) -
Digit span forwards performance impaired (
1386319000) -
Digit span reverse performance impaired (
1386320006) -
Disinhibited behavior due to dementia (
789170003) -
Disorder of sex development with intellectual disability syndrome (
719450007) -
Dissociative amnesia (
84209002) -
Dissociative neurological symptom disorder co-occurrent with cognitive impairment (
736314008) -
Disturbance of cognitive learning (
116340000) -
Disturbance of memory for order of events (
416106008) -
Does not recognise familiar people (
1072411000000103) -
Does not recognise generalised pain (
1072421000000109) -
Does not recognise need for pressure area care (
1072441000000102) -
Does not recognise objects (
1072451000000104) -
Does not recognise objects by sight (
1072461000000101) -
Does not recognise objects by touch (
1069171000000103) -
Does not recognise own emotional pain and distress (
1072471000000108) -
Does not recognise own symptoms (
1072371000000102) -
Does not recognise pain in body part (
1072481000000105) -
Does not recognise surroundings (
1072491000000107) -
Does not recognize photographs of self (
225664001) -
Does not recognize self (
225434001) -
Does not recognize self in mirror (
225435000) -
Does recognise familiar people (
1069401000000103) -
Does recognise generalised pain (
1074061000000104) -
Does recognise need for pressure area care (
1069411000000101) -
Does recognise objects (
1074101000000102) -
Does recognise objects by sight (
1074111000000100) -
Does recognise objects by touch (
1069421000000107) -
Does recognise own emotional pain and distress (
1074121000000106) -
Does recognise own symptoms (
1074021000000107) -
Does recognise pain in body part (
1074131000000108) -
Does recognise surroundings (
1074141000000104) -
Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome (
1179301003) -
Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion (
783619003) -
Dysequilibrium syndrome (
230782004) -
Dysmorphism, short stature, deafness, disorder of sex development syndrome (
733050004) -
Early onset Alzheimer's disease with behavioral disturbance (
105421000119105) -
Early onset dementia due to Lewy body disease (
1363184005) -
Early onset parkinsonism and intellectual disability syndrome (
716107009) -
Early-onset epilepsy, intellectual disability, brain anomalies syndrome (
1172627007) -
Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome (
773548008) -
Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome (
1187042007) -
Ectodermal dysplasia with blindness syndrome (
721208007) -
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (
734017008) -
Education about impaired cognition (
1153468002) -
Education of family about impaired cognition (
1153467007) -
Encephalopathy due to mitochondrial and peroxisomal fission defect (
1236807002) -
Encephalopathy, intracerebral calcification, retinal degeneration syndrome (
733049004) -
Epidermal growth factor-related primary hypomagnesemia with intellectual disability (
1351962002) -
Epilepsy co-occurrent and due to dementia (
724992007) -
Epilepsy telangiectasia syndrome (
733032006) -
Epilepsy, microcephaly, skeletal dysplasia syndrome (
733031004) -
Epileptic dementia with behavioral disturbance (
82381000119103) -
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (
766870005) -
Erythrophobia (
1343608003) -
Everyday Cognition questionnaire (
934131000000103) -
Everyday Cognition questionnaire (
714284006) -
Everyday Cognition questionnaire (
934141000000107) -
Everyday Cognition questionnaire completed (
934111000000106) -
Everyday Cognition questionnaire completed (
934121000000100) -
Everyday Cognition questionnaire score (
935401000000100) -
Everyday Cognition questionnaire score (
714338004) -
Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome (
771179007) -
FG syndrome type 1 (
1237179007) -
FRAXE intellectual disability syndrome (
716709002) -
Facial dysmorphism, cleft palate, loose skin syndrome (
763278004) -
Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion (
783061008) -
Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome (
733417008) -
Facial recognition test (
273450008) -
Faciocardiorenal syndrome (
723333000) -
Fallot complex with intellectual disability and growth delay syndrome (
723336008) -
False recognition (
85173004) -
Familial Alzheimer's disease of early onset (
230265002) -
Familial Alzheimer's disease of late onset (
230267005) -
Familial dementia British type (
783161005) -
Familial dementia Danish type (
783258000) -
Familial multiple system deposition of tau protein (
1260328002) -
Fatal X-linked ataxia with deafness and loss of vision (
702441001) -
Fatty acyl-coenzyme A reductase 1 deficiency (
1237619001) -
Feels at risk of crime in neighborhood (
413301003) -
Feels unsafe around family (
1471821000168101) -
Feels unsafe around friends (
1471831000168103) -
Feels unsafe at home (
1471791000168109) -
Feels unsafe in neighborhood (
1471781000168106) -
Fibulin 1-related developmental delay, central nervous system anomaly, syndactyly syndrome (
774070008) -
Filippi syndrome (
720954000) -
Finding related to ability to recognize faces (
365606002) -
Finding related to ability to recognize faces by sight (
365617001) -
Finding related to ability to recognize familiar people (
365628002) -
Finding related to ability to recognize objects (
365518001) -
Finding related to ability to recognize objects by sight (
365540005) -
Finding related to ability to recognize objects by touch (
365529002) -
Finding related to ability to recognize odors (
365572008) -
Finding related to ability to recognize other persons (
365594000) -
Finding related to ability to recognize own fingers (
365661009) -
Finding related to ability to recognize parts of own body (
365650001) -
Finding related to ability to recognize self (
365639004) -
Finding related to ability to recognize sounds (
365551005) -
Finding related to ability to recognize surroundings (
365583004) -
Finding related to ability to recognize warning sounds (
365562005) -
Finding related to recognition (
225431009) -
Fine Lubinsky syndrome (
720955004) -
Focal Alzheimer's disease (
230269008) -
Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome (
765089003) -
Forgetful (
55533009) -
Forgets to take medication (
1303576005) -
Fragile X syndrome (
613003) -
Fried syndrome (
718848000) -
Frontal lobe degeneration with motor neurone disease (
230274000) -
Frontal variant non-amnestic Alzheimer disease (
1263585001) -
Frontotemporal dementia (
230270009) -
Frontotemporal dementia due to C9orf72 mutation (
1260354005) -
Frontotemporal dementia due to FUS mutation (
1260355006) -
Frontotemporal dementia due to TARDBP mutation (
1260352009) -
Frontotemporal dementia due to VCP mutation (
1260353004) -
Frontotemporal dementia with gene located on 3p11 (
702393003) -
Frontotemporal dementia with parkinsonism-17 (
702429008) -
Fryns Smeets Thiry syndrome (
1208344000) -
G protein subunit beta 5-related intellectual disability, cardiac arrhythmia syndrome (
1186711002) -
GPCOG - general practitioner assessment of cognition informant score (
754251000000108) -
GPCOG - general practitioner assessment of cognition patient score (
754231000000101) -
GRN-related frontotemporal dementia (
702426001) -
Gabriele-de Vries syndrome (
1186730002) -
General Practitioner Assessment of Cognition (
770753000) -
General paresis - neurosyphilis (
51928006) -
General practitioner assessment of cognition informant interview (
754241000000105) -
General practitioner assessment of cognition informant score (
756501000000101) -
General practitioner assessment of cognition patient examination (
754221000000103) -
General practitioner assessment of cognition patient score (
756511000000104) -
General practitioner assessment of cognition score (
756521000000105) -
General practitioner assessment of cognition tool (
504121000000102) -
General practitioner assessment of cognition tool (
757751000000108) -
Genetic intellectual disability (
1362108000) -
Gillespie syndrome (
253176002) -
Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome (
1222658006) -
Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome (
1172630000) -
Glutamate ionotropic receptor NMDA type subunit 2B-related developmental delay, intellectual disability, autism spectrum disorder (
1260195002) -
Glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A developmental and epileptic encephalopathy (
770431001) -
Glutamine rich 1-related intellectual disability, chondrodysplasia syndrome (
1220568003) -
Goldberg Shprintzen megacolon syndrome (
717822006) -
Goniodysgenesis with intellectual disability and short stature syndrome (
716024001) -
Growth delay, intellectual disability, hepatopathy syndrome (
1186713004) -
Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (
721843003) -
Grubben, De Cock, Borghgraef syndrome (
763186006) -
Hair defect with photosensitivity and intellectual disability syndrome (
721007005) -
Hall Riggs syndrome (
721008000) -
Hallucinations co-occurrent and due to late onset dementia (
2421000119107) -
Hao Fountain syndrome (
1360075006) -
Hao Fountain syndrome due to 16p13.2 microdeletion (
1228890005) -
Hennekam lymphangiectasia-lymphedema syndrome (
234146006) -
Hepatic fibrosis, renal cyst, intellectual disability syndrome (
771149000) -
Hereditary cryohydrocytosis with reduced stomatin (
782911008) -
Hereditary persistence of fetal hemoglobin, intellectual disability syndrome (
1360079000) -
HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (
1186724002) -
Human immunodeficiency virus type I enhancer binding protein 2 related intellectual disability (
765434008) -
Huntington's chorea (
58756001) -
Hyperekplexia epilepsy syndrome (
785726009) -
Hyperphosphatasemia with intellectual disability (
33982008) -
Hypogonadism with mitral valve prolapse and intellectual disability syndrome (
721841001) -
Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome (
773553003) -
Hypoplasia of corpus callosum, intellectual disability, adducted thumbs, spasticity, hydrocephalus syndrome (
716996008) -
Hypospadias and intellectual disability syndrome Goldblatt type (
716096005) -
Hypotonia, speech impairment, severe cognitive delay syndrome (
763722004) -
Hypotrichosis and intellectual disability syndrome Lopes type (
723365002) -
Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome (
763404001) -
Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome (
733097003) -
Impaired cognition (
80216008) -
Impaired cognition (
386806002) -
Impaired cognition (
918271000000105) -
Impaired concentration (
1144748009) -
Impaired environmental interpretation syndrome (
130964008) -
Impaired executive functioning (
736317001) -
Impairment of registration (
283878007) -
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly (
770725000) -
Infantile choroidocerebral calcification syndrome (
724228005) -
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome (
1217371005) -
Infantile inflammatory bowel disease with neurological involvement (
1186721005) -
Infantile multisystem neurologic, endocrine, pancreatic disease (
1260450002) -
Infantile neurodegeneration, progressive spasticity, intellectual disability, white matter lesions syndrome (
1303585005) -
Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome (
782886007) -
Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome (
1260129000) -
Information conversion problem (
76789006) -
Inhalant-induced persisting dementia (
32875003) -
Integral membrane protein 2B related amyloidosis (
1187126002) -
Intellectual development disorder with impairment of behaviour (
1094031000000100) -
Intellectual development disorder with minimal impairment of behaviour (
1094021000000102) -
Intellectual development disorder with significant impairment of behaviour (
1094011000000108) -
Intellectual development disorder without significant impairment of behaviour (
1094001000000106) -
Intellectual disability (
110359009) -
Intellectual disability Birk-Barel type (
764861005) -
Intellectual disability Buenos Aires type (
725906006) -
Intellectual disability Wolff type (
763745005) -
Intellectual disability and short stature with hand contracture and genital anomaly syndrome (
716334004) -
Intellectual disability due to nutritional deficiency (
763626009) -
Intellectual disability with strabismus syndrome (
773405004) -
Intellectual disability, alacrima, achalasia syndrome (
763741001) -
Intellectual disability, aphasia, shuffling gait, adducted thumbs syndrome (
838441009) -
Intellectual disability, autism, speech apraxia, craniofacial dysmorphism syndrome (
1217382002) -
Intellectual disability, balding, patella luxation, acromicria syndrome (
722002002) -
Intellectual disability, brachydactyly, Pierre Robin syndrome (
763744009) -
Intellectual disability, cardiac anomalies, short stature, joint laxity syndrome (
1186729007) -
Intellectual disability, cataract, calcified pinna, myopathy syndrome (
726709001) -
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome (
782753000) -
Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth (
412787009) -
Intellectual disability, craniofacial dysmorphism, cryptorchidism syndrome (
773581009) -
Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome (
722454003) -
Intellectual disability, cupped ears syndrome (
1351837003) -
Intellectual disability, developmental delay, contracture syndrome (
722456001) -
Intellectual disability, early-onset cataract, microcephaly syndrome (
1351838008) -
Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome (
722035007) -
Intellectual disability, epilepsy, bulbous nose syndrome (
721146009) -
Intellectual disability, epilepsy, extrapyramidal syndrome (
1187210007) -
Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome (
722037004) -
Intellectual disability, expressive aphasia, facial dysmorphism syndrome (
1197593006) -
Intellectual disability, facial dysmorphism syndrome due to SET domain containing 5 haploinsufficiency (
782736007) -
Intellectual disability, facial dysmorphism, hand anomalies syndrome (
773416006) -
Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome (
773552008) -
Intellectual disability, hyperkinetic movement, truncal ataxia syndrome (
787174003) -
Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome (
722455002) -
Intellectual disability, hypotonia, brachycephaly, pyloric stenosis, cryptorchidism syndrome (
773621003) -
Intellectual disability, macrocephaly, hypotonia, behavioral abnormalities syndrome (
1254652005) -
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome (
1208746001) -
Intellectual disability, myopathy, short stature, endocrine defect syndrome (
764959000) -
Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome (
763350002) -
Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome (
774102003) -
Intellectual disability, polydactyly, uncombable hair syndrome (
763742008) -
Intellectual disability, seizures, abnormal gait, facial dysmorphism syndrome (
1177167002) -
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome (
770755007) -
Intellectual disability, seizures, macrocephaly, obesity syndrome (
770750002) -
Intellectual disability, severe speech delay, mild dysmorphism syndrome (
774203000) -
Intellectual disability, short stature, hypertelorism syndrome (
771077007) -
Intellectual disability, spasticity, ectrodactyly syndrome (
763743003) -
Intellectual disability, speech delay, dysmorphic features, T cell abnormalities syndrome (
1373748007) -
Intellectual disability, truncal obesity, retinal dystrophy and micropenis syndrome (
715628009) -
Ischemic vascular dementia (
723123001) -
Isodicentric chromosome 15 syndrome (
723332005) -
Jawad syndrome (
771470001) -
Juberg Marsidi syndrome (
721875000) -
Juvenile onset Huntington's disease (
230299004) -
Kagami Ogata syndrome (
770907002) -
Kapur Toriello syndrome (
722031003) -
Keppen Lubinsky syndrome (
1220589007) -
Kleefstra syndrome (
724207001) -
Lack of thinking ability (
110355003) -
Lamb Shaffer syndrome (
1251453008) -
Language-related cognitive disorder (
229676007) -
Laryngeal abductor paralysis with intellectual disability syndrome (
724178000) -
Late onset Alzheimer's dementia with behavioral disturbance (
16219201000119101) -
Late onset Huntington's disease (
230300007) -
Late onset dementia due to Lewy body disease (
312991009) -
Late-onset localized junctional epidermolysis bullosa, intellectual disability syndrome (
773692000) -
Laurence-Moon syndrome (
232059000) -
Lewy body dementia with behavioral disturbance (
135811000119107) -
Lipodystrophy, intellectual disability, deafness syndrome (
721973006) -
Localized dissociative amnesia (
225040001) -
Logopenic non-amnestic Alzheimer disease (
1263555006) -
Lowe syndrome (
79385002) -
Lowry MacLean syndrome (
721974000) -
Lysine demethylase 3B-related intellectual disability, facial dysmorphism, short stature syndrome (
1351843001) -
Macrocephaly and developmental delay syndrome (
763773007) -
Macrocephaly, intellectual disability, autism syndrome (
783089006) -
Macrocephaly, intellectual disability, left ventricular non compaction syndrome (
1187642008) -
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome (
1187304005) -
Macrocephaly, obesity, mental disability, ocular abnormality syndrome (
724137002) -
Macrocephaly, short stature, paraplegia syndrome (
722033000) -
Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome (
1172685001) -
Malan overgrowth syndrome (
763795006) -
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (
722459008) -
Marfanoid habitus with autosomal recessive intellectual disability syndrome (
733062000) -
McDonough syndrome (
715441004) -
Megaconial congenital muscular dystrophy (
1230273004) -
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome (
1260143005) -
Megalocornea with intellectual disability syndrome (
733522005) -
Memory deficit due to and following cerebrovascular accident (
16703661000119105) -
Memory deficit due to and following cerebrovascular disease (
16703551000119107) -
Memory deficit due to and following embolic cerebrovascular accident (
16703711000119100) -
Memory deficit due to and following hemorrhagic cerebrovascular accident (
16703821000119101) -
Memory deficit due to and following ischemic cerebrovascular accident (
16703761000119102) -
Memory deficit due to and following spontaneous intracerebral hemorrhage (
16703491000119101) -
Memory deficit due to and following spontaneous subarachnoid hemorrhage (
16703601000119109) -
Memory impairment (
386807006) -
Memory lapses (
225038006) -
Menke Hennekam syndrome (
1260095004) -
Mesomelic dysplasia, digital anomalies, intellectual disability syndrome (
1363286000) -
Metacognition, function (
312016001) -
Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome (
733419006) -
Metopic ridging, ptosis, facial dysmorphism syndrome (
1179283004) -
Microbrachycephaly, ptosis, cleft lip syndrome (
723403008) -
Microcephalic cortical malformations, short stature due to rotatin deficiency (
1187195007) -
Microcephalic primordial dwarfism Alazami type (
770564004) -
Microcephalic primordial dwarfism Dauber type (
770565003) -
Microcephalic primordial dwarfism Montreal type (
765758008) -
Microcephalus cardiomyopathy syndrome (
719380003) -
Microcephalus with brachydactyly and kyphoscoliosis syndrome (
719378009) -
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome (
764732004) -
Microcephalus, glomerulonephritis, marfanoid habitus syndrome (
733472005) -
Microcephaly with deafness and intellectual disability syndrome (
716112005) -
Microcephaly, corpus callosum and cerebellar vermis hypoplasia, facial dysmorphism, intellectual disability syndrome (
1167375003) -
Microcephaly, corpus callosum hypoplasia, intellectual disability, facial dysmorphism syndrome (
1254650002) -
Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome (
1254651003) -
Microcephaly, seizure, intellectual disability, heart disease syndrome (
723304001) -
Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome (
771074000) -
Microcephaly, thin corpus callosum, intellectual disability syndrome (
770721009) -
Micrognathia, recurrent infections, behavioral abnormalities, mild intellectual disability syndrome (
1187114007) -
Microphthalmia with ankyloblepharon and intellectual disability syndrome (
717222003) -
Microphthalmia with brain atrophy syndrome (
720010009) -
Mild intellectual development disorder with impairment of behaviour (
1093991000000101) -
Mild intellectual development disorder with minimal impairment of behaviour (
1089851000000103) -
Mild intellectual development disorder with significant impairment of behaviour (
1089841000000101) -
Mild intellectual development disorder without significant impairment of behaviour (
1089831000000105) -
Mild intellectual disability (
86765009) -
Mild memory disturbance (
192071009) -
Mild neurocognitive disorder (
386805003) -
Minimal cognitive impairment (
110352000) -
Minor memory lapses (
225037001) -
Mistakes people's identity (
225666004) -
Mixed cortical and subcortical vascular dementia (
230287006) -
Mixed dementia (
79341000119107) -
Mixes past with present (
225039003) -
Moderate cognitive impairment (
702955000) -
Moderate intellectual development disorder with impairment of behaviour (
1089821000000108) -
Moderate intellectual development disorder with minimal impairment of behaviour (
1089811000000102) -
Moderate intellectual development disorder with significant impairment of behaviour (
1089791000000103) -
Moderate intellectual development disorder without significant impairment of behaviour (
1089781000000100) -
Moderate intellectual disability (
61152003) -
Monocarboxylate transporter 8 deficiency (
702327009) -
Mowat-Wilson syndrome (
703535000) -
Mowat-Wilson syndrome due to monosomy 2q22 (
890118006) -
Multi-infarct dementia (
56267009) -
Multi-infarct dementia due to atherosclerosis (
106021000119105) -
Multi-infarct dementia with delirium (
10349009) -
Multi-infarct dementia with delusions (
25772007) -
Multi-infarct dementia with depression (
14070001) -
Multi-infarct dementia, uncomplicated (
70936005) -
Muscle eye brain disease with bilateral multicystic leukodystrophy (
785298001) -
Myelin transcription factor 1 like-related developmental delay, intellectual disability, obesity syndrome (
1303866001) -
Myhre syndrome (
699316006) -
N syndrome (
723410002) -
NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy (
1217379007) -
Neurexin 1-related severe neurodevelopmental disorder, motor stereotypies, chronic constipation, sleep-wake cycle disturbance (
1300131002) -
Neurocognitive disorder (
709073001) -
Neurodevelopmental delay, hypotonia, cerebellar ataxia, cardiac conduction defects syndrome (
1303586006) -
Neurodevelopmental delay, intellectual disability, ataxia, feeding difficulty syndrome (
1363573005) -
Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome (
1217381009) -
Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome (
1222710008) -
Neurofaciodigitorenal syndrome (
725908007) -
Neuronal ceroid lipofuscinosis type 8 (
1373770005) -
Nijmegen breakage syndrome-like disorder (
766753005) -
Non-amnestic Alzheimer disease (
722600006) -
Non-familial Alzheimer's disease of early onset (
230266001) -
Non-familial Alzheimer's disease of late onset (
230268000) -
Non-progressive cerebellar ataxia with intellectual disability (
723441001) -
Non-specific syndromic intellectual disability (
1187038009) -
Normal cognition (
449888003) -
Normal cognition (
805221000000109) -
Oculocerebrofacial syndrome Kaufman type (
722056009) -
Oculopalatocerebral syndrome (
722055008) -
Ophthalmoplegia, intellectual disability, lingua scrotalis syndrome (
782945001) -
Optic atrophy, intellectual disability syndrome (
770723007) -
Optical character recognition text document (
25841000000107) -
Organic amnesia of language (
433081000) -
Organic dementia with acquired immunodeficiency syndrome (
420614009) -
Oro-facial digital syndrome type 10 (
722075004) -
Oro-facial digital syndrome type 11 (
718681002) -
Oro-facial digital syndrome type 14 (
763837007) -
Oro-facial digital syndrome type 5 (
722105002) -
Oro-facial digital syndrome type 8 (
722106001) -
Oro-facial digital syndrome type 9 (
718680001) -
Ossification anomaly with psychomotor developmental delay syndrome (
722107005) -
Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome (
722110003) -
Osteopenia, intellectual disability, sparse hair syndrome (
732954002) -
Pachygyria, intellectual disability, epilepsy syndrome (
763861000) -
Palatal anomalies, widely spaced teeth, facial dysmorphism, developmental delay syndrome (
1172889005) -
Pallister W syndrome (
719020006) -
Paramnesia (
32541007) -
Parkinsonism co-occurrent with dementia of Guadeloupe (
715737004) -
Patchy dementia (
230289009) -
Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease (
765325002) -
Peripheral myelin protein 22-retinoic acid induced 1 contiguous gene duplication syndrome (
1172899000) -
Pervasive developmental disorder with cognitive developmental delay and complete impairment of functional language (
870308001) -
Pervasive developmental disorder with cognitive developmental delay and marked impairment of functional language (
870305003) -
Pervasive developmental disorder with disorder of intellectual development and absence of functional language with loss of previously acquired skills (
870269009) -
Pervasive developmental disorder with disorder of intellectual development and complete impairment of functional language with loss of previously acquired skills (
870270005) -
Pervasive developmental disorder with disorder of intellectual development and complete impairment of functional language without loss of previously acquired skills (
870268001) -
Pervasive developmental disorder with disorder of intellectual development and marked impairment of functional language with loss of previously acquired skills (
870266002) -
Pervasive developmental disorder with disorder of intellectual development and marked impairment of functional language without loss of previously acquired skills (
870267006) -
Pervasive developmental disorder with disorder of intellectual development and pervasive impairment of functional language without loss of previously acquired skills (
870264004) -
Pervasive developmental disorder with disorder of intellectual development with loss of previously acquired skills (
870265003) -
Pervasive developmental disorder with disorder of intellectual development without loss of previously acquired skills (
870262000) -
Phosphodiesterase 4D haploinsufficiency syndrome (
1236843008) -
Phosphoribosylpyrophosphate synthetase superactivity (
723454008) -
Pick's disease with Pick bodies (
230271008) -
Pick's disease with Pick cells and no Pick bodies (
230272001) -
Piebald trait with neurologic defects syndrome (
773984007) -
Pierpont syndrome (
1220594007) -
Pitt-Hopkins syndrome (
702344008) -
Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome (
1208987006) -
Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome (
1167371007) -
Polymicrogyria with optic nerve hypoplasia (
771336003) -
Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome (
770679002) -
Post-traumatic amnesia (
275277000) -
Post-traumatic dementia (
230282000) -
Post-traumatic dementia with behavioral change (
698687007) -
Postaxial polydactyly and intellectual disability syndrome (
721017000) -
Postconcussion syndrome (
40425004) -
Posterior-predominant lissencephaly, broad flat pons and medulla-midline crossing defects syndrome (
1269233006) -
Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome (
1173998003) -
Posttraumatic Cognitions Inventory (
3000331000000100) -
Posttraumatic Cognitions Inventory Negative Cognitions About Self score (
3000361000000105) -
Posttraumatic Cognitions Inventory Negative Cognitions About the World score (
3000371000000103) -
Posttraumatic Cognitions Inventory Self-Blame score (
3000381000000101) -
Posttraumatic Cognitions Inventory total score (
3000351000000107) -
Preaxial polydactyly, colobomata, intellectual disability syndrome (
733088002) -
Predominantly cortical dementia (
1089521000000106) -
Predominantly cortical vascular dementia (
1089531000000108) -
Presenile dementia (
12348006) -
Presenile dementia co-occurrent with human immunodeficiency virus infection (
713488003) -
Presenile dementia with acquired immunodeficiency syndrome (
421023003) -
Presenile dementia with delirium (
191452002) -
Presenile dementia with delusions (
31081000119101) -
Presenile dementia with depression (
191455000) -
Presenile dementia with paranoia (
191454001) -
Presenile dementia with psychosis (
1089501000000102) -
Primary degenerative dementia (
22381000119105) -
Primary degenerative dementia of the Alzheimer type, presenile onset (
416780008) -
Primary degenerative dementia of the Alzheimer type, presenile onset in remission (
698955006) -
Primary degenerative dementia of the Alzheimer type, presenile onset, uncomplicated (
6475002) -
Primary degenerative dementia of the Alzheimer type, presenile onset, with delirium (
65096006) -
Primary degenerative dementia of the Alzheimer type, presenile onset, with delusions (
54502004) -
Primary degenerative dementia of the Alzheimer type, presenile onset, with depression (
10532003) -
Primary degenerative dementia of the Alzheimer type, senile onset (
416975007) -
Primary degenerative dementia of the Alzheimer type, senile onset in remission (
698954005) -
Primary degenerative dementia of the Alzheimer type, senile onset, uncomplicated (
66108005) -
Primary degenerative dementia of the Alzheimer type, senile onset, with delirium (
4817008) -
Primary degenerative dementia of the Alzheimer type, senile onset, with delusions (
55009008) -
Primary degenerative dementia of the Alzheimer type, senile onset, with depression (
26852004) -
Primary hypomagnesemia, generalized seizures, intellectual disability, obesity syndrome (
1351854006) -
Primary hypomagnesemia, refractory seizures, intellectual disability syndrome (
1269236003) -
Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome (
782755007) -
Profound intellectual development disorder with impairment of behaviour (
1089731000000104) -
Profound intellectual development disorder with minimal impairment of behaviour (
1089721000000101) -
Profound intellectual development disorder with significant impairment of behaviour (
1089711000000107) -
Profound intellectual development disorder without impairment of behaviour (
1089701000000105) -
Profound intellectual disability (
31216003) -
Progressive cerebello-cerebral atrophy (
1208481000) -
Progressive epilepsy-intellectual disability syndrome Finnish type (
703526007) -
Progressive essential tremor, speech impairment, facial dysmorphism, intellectual disability, abnormal behavior syndrome (
1260130005) -
Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome (
1187303004) -
Protein kinase cAMP-dependent type I regulatory subunit beta-related neurodegenerative dementia with intermediate filaments (
774069007) -
Protocadherin 19 clustering epilepsy (
716706009) -
Prune belly syndrome with pulmonic stenosis, intellectual disability and deafness (
236529001) -
Prune exopolyphosphatase 1-related neurological syndrome (
1222657001) -
Pseudoleprechaunism syndrome Patterson type (
771262009) -
Pseudoprogeria syndrome (
733086003) -
Psychoactive substance-induced organic dementia (
111480006) -
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (
724039002) -
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (
1260097007) -
Pyrroline-5-carboxylate reductase 1 related de Barsy syndrome (
1295488006) -
Pyrroline-5-carboxylate reductase 2 related microcephaly, progressive leukoencephalopathy (
1237421000) -
RAB18, member RAS oncogene family deficiency (
772225005) -
Radioulnar synostosis with developmental delay and hypotonia syndrome (
721883006) -
Radioulnar synostosis with microcephaly and scoliosis syndrome (
719162001) -
Ramos Arroyo syndrome (
723504000) -
Rapidly progressive dementia (
723390000) -
Rare non-syndromic intellectual disability (
773772001) -
Recognition memory test (
273740006) -
Recognition observable (
363884002) -
Recognition odor (
5987007) -
Recognition, function (
312020002) -
Recognizes self (
225665000) -
Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome (
1172698005) -
Renpenning syndrome (
699669001) -
Residual cognitive deficit as late effect of cerebrovascular accident (
442212003) -
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (
724001005) -
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome (
1220597000) -
Retrograde amnesia (
51921000) -
Retrospective falsification (
26581009) -
Rett syndrome (
68618008) -
Richieri Costa-da Silva syndrome (
782941005) -
Right temporal atrophy variant frontotemporal dementia (
716667005) -
Roifman syndrome (
773404000) -
Route recognition, function (
312021003) -
Rust Inventory of Schizotypal Cognitions (
304767003) -
SET domain containing 2, histone lysine methyltransferase-related microcephaly, severe intellectual disability, multiple congenital anomalies syndrome (
1300119004) -
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily A, member 2-related blepharophimosis, intellectual disability syndrome (
1300198006) -
Sanjad Sakati syndrome (
1197148005) -
Savant syndrome (
432091002) -
Seckel syndrome (
57917004) -
Sedative, hypnotic AND/OR anxiolytic-induced persisting dementia (
59651006) -
Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome (
721207002) -
Seizures and intellectual disability due to hydroxylysinuria syndrome (
723994004) -
Seizures, scoliosis, macrocephaly syndrome (
1187250005) -
Semantic dementia (
230288001) -
Senile and presenile organic psychotic conditions (
268612007) -
Senile dementia (
15662003) -
Senile dementia with delirium (
191461002) -
Senile dementia with delusion (
371024007) -
Senile dementia with depression (
191459006) -
Senile dementia with depressive or paranoid features (
191457008) -
Senile dementia with paranoia (
191458003) -
Senile dementia with psychosis (
371026009) -
Severe X-linked intellectual disability Gustavson type (
722213009) -
Severe cognitive impairment (
702956004) -
Severe feeding difficulties, failure to thrive, microcephaly due to ASXL transcriptional regulator 3 deficiency syndrome (
773400009) -
Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome (
1172629005) -
Severe intellectual development disorder with impairment of behaviour (
1089771000000102) -
Severe intellectual development disorder with minimal impairment of behaviour (
1089761000000109) -
Severe intellectual development disorder with significant impairment of behaviour (
1089751000000106) -
Severe intellectual development disorder without significant impairment of behaviour (
1089741000000108) -
Severe intellectual disability (
40700009) -
Severe intellectual disability and progressive spastic paraplegia (
778011005) -
Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome (
1208727002) -
Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome (
723676007) -
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (
1197591008) -
Severe intellectual disability, poor language, strabismus, grimacing face, long fingers syndrome (
773551001) -
Severe intellectual disability, progressive postnatal microcephaly, midline stereotypic hand movements syndrome (
774149004) -
Severe intellectual disability, progressive spastic diplegia syndrome (
782723007) -
Severe intellectual disability, short stature, behavioral abnormalities, facial dysmorphism syndrome (
773419004) -
Severe microbrachycephaly, intellectual disability, athetoid cerebral palsy syndrome (
783005002) -
Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome (
770751003) -
Severe neurodevelopmental disorder with feeding difficulties, stereotypic hand movement, bilateral cataract (
1179282009) -
Severe oculo-renal-cerebellar syndrome (
1208341008) -
Short stature with webbed neck and congenital heart disease syndrome (
721073008) -
Short stature, brachydactyly, obesity, global developmental delay syndrome (
1187277001) -
Short stature, developmental delay, congenital heart defect syndrome (
1237512003) -
Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome (
1284851009) -
Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome (
726672000) -
Short ulna, dysmorphism, hypotonia, intellectual disability syndrome (
773556006) -
Shprintzen Goldberg craniosynostosis syndrome (
719069008) -
Signal recognition particle immunoglobulin G antibody measurement (
798241000000108) -
Significant intellectual disability (
1239331000000100) -
Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome (
734173003) -
Skeletal dysplasia with epilepsy and short stature syndrome (
715428003) -
Skeletal dysplasia with intellectual disability syndrome (
722478008) -
Skeletal dysplasia, T-cell immunodeficiency, developmental delay syndrome (
1177175008) -
Sodium voltage-gated channel alpha subunit 8 developmental and epileptic encephalopathy (
765170001) -
Solute carrier family 12 member 2-related developmental delay, intellectual disability, sensorineural deafness syndrome (
1367656002) -
Spastic paraplegia with precocious puberty syndrome (
732958004) -
Spastic paraplegia, glaucoma, intellectual disability syndrome (
733455003) -
Spastic paraplegia, intellectual disability, nystagmus, obesity syndrome (
1260134001) -
Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (
722209002) -
Spastic paraplegia, severe developmental delay, epilepsy syndrome (
1187278006) -
Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome (
723621000) -
Spastic tetraplegia, thin corpus callosum, progressive postnatal microcephaly syndrome (
1237418002) -
Special AT-rich sequence-binding protein 2-associated syndrome (
1208488006) -
Spondyloepimetaphyseal dysplasia Genevieve type (
773303005) -
Spondyloepiphyseal dysplasia tarda Kohn type (
719202006) -
Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome (
718766002) -
Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual disability, Leber congenital amaurosis syndrome (
1356736002) -
Spondylometaphyseal dysplasia, corneal dystrophy syndrome (
1269226006) -
Stromal antigen 1-related intellectual disability, facial dysmorphism, gastroesophageal reflux syndrome (
1187041000) -
Subcortical dementia (
762707000) -
Subcortical leukoencephalopathy (
90099008) -
Subcortical vascular dementia (
230286002) -
Synaptic Ras GTPase activating protein 1-related developmental and epileptic encephalopathy (
1222656005) -
Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation (
719161008) -
Syndromic X-linked intellectual disability type 11 (
718900002) -
Syndromic X-linked intellectual disability type 7 (
719160009) -
THO complex 6-related developmental delay, microcephaly, facial dysmorphism syndrome (
773554009) -
Tall stature, intellectual disability, facial dysmorphism syndrome (
768843007) -
Tall stature, intellectual disability, renal anomalies syndrome (
1169359006) -
Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder (
1172626003) -
Temple Baraitser syndrome (
725140007) -
Temporary loss of memory (
162200009) -
Temtamy preaxial brachydactyly syndrome (
777998000) -
Tetrasomy 12p syndrome (
9527009) -
Therapy to promote recognition and understanding of complex phrases (
311629003) -
Therapy to promote recognition and understanding of complex sentences (
311631007) -
Therapy to promote recognition and understanding of concrete words (
311627001) -
Therapy to promote recognition and understanding of conversation (
311633005) -
Therapy to promote recognition and understanding of humor (
311635003) -
Therapy to promote recognition and understanding of long paragraphs (
311632000) -
Therapy to promote recognition and understanding of paralinguistic aspects of speech (
311637006) -
Therapy to promote recognition and understanding of sarcasm (
311636002) -
Therapy to promote recognition and understanding of simple phrases (
311628006) -
Therapy to promote recognition and understanding of simple sentences (
311630008) -
Therapy to promote recognition and understanding of spontaneous speech (
311634004) -
Thumb stiffness, brachydactyly, intellectual disability syndrome (
733117001) -
Toriello Carey syndrome (
722477003) -
Toxic dementia (
722978000) -
Transient epileptic amnesia (
395689002) -
Transient global amnesia (
230736007) -
Trigonocephaly C syndrome (
715409005) -
Trisomy 10p (
717157006) -
Tryptophanyl tRNA synthetase 2, mitochondrial-related combined oxidative phosphorylation defect (
1260128008) -
Unable to recognise generalised pain (
1075601000000109) -
Unable to recognise need for pressure area care (
1075631000000103) -
Unable to recognise own emotional pain and distress (
1075651000000105) -
Unable to recognise own symptoms (
1075551000000106) -
Unable to recognise pain in body part (
1075661000000108) -
Unable to recognize faces (
285171000) -
Unable to recognize faces by sight (
285169000) -
Unable to recognize familiar people (
285774001) -
Unable to recognize objects (
285157008) -
Unable to recognize objects by sight (
285164005) -
Unable to recognize objects by touch (
285161002) -
Unable to recognize odors (
285186006) -
Unable to recognize own fingers (
285791002) -
Unable to recognize parts of own body (
285780009) -
Unable to recognize sounds (
285174008) -
Unable to recognize surroundings (
285177001) -
Unable to recognize warning sounds (
285183003) -
Uncomplicated arteriosclerotic dementia (
191463004) -
Uncomplicated presenile dementia (
191451009) -
Uncomplicated senile dementia (
191449005) -
Uveal coloboma with cleft lip and palate and intellectual disability syndrome (
719042007) -
VPS11 core subunit of CORVET and HOPS complexes-related autosomal recessive hypomyelinating leukodystrophy (
1187249005) -
Van den Bosch syndrome (
733110004) -
Vascular dementia (
429998004) -
Vascular dementia in remission (
698948009) -
Vascular dementia of acute onset (
230285003) -
Vascular dementia with behavioral disturbance (
288631000119104) -
Vascular dementia without behavioral disturbance (
16276361000119109) -
WW domain containing adaptor with coiled-coil-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome (
1187247007) -
Warburg micro syndrome (
772224009) -
Weaver Williams syndrome (
726670008) -
White Sutton syndrome (
772127009) -
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome (
783703004) -
Wiedemann Steiner syndrome (
763618001) -
Wilson Turner syndrome (
719834005) -
Witteveen Kolk syndrome (
1187122000) -
Wolf Hirschhorn syndrome (
718226002) -
World Health Organization Disability Assessment Schedule 2.0 full version cognition domain score (
1104101000000101) -
Worried (
79015004) -
Worried about being a bad father (
225640002) -
Worried about being a bad mother (
225641003) -
Worried about not coping with baby (
225639004) -
X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizure syndrome (
719139003) -
X-linked cerebral, cerebellar, coloboma syndrome (
770604006) -
X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome (
771148008) -
X-linked complicated corpus callosum dysgenesis (
1010630006) -
X-linked female restricted facial dysmorphism, short stature, choanal atresia, intellectual disability (
1172697000) -
X-linked intellectual deficit-dystonia-dysarthria syndrome (
702412005) -
X-linked intellectual developmental disorder Christianson type (
702354007) -
X-linked intellectual disability Abidi type (
719018008) -
X-linked intellectual disability Armfield type (
719017003) -
X-linked intellectual disability Atkin type (
718577005) -
X-linked intellectual disability Cabezas type (
719811001) -
X-linked intellectual disability Cantagrel type (
719016007) -
X-linked intellectual disability Cilliers type (
719013004) -
X-linked intellectual disability Hedera type (
726727003) -
X-linked intellectual disability Miles Carpenter type (
719012009) -
X-linked intellectual disability Nascimento type (
726732002) -
X-linked intellectual disability Pai type (
719011002) -
X-linked intellectual disability Schimke type (
719010001) -
X-linked intellectual disability Seemanova type (
718897009) -
X-linked intellectual disability Shrimpton type (
718905007) -
X-linked intellectual disability Siderius type (
718908009) -
X-linked intellectual disability Snyder type (
702416008) -
X-linked intellectual disability Stevenson type (
718909001) -
X-linked intellectual disability Stocco Dos Santos type (
718910006) -
X-linked intellectual disability Stoll type (
718911005) -
X-linked intellectual disability Turner type (
718912003) -
X-linked intellectual disability Van Esch type (
718914002) -
X-linked intellectual disability Wilson type (
719009006) -
X-linked intellectual disability and epilepsy with progressive joint contracture and facial dysmorphism syndrome (
719155005) -
X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome (
719157002) -
X-linked intellectual disability due to glutamate ionotropic receptor AMPA type subunit 3 mutations (
783702009) -
X-linked intellectual disability hypotonic face syndrome (
1156584007) -
X-linked intellectual disability with acromegaly and hyperactivity syndrome (
719826004) -
X-linked intellectual disability with ataxia and apraxia syndrome (
718845002) -
X-linked intellectual disability with cerebellar hypoplasia syndrome (
719136005) -
X-linked intellectual disability with cubitus valgus and dysmorphism syndrome (
719138006) -
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (
719140001) -
X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome (
719156006) -
X-linked intellectual disability with marfanoid habitus (
422437002) -
X-linked intellectual disability with plagiocephaly syndrome (
719812008) -
X-linked intellectual disability with seizure and psoriasis syndrome (
719810000) -
X-linked intellectual disability, cardiomegaly, congestive heart failure syndrome (
773587008) -
X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome (
1217228004) -
X-linked intellectual disability, craniofacioskeletal syndrome (
773274001) -
X-linked intellectual disability, global development delay, facial dysmorphism, sacral caudal remnant syndrome (
1237420004) -
X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome (
765471005) -
X-linked intellectual disability, hypotonia, movement disorder syndrome (
1254654006) -
X-linked intellectual disability, limb spasticity, retinal dystrophy, arginine vasopressin deficiency (
732246009) -
X-linked intellectual disability, macrocephaly, macroorchidism syndrome (
719825000) -
X-linked intellectual disability, short stature, overweight syndrome (
1255335006) -
X-linked intellectual disability-psychosis-macroorchidism syndrome (
702356009) -
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome (
1197588008) -
X-linked neurodegenerative syndrome Hamel type (
718847005) -
X-linked recessive intellectual disability and macrocephaly with ciliary dysfunction syndrome (
718896000) -
X-linked spasticity, intellectual disability, epilepsy syndrome (
725163002) -
Xq25 microduplication syndrome (
1229872004) -
Xylosyltransferase 1 congenital disorder of glycosylation (
773418007) -
Zechi Ceide syndrome (
773307006) -
[X]Symptoms and signs involving cognition, perception, emotional state and behavior (
207605005) -
[X]Symptoms and signs involving cognition, perception, emotional state and behaviour (
464401000000109) -
de Barsey syndrome (
59252009) -
nudE neurodevelopment protein 1-related microhydranencephaly (
1237462006)
cognitive disorder
Included 25 out of 37 matching concepts.
Show matching concepts
-
Amnestic mild cognitive disorder (
836301008) -
Borderline cognitive developmental delay (
18541000119100) -
Cognitive communication disorder (
716635007) -
Cognitive deficit due to and following cerebrovascular disease (
290621000119101) -
Cognitive deficit due to and following embolic cerebrovascular accident (
690341000119100) -
Cognitive deficit due to and following hemorrhagic cerebrovascular accident (
672571000119109) -
Cognitive deficit due to and following ischemic cerebrovascular accident (
672561000119103) -
Cognitive deficit due to and following nontraumatic intracerebral hemorrhage (
291711000119109) -
Cognitive deficit due to and following nontraumatic subarachnoid hemorrhage (
291621000119109) -
Cognitive developmental delay (
425805004) -
Cognitive disorder (
443265004) -
Cognitive disorder in remission (
698691002) -
Cognitive impairment caused by ethanol (
1234774002) -
Cognitive impairment due to lead toxicity (
1186839009) -
Impaired cognition (
80216008) -
Language-related cognitive disorder (
229676007) -
Mild cognitive disorder (
78521000000105) -
Mild cognitive disorder (
145040006) -
Mild cognitive disorder (
163619002) -
Mild cognitive disorder (
192195008) -
Mild cognitive disorder (
231447009) -
Mild cognitive disorder (
41171000000106) -
Mild cognitive disorder (
140826008) -
Mild neurocognitive disorder (
386805003) -
Neurocognitive disorder (
709073001) -
Neurocognitive disorder suspected (
55261000087107) -
Pervasive developmental disorder with cognitive developmental delay and complete impairment of functional language (
870308001) -
Pervasive developmental disorder with cognitive developmental delay and marked impairment of functional language (
870305003) -
Pervasive developmental disorder with disorder of intellectual development and absence of functional language with loss of previously acquired skills (
870269009) -
Pervasive developmental disorder with disorder of intellectual development and complete impairment of functional language with loss of previously acquired skills (
870270005) -
Pervasive developmental disorder with disorder of intellectual development and complete impairment of functional language without loss of previously acquired skills (
870268001) -
Pervasive developmental disorder with disorder of intellectual development and marked impairment of functional language with loss of previously acquired skills (
870266002) -
Pervasive developmental disorder with disorder of intellectual development and marked impairment of functional language without loss of previously acquired skills (
870267006) -
Pervasive developmental disorder with disorder of intellectual development and pervasive impairment of functional language without loss of previously acquired skills (
870264004) -
Pervasive developmental disorder with disorder of intellectual development with loss of previously acquired skills (
870265003) -
Pervasive developmental disorder with disorder of intellectual development without loss of previously acquired skills (
870262000) -
Residual cognitive deficit as late effect of cerebrovascular accident (
442212003)
cognitive impairment
Included 75 out of 924 matching concepts.
Show matching concepts
-
11p15.4 microduplication syndrome (
770794008) -
11q22.2q22.3 microdeletion syndrome (
1229882003) -
12p12.1 microdeletion syndrome (
778007004) -
12q14 microdeletion syndrome (
719046005) -
13q12.3 microdeletion syndrome (
773547003) -
14q24.1q24.3 microdeletion syndrome (
773494008) -
15q overgrowth syndrome (
771477003) -
17q11.2 microduplication syndrome (
719583002) -
17q24.2 microdeletion syndrome (
1229873009) -
19p13.3 microduplication syndrome (
1229883008) -
19q13.11 microdeletion syndrome (
719599008) -
1p21.3 microdeletion syndrome (
719600006) -
20q11.2 microdeletion syndrome (
1229891004) -
21q22.11q22.12 microdeletion syndrome (
787171006) -
2p13.2 microdeletion syndrome (
770756008) -
2p21 microdeletion syndrome without cystinuria (
770754006) -
2q33.1 microdeletion syndrome (
763062006) -
3-methylglutaconic aciduria type 9 (
1222672002) -
4 A's Test for delirium and cognitive impairment (
1239191000000102) -
4 A's Test for delirium and cognitive impairment score (
1239211000000103) -
4q25 proximal deletion syndrome (
1251452003) -
5-amino-4-imidazole carboxamide ribosiduria (
725289009) -
5p13 microduplication syndrome (
770793002) -
8q24.3 microdeletion syndrome (
1229895008) -
9q21.13 microdeletion syndrome (
1229875002) -
9q31.1q31.3 microdeletion syndrome (
773493002) -
9q33.3q34.11 microdeletion syndrome (
1228886008) -
AT-hook DNA binding motif containing 1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome (
774068004) -
Achalasia microcephaly syndrome (
718573009) -
Acquired language comprehension impairment (
716306006) -
Activity dependent neuroprotector homeobox related multiple congenital anomalies, intellectual disability, autism spectrum disorder (
766824003) -
Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome (
722281001) -
Age-related cognitive decline (
102891000) -
Agenesis of corpus callosum and abnormal genitalia syndrome (
763797003) -
Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome (
722282008) -
Agenesis of corpus callosum, macrocephaly, hypertelorism syndrome (
1208720000) -
Akinetic-rigid form of Huntington's disease (
230301006) -
Alaninuria, microcephaly, dwarfism, enamel hypoplasia, diabetes mellitus syndrome (
733072002) -
Aldehyde dehydrogenase 18 family member A1-related de Barsy syndrome (
1295485009) -
Alopecia and intellectual disability syndrome (
716191002) -
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (
720981000) -
Alopecia, contracture, dwarfism, intellectual disability syndrome (
720979002) -
Alopecia, epilepsy, intellectual disability syndrome Moynahan type (
788417006) -
Alopecia, progressive neurological defect, endocrinopathy syndrome (
770941005) -
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (
734349003) -
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (
720982007) -
Altered behavior due to Pick's disease (
82351000119105) -
Altered behavior in dementia due to Huntington chorea (
82361000119107) -
Alzheimer's disease (
26929004) -
Alzheimer's disease with altered behavior (
97751000119108) -
Alzheimer's disease with delirium (
142011000119109) -
Alzheimer's disease with delusions (
141991000119109) -
Alzheimer's disease with depressed mood (
142001000119106) -
Alzheimer's disease with progressive aphasia (
230280008) -
Alzheimer's disease with psychosis (
1259128002) -
Amelocerebrohypohidrotic syndrome (
109478007) -
Amnesia (
48167000) -
Amnesia for day to day facts (
247607004) -
Amnesia for important personal information (
247611005) -
Amnesia for recent events (
42176003) -
Amnesia for remote events (
6149008) -
Amnestic mild cognitive disorder (
836301008) -
Amyotrophic lateral sclerosis with frontotemporal dementia (
1259124000) -
Amyotrophic lateral sclerosis, parkinsonism, dementia complex (
838276009) -
Amyotrophic lateral sclerosis, parkinsonism, dementia complex of Kii Peninsula (
1259123006) -
Amyotrophic lateral sclerosis, parkinsonism, dementia complex of West New Guinea (
1259121008) -
Angelman syndrome (
76880004) -
Angelman syndrome due to maternal monosomy 15q11q13 (
1162462009) -
Aniridia and intellectual disability syndrome (
720468000) -
Aniridia, renal agenesis, psychomotor retardation syndrome (
733116005) -
Ankyrin 3 related intellectual disability, sleep disturbance syndrome (
787175002) -
Anterior maxillary protrusion, strabismus, intellectual disability syndrome (
1222706005) -
Anterograde amnesia (
88822006) -
Aortic arch anomaly, facial dysmorphism, intellectual disability syndrome (
763615003) -
Aphonia, deafness, retinal dystrophy, bifid halluces, intellectual disability syndrome (
773583007) -
Aplastic anemia, intellectual disability, dwarfism syndrome (
1332385000) -
Arachnodactyly and intellectual disability with facial dysmorphism syndrome (
720502000) -
Arachnodactyly with abnormal ossification and intellectual disability syndrome (
720501007) -
Arginine-glutamic acid dipeptide repeats-related neurodevelopmental syndrome (
1172624000) -
Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy (
1220600004) -
Arteriosclerotic dementia with delirium (
191464005) -
Arteriosclerotic dementia with depression (
191466007) -
Arteriosclerotic dementia with paranoia (
191465006) -
Assessment using 4 A's Test for delirium and cognitive impairment (
1239201000000100) -
Assessment using conversation analysis profile for people with cognitive impairment (
450751006) -
Assessment using conversation analysis profile for people with cognitive impairment (
802261000000107) -
At increased risk for Alzheimer's disease (
1354660007) -
At increased risk for cognitive impairment (
38369006) -
At increased risk of dementia (
698464007) -
Ataxia with deafness and intellectual disability syndrome (
720517001) -
Ataxia, photosensitivity, short stature syndrome (
773769008) -
Atypical hypotonia cystinuria syndrome (
778025006) -
Augmentative and Alternative Communication Therapy Outcome Measure cognitive impairment score (
1064061000000108) -
Aural atresia with multiple congenital anomalies and intellectual disability syndrome (
720748007) -
Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency (
771448004) -
Autism spectrum disorder due to AUTS2 activator of transcription and developmental regulator deficiency (
771512003) -
Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein (
1156789004) -
Autosomal dominant Alzheimer disease due to mutation of presenilin 1 (
1156800008) -
Autosomal dominant Alzheimer disease due to mutation of presenilin 2 (
1156798001) -
Autosomal dominant deafness with onychodystrophy syndrome (
1208614008) -
Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome (
1255319004) -
Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1.4 linker histone, cluster member mutation (
1304277005) -
Autosomal recessive cerebellar ataxia due to CWF19 like cell cycle control factor 1 deficiency (
1237625002) -
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency (
773498006) -
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency (
770898002) -
Autosomal recessive chorioretinopathy and microcephaly syndrome (
770404004) -
Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction (
1186734006) -
Autosomal recessive intellectual disability, motor dysfunction, multiple joint contracture syndrome (
770901001) -
Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome (
771476007) -
Baraitser Winter cerebrofrontofacial syndrome (
1258972007) -
Bardet-Biedl syndrome (
5619004) -
Basel Vanagaite Smirin Yosef syndrome (
1187644009) -
Behavioral disturbance due to multi-infarct dementia (
293671000119109) -
Behavioral variant of frontotemporal dementia (
716994006) -
Biemond syndrome type 2 (
717887003) -
Blepharonasofacial malformation syndrome (
717913006) -
Blepharophimosis, intellectual disability syndrome (
788584007) -
Blepharophimosis, intellectual disability syndrome, Say-Barber-Biesecker-Young-Simpson type (
699298009) -
Blepharophimosis, intellectual disability syndrome, Verloes type (
778009001) -
Blepharophimosis, intellectual disability syndrome/genitopatellar overlap syndrome (
1304113005) -
Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type (
699297004) -
Borderline cognitive developmental delay (
18541000119100) -
Borderline intellectual disability (
77287004) -
Borjeson-Forssman-Lehmann syndrome (
21634003) -
Brachydactyly and preaxial hallux varus syndrome (
732957009) -
Brachydactyly, mesomelia, intellectual disability, heart defect syndrome (
765761009) -
Brachymorphism with onychodysplasia and dysphalangism syndrome (
720573009) -
Brain anomaly, severe intellectual disability, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome (
717945001) -
Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome (
1169355000) -
Branchial dysplasia, intellectual disability, inguinal hernia syndrome (
732961003) -
Branchioskeletogenital syndrome (
719097002) -
Bullous dystrophy macular type (
725589005) -
CK syndrome (
773329005) -
Calcium/calmodulin-dependent serine protein kinase related intellectual disability (
703389002) -
Carboxypeptidase E-related Prader-Willi-like syndrome (
1340175001) -
Case management and Personal Injury Rehabilitation Therapy Outcome Measure cognitive impairment score (
1894911000000108) -
Caudal appendage deafness syndrome (
726621009) -
Central nervous system calcification, deafness, tubular acidosis, anemia syndrome (
726669007) -
Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome (
763344007) -
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (
726031001) -
Cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anemia, growth retardation syndrome (
1332508004) -
Cerebro-facio-thoracic dysplasia (
720635002) -
Cerebrofacioarticular syndrome (
763353000) -
Cerebrooculonasal syndrome (
720855003) -
Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome (
763136000) -
Cherubism with gingival fibromatosis (
389273002) -
Chloride voltage-gated channel 4-related X-linked intellectual disability syndrome (
1172691004) -
Chromodomain helicase DNA binding protein 4-related neurodevelopmental disorder (
1332510002) -
Chromodomain helicase dna-binding protein 3- related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome (
1179408008) -
Chromosome 11p11.2 deletion syndrome (
702346005) -
Chromosome Xp11.3 microdeletion syndrome (
719808002) -
Chronic traumatic encephalopathy (
1187004001) -
Clark Baraitser syndrome (
1300132009) -
Cleft palate with short stature and vertebral anomaly syndrome (
719466009) -
Cleft palate, congenital heart defect, intellectual disability syndrome (
1335869007) -
Clinical Impairment Assessment Cognitive Impairment score (
2119681000000100) -
Coffin-Lowry syndrome (
15182000) -
Coffin-Siris syndrome (
10007009) -
Cognitive changes due to organic disorder (
141601000119107) -
Cognitive communication disorder (
716635007) -
Cognitive deficit due to and following cerebrovascular disease (
290621000119101) -
Cognitive deficit due to and following embolic cerebrovascular accident (
690341000119100) -
Cognitive deficit due to and following hemorrhagic cerebrovascular accident (
672571000119109) -
Cognitive deficit due to and following ischemic cerebrovascular accident (
672561000119103) -
Cognitive deficit due to and following nontraumatic intracerebral hemorrhage (
291711000119109) -
Cognitive deficit due to and following nontraumatic subarachnoid hemorrhage (
291621000119109) -
Cognitive deficit in attention (
142261000119100) -
Cognitive deficit in psychomotor function (
142291000119107) -
Cognitive deficit in visuospatial function (
142281000119109) -
Cognitive developmental delay (
425805004) -
Cognitive disorder (
443265004) -
Cognitive disorder in remission (
698691002) -
Cognitive dysfunction following surgical procedure (
771417007) -
Cognitive impairment caused by ethanol (
1234774002) -
Cognitive impairment caused by ingestible alcohol (
840449007) -
Cognitive impairment co-occurrent and due to human immunodeficiency virus infection (
15928141000119107) -
Cognitive impairment co-occurrent and due to primary psychotic disorder (
724760003) -
Cognitive impairment due to late-delayed irradiation of brain (
1259562009) -
Cognitive impairment due to lead toxicity (
1186839009) -
Cognitive impairment due to toxicity of substance (
762298000) -
Cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, skeletal dysplasia syndrome (
764455002) -
Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome (
720639008) -
Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome (
776204008) -
Combined oxidative phosphorylation defect type 23 (
1173036000) -
Combined oxidative phosphorylation defect type 39 (
1279845005) -
Congenital cataract with ataxia and deafness syndrome (
719102004) -
Congenital cataract with deafness and hypogonadism syndrome (
722378009) -
Congenital cataract with hypertrichosis and intellectual disability syndrome (
722379001) -
Congenital cataract with intellectual disability and anal atresia and urinary defect syndrome (
715989002) -
Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome (
722380003) -
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (
1177169004) -
Congenital contracture of limbs and face, hypotonia, developmental delay syndrome (
1255322002) -
Congenital hypoplasia of ulna and intellectual disability syndrome (
719842006) -
Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome (
1208936008) -
Congenital insensitivity to pain with severe intellectual disability (
1237623009) -
Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome (
1172594000) -
Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome (
782757004) -
Congenital muscular dystrophy with intellectual disability (
783174004) -
Congenital muscular dystrophy with intellectual disability and severe epilepsy (
782772000) -
Congenital pontocerebellar hypoplasia type 11 (
1300188000) -
Congenital pontocerebellar hypoplasia type 14 (
1300192007) -
Contactin associated protein 2-related developmental and epileptic encephalopathy (
1230376005) -
Contracture with ectodermal dysplasia and orofacial cleft syndrome (
720746006) -
Conversation analysis profile for people with cognitive impairment (
450750007) -
Conversation analysis profile for people with cognitive impairment (
802231000000102) -
Cortical blindness, intellectual disability, polydactyly syndrome (
732251003) -
Cortical vascular dementia (
833326008) -
Craniodigital syndrome and intellectual disability syndrome (
763665007) -
Craniofacial digital and genital anomalies syndrome (
716089008) -
Craniofacial dysmorphism with coloboma of eye and corpus callosum agenesis syndrome (
719947004) -
Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome (
1217229007) -
Craniofaciofrontodigital syndrome (
763320005) -
Craniosynostosis, microretrognathia, severe intellectual disability syndrome (
1269224009) -
Cross syndrome (
17827007) -
Cryptorchidism, arachnodactyly, intellectual disability syndrome (
764950001) -
Cyclin K-related neurodevelopmental disorder, severe intellectual disability, facial dysmorphism syndrome (
1332384001) -
Cyclin dependent kinase 13-related congenital heart defects, intellectual disability, facial dysmorphism syndrome (
1299154002) -
Cyclin-dependent kinase-like 5 developmental and epileptic encephalopathy (
773230003) -
Cystic fibrosis with gastritis and megaloblastic anemia syndrome (
720401009) -
Cystic leukoencephalopathy without megalencephaly (
720825005) -
Deafness and intellectual disability Martin Probst type syndrome (
721087008) -
Deafness with onychodystrophy syndrome (
773735007) -
Deafness with skeletal dysplasia and lip granuloma syndrome (
720957007) -
Deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome (
721086004) -
Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (
719800009) -
Deafness-dystonia-optic neuronopathy syndrome (
702423009) -
Delirium co-occurrent with dementia (
725898002) -
Dementia (
52448006) -
Dementia associated with Parkinson's Disease (
425390006) -
Dementia associated with alcoholism (
281004) -
Dementia associated with another disease (
191519005) -
Dementia associated with cerebral anoxia (
698781002) -
Dementia associated with cerebral lipidosis (
698624003) -
Dementia associated with multiple sclerosis (
698626001) -
Dementia associated with neurosyphilis (
698725008) -
Dementia associated with normal pressure hydrocephalus (
698625002) -
Dementia associated with viral encephalitis (
698726009) -
Dementia caused by drug (
191493005) -
Dementia caused by heavy metal exposure (
733184002) -
Dementia caused by ionizing radiation (
1339031006) -
Dementia caused by manganese and/or manganese compound (
1186887004) -
Dementia caused by volatile inhalant (
788898005) -
Dementia co-occurrent and due to Down syndrome (
733194007) -
Dementia co-occurrent and due to Pick's disease (
21921000119103) -
Dementia co-occurrent and due to neurocysticercosis (
722977005) -
Dementia co-occurrent and due to progressive multifocal leukoencephalopathy (
733193001) -
Dementia co-occurrent with human immunodeficiency virus infection (
713844000) -
Dementia due to Behcet syndrome (
1259579003) -
Dementia due to Creutzfeldt Jakob disease (
429458009) -
Dementia due to Gerstmann Straussler Scheinker syndrome (
1259469003) -
Dementia due to Hashimoto encephalopathy (
1259471003) -
Dementia due to Huntington chorea (
442344002) -
Dementia due to Lewy body disease (
1363185006) -
Dementia due to Lyme disease (
1259496000) -
Dementia due to Parkinson's disease (
101421000119107) -
Dementia due to Rett syndrome (
130121000119104) -
Dementia due to Whipple disease (
1259513009) -
Dementia due to Wilson disease (
1259511006) -
Dementia due to acquired hypothyroidism (
1259591007) -
Dementia due to and following dialysis (
1259584009) -
Dementia due to and following injury of head (
762351006) -
Dementia due to atypical pantothenate kinase associated neurodegeneration (
1259679007) -
Dementia due to autoimmune encephalitis (
1259586006) -
Dementia due to carbon monoxide poisoning (
840464007) -
Dementia due to celiac disease (
1259581001) -
Dementia due to cerebral amyloid angiopathy (
1259488005) -
Dementia due to cerebral vasculitis (
1259485008) -
Dementia due to chromosomal anomaly (
722980006) -
Dementia due to chronic intracranial subdural hematoma (
733191004) -
Dementia due to classical pantothenate kinase associated neurodegeneration (
1259990004) -
Dementia due to cobalamin deficiency (
1186880002) -
Dementia due to deficiency of folic acid (
1148924004) -
Dementia due to disorder of central nervous system (
724776007) -
Dementia due to familial Creutzfeldt-Jakob disease (
1259478009) -
Dementia due to fatal familial insomnia (
1259480003) -
Dementia due to fragile X syndrome (
1259473000) -
Dementia due to genetic disease (
1259476008) -
Dementia due to hemorrhagic cerebral infarction due to hypertension (
1259499007) -
Dementia due to hepatic failure (
1259465009) -
Dementia due to herpes encephalitis (
733192006) -
Dementia due to hypercalcemia (
1259467001) -
Dementia due to hypertensive encephalopathy (
1259531005) -
Dementia due to iatrogenic Creutzfeldt-Jakob disease (
1259503001) -
Dementia due to infectious disease (
724777003) -
Dementia due to inflammatory disorder of musculoskeletal system (
1259661008) -
Dementia due to iron deficiency (
840465008) -
Dementia due to kuru (
1259501004) -
Dementia due to leukodystrophy (
1259494002) -
Dementia due to metabolic abnormality (
722979008) -
Dementia due to metastatic malignant neoplasm to brain (
1259492003) -
Dementia due to multiple sclerosis with altered behavior (
82371000119101) -
Dementia due to multiple system atrophy (
1259677009) -
Dementia due to neurofilament inclusion body disease (
1259673008) -
Dementia due to niacin deficiency (
1186881003) -
Dementia due to nutritional deficiency disorder (
1186883000) -
Dementia due to obstructive hydrocephalus (
1259675001) -
Dementia due to paraneoplastic encephalitis (
1259667007) -
Dementia due to pellagra (
788899002) -
Dementia due to polyarteritis nodosa (
1259663006) -
Dementia due to primary malignant neoplasm of brain (
733190003) -
Dementia due to prion disease (
762350007) -
Dementia due to progressive subcortical gliosis (
1259665004) -
Dementia due to renal failure (
1259656006) -
Dementia due to sporadic Creutzfeldt-Jakob disease (
1259529001) -
Dementia due to subacute sclerosing panencephalitis (
1259519008) -
Dementia due to systemic lupus erythematosus (
1259517005) -
Dementia due to thiamine deficiency (
1186879000) -
Dementia due to trypanosomiasis (
1259524006) -
Dementia due to variant Creutzfeldt-Jakob disease (
1259522005) -
Dementia due to vitamin E deficiency (
1186877003) -
Dementia in remission (
698949001) -
Dementia of frontal lobe type (
278857002) -
Dementia of the Alzheimer type with behavioral disturbance (
1581000119101) -
Dementia paralytica juvenilis (
82959004) -
Dementia with acquired immunodeficiency syndrome (
421529006) -
Dementia with behavioral disturbance (
1591000119103) -
Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome (
721089006) -
Developmental and speech delay due to SRY-box 5 deficiency (
771472009) -
Developmental delay with autism spectrum disorder and gait instability (
770790004) -
Developmental delay, facial dysmorphism syndrome due to mediator complex subunit 13 like deficiency (
787093004) -
Developmental delay, language impairment, dopa responsive dystonia, parkinsonism syndrome (
1380254000) -
Diabetes, hypogonadism, deafness, intellectual disability syndrome (
816067005) -
Dialysis dementia (
9345005) -
Dibasic amino aciduria type 1 (
50056009) -
Did not attend mild cognitive impairment review (
1036961000000106) -
Did not attend mild cognitive impairment review (
1036971000000104) -
Diencephalic mesencephalic junction dysplasia (
766871009) -
Digit span forwards performance impaired (
1386319000) -
Digit span reverse performance impaired (
1386320006) -
Disinhibited behavior due to dementia (
789170003) -
Disorder of sex development with intellectual disability syndrome (
719450007) -
Dissociative amnesia (
84209002) -
Dissociative neurological symptom disorder co-occurrent with cognitive impairment (
736314008) -
Disturbance of cognitive learning (
116340000) -
Disturbance of memory for order of events (
416106008) -
Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome (
1179301003) -
Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion (
783619003) -
Dysequilibrium syndrome (
230782004) -
Dysmorphism, short stature, deafness, disorder of sex development syndrome (
733050004) -
Early onset Alzheimer's disease with behavioral disturbance (
105421000119105) -
Early onset dementia due to Lewy body disease (
1363184005) -
Early onset parkinsonism and intellectual disability syndrome (
716107009) -
Early-onset epilepsy, intellectual disability, brain anomalies syndrome (
1172627007) -
Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome (
773548008) -
Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome (
1187042007) -
Ectodermal dysplasia with blindness syndrome (
721208007) -
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (
734017008) -
Encephalopathy due to mitochondrial and peroxisomal fission defect (
1236807002) -
Encephalopathy, intracerebral calcification, retinal degeneration syndrome (
733049004) -
Epidermal growth factor-related primary hypomagnesemia with intellectual disability (
1351962002) -
Epilepsy co-occurrent and due to dementia (
724992007) -
Epilepsy telangiectasia syndrome (
733032006) -
Epilepsy, microcephaly, skeletal dysplasia syndrome (
733031004) -
Epileptic dementia with behavioral disturbance (
82381000119103) -
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (
766870005) -
Equipment Services Therapy Outcome Measure cognitive impairment score (
1064121000000101) -
Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome (
771179007) -
FG syndrome type 1 (
1237179007) -
FRAXE intellectual disability syndrome (
716709002) -
Facial dysmorphism, cleft palate, loose skin syndrome (
763278004) -
Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion (
783061008) -
Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome (
733417008) -
Faciocardiorenal syndrome (
723333000) -
Fallot complex with intellectual disability and growth delay syndrome (
723336008) -
Familial Alzheimer's disease of early onset (
230265002) -
Familial Alzheimer's disease of late onset (
230267005) -
Familial dementia British type (
783161005) -
Familial dementia Danish type (
783258000) -
Familial multiple system deposition of tau protein (
1260328002) -
Fatal X-linked ataxia with deafness and loss of vision (
702441001) -
Fatty acyl-coenzyme A reductase 1 deficiency (
1237619001) -
Fibulin 1-related developmental delay, central nervous system anomaly, syndactyly syndrome (
774070008) -
Filippi syndrome (
720954000) -
Fine Lubinsky syndrome (
720955004) -
Focal Alzheimer's disease (
230269008) -
Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome (
765089003) -
Forgetful (
55533009) -
Forgets to take medication (
1303576005) -
Fragile X syndrome (
613003) -
Fried syndrome (
718848000) -
Frontal lobe degeneration with motor neurone disease (
230274000) -
Frontal variant non-amnestic Alzheimer disease (
1263585001) -
Frontotemporal dementia (
230270009) -
Frontotemporal dementia due to C9orf72 mutation (
1260354005) -
Frontotemporal dementia due to FUS mutation (
1260355006) -
Frontotemporal dementia due to TARDBP mutation (
1260352009) -
Frontotemporal dementia due to VCP mutation (
1260353004) -
Frontotemporal dementia with gene located on 3p11 (
702393003) -
Frontotemporal dementia with parkinsonism-17 (
702429008) -
Fryns Smeets Thiry syndrome (
1208344000) -
G protein subunit beta 5-related intellectual disability, cardiac arrhythmia syndrome (
1186711002) -
GRN-related frontotemporal dementia (
702426001) -
Gabriele-de Vries syndrome (
1186730002) -
General paresis - neurosyphilis (
51928006) -
Genetic intellectual disability (
1362108000) -
Gillespie syndrome (
253176002) -
Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome (
1222658006) -
Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome (
1172630000) -
Glutamate ionotropic receptor NMDA type subunit 2B-related developmental delay, intellectual disability, autism spectrum disorder (
1260195002) -
Glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A developmental and epileptic encephalopathy (
770431001) -
Glutamine rich 1-related intellectual disability, chondrodysplasia syndrome (
1220568003) -
Goldberg Shprintzen megacolon syndrome (
717822006) -
Goniodysgenesis with intellectual disability and short stature syndrome (
716024001) -
Growth delay, intellectual disability, hepatopathy syndrome (
1186713004) -
Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (
721843003) -
Grubben, De Cock, Borghgraef syndrome (
763186006) -
Hair defect with photosensitivity and intellectual disability syndrome (
721007005) -
Hall Riggs syndrome (
721008000) -
Hallucinations co-occurrent and due to late onset dementia (
2421000119107) -
Hao Fountain syndrome (
1360075006) -
Hao Fountain syndrome due to 16p13.2 microdeletion (
1228890005) -
Hennekam lymphangiectasia-lymphedema syndrome (
234146006) -
Hepatic fibrosis, renal cyst, intellectual disability syndrome (
771149000) -
Hereditary cryohydrocytosis with reduced stomatin (
782911008) -
Hereditary persistence of fetal hemoglobin, intellectual disability syndrome (
1360079000) -
HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (
1186724002) -
Human immunodeficiency virus type I enhancer binding protein 2 related intellectual disability (
765434008) -
Huntington's chorea (
58756001) -
Hyperekplexia epilepsy syndrome (
785726009) -
Hyperphosphatasemia with intellectual disability (
33982008) -
Hypogonadism with mitral valve prolapse and intellectual disability syndrome (
721841001) -
Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome (
773553003) -
Hypoplasia of corpus callosum, intellectual disability, adducted thumbs, spasticity, hydrocephalus syndrome (
716996008) -
Hypospadias and intellectual disability syndrome Goldblatt type (
716096005) -
Hypotonia, speech impairment, severe cognitive delay syndrome (
763722004) -
Hypotrichosis and intellectual disability syndrome Lopes type (
723365002) -
Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome (
763404001) -
Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome (
733097003) -
Impaired cognition (
80216008) -
Impaired cognition (
386806002) -
Impaired concentration (
1144748009) -
Impaired environmental interpretation syndrome (
130964008) -
Impaired executive functioning (
736317001) -
Impairment of registration (
283878007) -
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly (
770725000) -
Infantile choroidocerebral calcification syndrome (
724228005) -
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome (
1217371005) -
Infantile inflammatory bowel disease with neurological involvement (
1186721005) -
Infantile multisystem neurologic, endocrine, pancreatic disease (
1260450002) -
Infantile neurodegeneration, progressive spasticity, intellectual disability, white matter lesions syndrome (
1303585005) -
Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome (
782886007) -
Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome (
1260129000) -
Information conversion problem (
76789006) -
Inhalant-induced persisting dementia (
32875003) -
Integral membrane protein 2B related amyloidosis (
1187126002) -
Intellectual development disorder with impairment of behaviour (
1094031000000100) -
Intellectual development disorder with minimal impairment of behaviour (
1094021000000102) -
Intellectual development disorder with significant impairment of behaviour (
1094011000000108) -
Intellectual development disorder without significant impairment of behaviour (
1094001000000106) -
Intellectual disability (
110359009) -
Intellectual disability Birk-Barel type (
764861005) -
Intellectual disability Buenos Aires type (
725906006) -
Intellectual disability Wolff type (
763745005) -
Intellectual disability and short stature with hand contracture and genital anomaly syndrome (
716334004) -
Intellectual disability due to nutritional deficiency (
763626009) -
Intellectual disability with strabismus syndrome (
773405004) -
Intellectual disability, alacrima, achalasia syndrome (
763741001) -
Intellectual disability, aphasia, shuffling gait, adducted thumbs syndrome (
838441009) -
Intellectual disability, autism, speech apraxia, craniofacial dysmorphism syndrome (
1217382002) -
Intellectual disability, balding, patella luxation, acromicria syndrome (
722002002) -
Intellectual disability, brachydactyly, Pierre Robin syndrome (
763744009) -
Intellectual disability, cardiac anomalies, short stature, joint laxity syndrome (
1186729007) -
Intellectual disability, cataract, calcified pinna, myopathy syndrome (
726709001) -
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome (
782753000) -
Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth (
412787009) -
Intellectual disability, craniofacial dysmorphism, cryptorchidism syndrome (
773581009) -
Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome (
722454003) -
Intellectual disability, cupped ears syndrome (
1351837003) -
Intellectual disability, developmental delay, contracture syndrome (
722456001) -
Intellectual disability, early-onset cataract, microcephaly syndrome (
1351838008) -
Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome (
722035007) -
Intellectual disability, epilepsy, bulbous nose syndrome (
721146009) -
Intellectual disability, epilepsy, extrapyramidal syndrome (
1187210007) -
Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome (
722037004) -
Intellectual disability, expressive aphasia, facial dysmorphism syndrome (
1197593006) -
Intellectual disability, facial dysmorphism syndrome due to SET domain containing 5 haploinsufficiency (
782736007) -
Intellectual disability, facial dysmorphism, hand anomalies syndrome (
773416006) -
Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome (
773552008) -
Intellectual disability, hyperkinetic movement, truncal ataxia syndrome (
787174003) -
Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome (
722455002) -
Intellectual disability, hypotonia, brachycephaly, pyloric stenosis, cryptorchidism syndrome (
773621003) -
Intellectual disability, macrocephaly, hypotonia, behavioral abnormalities syndrome (
1254652005) -
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome (
1208746001) -
Intellectual disability, myopathy, short stature, endocrine defect syndrome (
764959000) -
Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome (
763350002) -
Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome (
774102003) -
Intellectual disability, polydactyly, uncombable hair syndrome (
763742008) -
Intellectual disability, seizures, abnormal gait, facial dysmorphism syndrome (
1177167002) -
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome (
770755007) -
Intellectual disability, seizures, macrocephaly, obesity syndrome (
770750002) -
Intellectual disability, severe speech delay, mild dysmorphism syndrome (
774203000) -
Intellectual disability, short stature, hypertelorism syndrome (
771077007) -
Intellectual disability, spasticity, ectrodactyly syndrome (
763743003) -
Intellectual disability, speech delay, dysmorphic features, T cell abnormalities syndrome (
1373748007) -
Intellectual disability, truncal obesity, retinal dystrophy and micropenis syndrome (
715628009) -
Ischemic vascular dementia (
723123001) -
Isodicentric chromosome 15 syndrome (
723332005) -
Jawad syndrome (
771470001) -
Juberg Marsidi syndrome (
721875000) -
Juvenile onset Huntington's disease (
230299004) -
Kagami Ogata syndrome (
770907002) -
Kapur Toriello syndrome (
722031003) -
Keppen Lubinsky syndrome (
1220589007) -
Kleefstra syndrome (
724207001) -
Lack of thinking ability (
110355003) -
Lamb Shaffer syndrome (
1251453008) -
Language-related cognitive disorder (
229676007) -
Laryngeal abductor paralysis with intellectual disability syndrome (
724178000) -
Late onset Alzheimer's dementia with behavioral disturbance (
16219201000119101) -
Late onset Huntington's disease (
230300007) -
Late onset dementia due to Lewy body disease (
312991009) -
Late-onset localized junctional epidermolysis bullosa, intellectual disability syndrome (
773692000) -
Laurence-Moon syndrome (
232059000) -
Lewy body dementia with behavioral disturbance (
135811000119107) -
Lipodystrophy, intellectual disability, deafness syndrome (
721973006) -
Localized dissociative amnesia (
225040001) -
Logopenic non-amnestic Alzheimer disease (
1263555006) -
Lowe syndrome (
79385002) -
Lowry MacLean syndrome (
721974000) -
Lysine demethylase 3B-related intellectual disability, facial dysmorphism, short stature syndrome (
1351843001) -
Macrocephaly and developmental delay syndrome (
763773007) -
Macrocephaly, intellectual disability, autism syndrome (
783089006) -
Macrocephaly, intellectual disability, left ventricular non compaction syndrome (
1187642008) -
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome (
1187304005) -
Macrocephaly, obesity, mental disability, ocular abnormality syndrome (
724137002) -
Macrocephaly, short stature, paraplegia syndrome (
722033000) -
Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome (
1172685001) -
Malan overgrowth syndrome (
763795006) -
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (
722459008) -
Marfanoid habitus with autosomal recessive intellectual disability syndrome (
733062000) -
McDonough syndrome (
715441004) -
Megaconial congenital muscular dystrophy (
1230273004) -
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome (
1260143005) -
Megalocornea with intellectual disability syndrome (
733522005) -
Memory deficit due to and following cerebrovascular accident (
16703661000119105) -
Memory deficit due to and following cerebrovascular disease (
16703551000119107) -
Memory deficit due to and following embolic cerebrovascular accident (
16703711000119100) -
Memory deficit due to and following hemorrhagic cerebrovascular accident (
16703821000119101) -
Memory deficit due to and following ischemic cerebrovascular accident (
16703761000119102) -
Memory deficit due to and following spontaneous intracerebral hemorrhage (
16703491000119101) -
Memory deficit due to and following spontaneous subarachnoid hemorrhage (
16703601000119109) -
Memory impairment (
386807006) -
Memory lapses (
225038006) -
Menke Hennekam syndrome (
1260095004) -
Mesomelic dysplasia, digital anomalies, intellectual disability syndrome (
1363286000) -
Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome (
733419006) -
Metopic ridging, ptosis, facial dysmorphism syndrome (
1179283004) -
Microbrachycephaly, ptosis, cleft lip syndrome (
723403008) -
Microcephalic cortical malformations, short stature due to rotatin deficiency (
1187195007) -
Microcephalic primordial dwarfism Alazami type (
770564004) -
Microcephalic primordial dwarfism Dauber type (
770565003) -
Microcephalic primordial dwarfism Montreal type (
765758008) -
Microcephalus cardiomyopathy syndrome (
719380003) -
Microcephalus with brachydactyly and kyphoscoliosis syndrome (
719378009) -
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome (
764732004) -
Microcephalus, glomerulonephritis, marfanoid habitus syndrome (
733472005) -
Microcephaly with deafness and intellectual disability syndrome (
716112005) -
Microcephaly, corpus callosum and cerebellar vermis hypoplasia, facial dysmorphism, intellectual disability syndrome (
1167375003) -
Microcephaly, corpus callosum hypoplasia, intellectual disability, facial dysmorphism syndrome (
1254650002) -
Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome (
1254651003) -
Microcephaly, seizure, intellectual disability, heart disease syndrome (
723304001) -
Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome (
771074000) -
Microcephaly, thin corpus callosum, intellectual disability syndrome (
770721009) -
Micrognathia, recurrent infections, behavioral abnormalities, mild intellectual disability syndrome (
1187114007) -
Microphthalmia with ankyloblepharon and intellectual disability syndrome (
717222003) -
Microphthalmia with brain atrophy syndrome (
720010009) -
Mild cognitive impairment (
888271000000101) -
Mild cognitive impairment (
888281000000104) -
Mild cognitive impairment annual review (
1052381000000103) -
Mild cognitive impairment review (
1050691000000108) -
Mild cognitive impairment review (
1047041000000108) -
Mild cognitive impairment review declined (
1036901000000107) -
Mild cognitive impairment review declined (
1036911000000109) -
Mild cognitive impairment review first letter (
1036851000000103) -
Mild cognitive impairment review invitation (
1036821000000108) -
Mild cognitive impairment review invitation (
1036831000000105) -
Mild cognitive impairment review invitation first letter (
1036841000000101) -
Mild cognitive impairment review invitation second letter (
1036861000000100) -
Mild cognitive impairment review invitation second letter (
1036871000000107) -
Mild cognitive impairment review invitation third letter (
1036881000000109) -
Mild cognitive impairment review invitation third letter (
1036891000000106) -
Mild intellectual development disorder with impairment of behaviour (
1093991000000101) -
Mild intellectual development disorder with minimal impairment of behaviour (
1089851000000103) -
Mild intellectual development disorder with significant impairment of behaviour (
1089841000000101) -
Mild intellectual development disorder without significant impairment of behaviour (
1089831000000105) -
Mild intellectual disability (
86765009) -
Mild memory disturbance (
192071009) -
Mild neurocognitive disorder (
386805003) -
Minimal cognitive impairment (
110352000) -
Minor memory lapses (
225037001) -
Mixed cortical and subcortical vascular dementia (
230287006) -
Mixed dementia (
79341000119107) -
Mixes past with present (
225039003) -
Moderate cognitive impairment (
888291000000102) -
Moderate cognitive impairment (
702955000) -
Moderate cognitive impairment (
888301000000103) -
Moderate intellectual development disorder with impairment of behaviour (
1089821000000108) -
Moderate intellectual development disorder with minimal impairment of behaviour (
1089811000000102) -
Moderate intellectual development disorder with significant impairment of behaviour (
1089791000000103) -
Moderate intellectual development disorder without significant impairment of behaviour (
1089781000000100) -
Moderate intellectual disability (
61152003) -
Monocarboxylate transporter 8 deficiency (
702327009) -
Mowat-Wilson syndrome (
703535000) -
Mowat-Wilson syndrome due to monosomy 2q22 (
890118006) -
Multi-infarct dementia (
56267009) -
Multi-infarct dementia due to atherosclerosis (
106021000119105) -
Multi-infarct dementia with delirium (
10349009) -
Multi-infarct dementia with delusions (
25772007) -
Multi-infarct dementia with depression (
14070001) -
Multi-infarct dementia, uncomplicated (
70936005) -
Muscle eye brain disease with bilateral multicystic leukodystrophy (
785298001) -
Myelin transcription factor 1 like-related developmental delay, intellectual disability, obesity syndrome (
1303866001) -
Myhre syndrome (
699316006) -
N syndrome (
723410002) -
NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy (
1217379007) -
Neurexin 1-related severe neurodevelopmental disorder, motor stereotypies, chronic constipation, sleep-wake cycle disturbance (
1300131002) -
Neurocognitive disorder (
709073001) -
Neurodevelopmental delay, hypotonia, cerebellar ataxia, cardiac conduction defects syndrome (
1303586006) -
Neurodevelopmental delay, intellectual disability, ataxia, feeding difficulty syndrome (
1363573005) -
Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome (
1217381009) -
Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome (
1222710008) -
Neurofaciodigitorenal syndrome (
725908007) -
Neuronal ceroid lipofuscinosis type 8 (
1373770005) -
Nijmegen breakage syndrome-like disorder (
766753005) -
Non-amnestic Alzheimer disease (
722600006) -
Non-familial Alzheimer's disease of early onset (
230266001) -
Non-familial Alzheimer's disease of late onset (
230268000) -
Non-progressive cerebellar ataxia with intellectual disability (
723441001) -
Non-specific syndromic intellectual disability (
1187038009) -
Noncompliance with medication regimen due to cognitive impairment (
454161000124103) -
Oculocerebrofacial syndrome Kaufman type (
722056009) -
Oculopalatocerebral syndrome (
722055008) -
Ophthalmoplegia, intellectual disability, lingua scrotalis syndrome (
782945001) -
Optic atrophy, intellectual disability syndrome (
770723007) -
Organic amnesia of language (
433081000) -
Organic dementia with acquired immunodeficiency syndrome (
420614009) -
Oro-facial digital syndrome type 10 (
722075004) -
Oro-facial digital syndrome type 11 (
718681002) -
Oro-facial digital syndrome type 14 (
763837007) -
Oro-facial digital syndrome type 5 (
722105002) -
Oro-facial digital syndrome type 8 (
722106001) -
Oro-facial digital syndrome type 9 (
718680001) -
Ossification anomaly with psychomotor developmental delay syndrome (
722107005) -
Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome (
722110003) -
Osteopenia, intellectual disability, sparse hair syndrome (
732954002) -
Pachygyria, intellectual disability, epilepsy syndrome (
763861000) -
Palatal anomalies, widely spaced teeth, facial dysmorphism, developmental delay syndrome (
1172889005) -
Pallister W syndrome (
719020006) -
Paramnesia (
32541007) -
Parkinsonism co-occurrent with dementia of Guadeloupe (
715737004) -
Patchy dementia (
230289009) -
Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease (
765325002) -
Peripheral myelin protein 22-retinoic acid induced 1 contiguous gene duplication syndrome (
1172899000) -
Pervasive developmental disorder with cognitive developmental delay and complete impairment of functional language (
870308001) -
Pervasive developmental disorder with cognitive developmental delay and marked impairment of functional language (
870305003) -
Pervasive developmental disorder with disorder of intellectual development and absence of functional language with loss of previously acquired skills (
870269009) -
Pervasive developmental disorder with disorder of intellectual development and complete impairment of functional language with loss of previously acquired skills (
870270005) -
Pervasive developmental disorder with disorder of intellectual development and complete impairment of functional language without loss of previously acquired skills (
870268001) -
Pervasive developmental disorder with disorder of intellectual development and marked impairment of functional language with loss of previously acquired skills (
870266002) -
Pervasive developmental disorder with disorder of intellectual development and marked impairment of functional language without loss of previously acquired skills (
870267006) -
Pervasive developmental disorder with disorder of intellectual development and pervasive impairment of functional language without loss of previously acquired skills (
870264004) -
Pervasive developmental disorder with disorder of intellectual development with loss of previously acquired skills (
870265003) -
Pervasive developmental disorder with disorder of intellectual development without loss of previously acquired skills (
870262000) -
Phosphodiesterase 4D haploinsufficiency syndrome (
1236843008) -
Phosphoribosylpyrophosphate synthetase superactivity (
723454008) -
Pick's disease with Pick bodies (
230271008) -
Pick's disease with Pick cells and no Pick bodies (
230272001) -
Piebald trait with neurologic defects syndrome (
773984007) -
Pierpont syndrome (
1220594007) -
Pitt-Hopkins syndrome (
702344008) -
Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome (
1208987006) -
Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome (
1167371007) -
Polymicrogyria with optic nerve hypoplasia (
771336003) -
Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome (
770679002) -
Post-traumatic amnesia (
275277000) -
Post-traumatic dementia (
230282000) -
Post-traumatic dementia with behavioral change (
698687007) -
Postaxial polydactyly and intellectual disability syndrome (
721017000) -
Postconcussion syndrome (
40425004) -
Posterior-predominant lissencephaly, broad flat pons and medulla-midline crossing defects syndrome (
1269233006) -
Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome (
1173998003) -
Preaxial polydactyly, colobomata, intellectual disability syndrome (
733088002) -
Predominantly cortical dementia (
1089521000000106) -
Predominantly cortical vascular dementia (
1089531000000108) -
Presenile dementia (
12348006) -
Presenile dementia co-occurrent with human immunodeficiency virus infection (
713488003) -
Presenile dementia with acquired immunodeficiency syndrome (
421023003) -
Presenile dementia with delirium (
191452002) -
Presenile dementia with delusions (
31081000119101) -
Presenile dementia with depression (
191455000) -
Presenile dementia with paranoia (
191454001) -
Presenile dementia with psychosis (
1089501000000102) -
Primary degenerative dementia (
22381000119105) -
Primary degenerative dementia of the Alzheimer type, presenile onset (
416780008) -
Primary degenerative dementia of the Alzheimer type, presenile onset in remission (
698955006) -
Primary degenerative dementia of the Alzheimer type, presenile onset, uncomplicated (
6475002) -
Primary degenerative dementia of the Alzheimer type, presenile onset, with delirium (
65096006) -
Primary degenerative dementia of the Alzheimer type, presenile onset, with delusions (
54502004) -
Primary degenerative dementia of the Alzheimer type, presenile onset, with depression (
10532003) -
Primary degenerative dementia of the Alzheimer type, senile onset (
416975007) -
Primary degenerative dementia of the Alzheimer type, senile onset in remission (
698954005) -
Primary degenerative dementia of the Alzheimer type, senile onset, uncomplicated (
66108005) -
Primary degenerative dementia of the Alzheimer type, senile onset, with delirium (
4817008) -
Primary degenerative dementia of the Alzheimer type, senile onset, with delusions (
55009008) -
Primary degenerative dementia of the Alzheimer type, senile onset, with depression (
26852004) -
Primary hypomagnesemia, generalized seizures, intellectual disability, obesity syndrome (
1351854006) -
Primary hypomagnesemia, refractory seizures, intellectual disability syndrome (
1269236003) -
Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome (
782755007) -
Profound intellectual development disorder with impairment of behaviour (
1089731000000104) -
Profound intellectual development disorder with minimal impairment of behaviour (
1089721000000101) -
Profound intellectual development disorder with significant impairment of behaviour (
1089711000000107) -
Profound intellectual development disorder without impairment of behaviour (
1089701000000105) -
Profound intellectual disability (
31216003) -
Progressive cerebello-cerebral atrophy (
1208481000) -
Progressive epilepsy-intellectual disability syndrome Finnish type (
703526007) -
Progressive essential tremor, speech impairment, facial dysmorphism, intellectual disability, abnormal behavior syndrome (
1260130005) -
Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome (
1187303004) -
Protein kinase cAMP-dependent type I regulatory subunit beta-related neurodegenerative dementia with intermediate filaments (
774069007) -
Protocadherin 19 clustering epilepsy (
716706009) -
Prune belly syndrome with pulmonic stenosis, intellectual disability and deafness (
236529001) -
Prune exopolyphosphatase 1-related neurological syndrome (
1222657001) -
Pseudoleprechaunism syndrome Patterson type (
771262009) -
Pseudoprogeria syndrome (
733086003) -
Psychoactive substance-induced organic dementia (
111480006) -
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (
724039002) -
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (
1260097007) -
Pyrroline-5-carboxylate reductase 1 related de Barsy syndrome (
1295488006) -
Pyrroline-5-carboxylate reductase 2 related microcephaly, progressive leukoencephalopathy (
1237421000) -
RAB18, member RAS oncogene family deficiency (
772225005) -
Radioulnar synostosis with developmental delay and hypotonia syndrome (
721883006) -
Radioulnar synostosis with microcephaly and scoliosis syndrome (
719162001) -
Ramos Arroyo syndrome (
723504000) -
Rapidly progressive dementia (
723390000) -
Rare non-syndromic intellectual disability (
773772001) -
Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome (
1172698005) -
Renpenning syndrome (
699669001) -
Residual cognitive deficit as late effect of cerebrovascular accident (
442212003) -
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (
724001005) -
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome (
1220597000) -
Retrograde amnesia (
51921000) -
Retrospective falsification (
26581009) -
Rett syndrome (
68618008) -
Richieri Costa-da Silva syndrome (
782941005) -
Right temporal atrophy variant frontotemporal dementia (
716667005) -
Roifman syndrome (
773404000) -
SET domain containing 2, histone lysine methyltransferase-related microcephaly, severe intellectual disability, multiple congenital anomalies syndrome (
1300119004) -
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily A, member 2-related blepharophimosis, intellectual disability syndrome (
1300198006) -
Sanjad Sakati syndrome (
1197148005) -
Savant syndrome (
432091002) -
Screening for cognitive impairment not appropriate (
1026071000000102) -
Screening for cognitive impairment not appropriate (
1026081000000100) -
Seckel syndrome (
57917004) -
Sedative, hypnotic AND/OR anxiolytic-induced persisting dementia (
59651006) -
Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome (
721207002) -
Seizures and intellectual disability due to hydroxylysinuria syndrome (
723994004) -
Seizures, scoliosis, macrocephaly syndrome (
1187250005) -
Semantic dementia (
230288001) -
Senile and presenile organic psychotic conditions (
268612007) -
Senile dementia (
15662003) -
Senile dementia with delirium (
191461002) -
Senile dementia with delusion (
371024007) -
Senile dementia with depression (
191459006) -
Senile dementia with depressive or paranoid features (
191457008) -
Senile dementia with paranoia (
191458003) -
Senile dementia with psychosis (
371026009) -
Severe X-linked intellectual disability Gustavson type (
722213009) -
Severe cognitive impairment (
702956004) -
Severe cognitive impairment (
888311000000101) -
Severe cognitive impairment (
888321000000107) -
Severe feeding difficulties, failure to thrive, microcephaly due to ASXL transcriptional regulator 3 deficiency syndrome (
773400009) -
Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome (
1172629005) -
Severe intellectual development disorder with impairment of behaviour (
1089771000000102) -
Severe intellectual development disorder with minimal impairment of behaviour (
1089761000000109) -
Severe intellectual development disorder with significant impairment of behaviour (
1089751000000106) -
Severe intellectual development disorder without significant impairment of behaviour (
1089741000000108) -
Severe intellectual disability (
40700009) -
Severe intellectual disability and progressive spastic paraplegia (
778011005) -
Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome (
1208727002) -
Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome (
723676007) -
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (
1197591008) -
Severe intellectual disability, poor language, strabismus, grimacing face, long fingers syndrome (
773551001) -
Severe intellectual disability, progressive postnatal microcephaly, midline stereotypic hand movements syndrome (
774149004) -
Severe intellectual disability, progressive spastic diplegia syndrome (
782723007) -
Severe intellectual disability, short stature, behavioral abnormalities, facial dysmorphism syndrome (
773419004) -
Severe microbrachycephaly, intellectual disability, athetoid cerebral palsy syndrome (
783005002) -
Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome (
770751003) -
Severe neurodevelopmental disorder with feeding difficulties, stereotypic hand movement, bilateral cataract (
1179282009) -
Severe oculo-renal-cerebellar syndrome (
1208341008) -
Short stature with webbed neck and congenital heart disease syndrome (
721073008) -
Short stature, brachydactyly, obesity, global developmental delay syndrome (
1187277001) -
Short stature, developmental delay, congenital heart defect syndrome (
1237512003) -
Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome (
1284851009) -
Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome (
726672000) -
Short ulna, dysmorphism, hypotonia, intellectual disability syndrome (
773556006) -
Shprintzen Goldberg craniosynostosis syndrome (
719069008) -
Significant intellectual disability (
1239331000000100) -
Six Item Cognitive Impairment Test (
1085141000000105) -
Six Item Cognitive Impairment Test total score (
1085151000000108) -
Six item cognitive impairment test (
100851000000102) -
Six item cognitive impairment test (
95991000000104) -
Six item cognitive impairment test (
408492009) -
Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome (
734173003) -
Skeletal dysplasia with epilepsy and short stature syndrome (
715428003) -
Skeletal dysplasia with intellectual disability syndrome (
722478008) -
Skeletal dysplasia, T-cell immunodeficiency, developmental delay syndrome (
1177175008) -
Sodium voltage-gated channel alpha subunit 8 developmental and epileptic encephalopathy (
765170001) -
Solute carrier family 12 member 2-related developmental delay, intellectual disability, sensorineural deafness syndrome (
1367656002) -
Spastic paraplegia with precocious puberty syndrome (
732958004) -
Spastic paraplegia, glaucoma, intellectual disability syndrome (
733455003) -
Spastic paraplegia, intellectual disability, nystagmus, obesity syndrome (
1260134001) -
Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (
722209002) -
Spastic paraplegia, severe developmental delay, epilepsy syndrome (
1187278006) -
Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome (
723621000) -
Spastic tetraplegia, thin corpus callosum, progressive postnatal microcephaly syndrome (
1237418002) -
Special AT-rich sequence-binding protein 2-associated syndrome (
1208488006) -
Spondyloepimetaphyseal dysplasia Genevieve type (
773303005) -
Spondyloepiphyseal dysplasia tarda Kohn type (
719202006) -
Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome (
718766002) -
Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual disability, Leber congenital amaurosis syndrome (
1356736002) -
Spondylometaphyseal dysplasia, corneal dystrophy syndrome (
1269226006) -
Stromal antigen 1-related intellectual disability, facial dysmorphism, gastroesophageal reflux syndrome (
1187041000) -
Subcortical dementia (
762707000) -
Subcortical leukoencephalopathy (
90099008) -
Subcortical vascular dementia (
230286002) -
Synaptic Ras GTPase activating protein 1-related developmental and epileptic encephalopathy (
1222656005) -
Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation (
719161008) -
Syndromic X-linked intellectual disability type 11 (
718900002) -
Syndromic X-linked intellectual disability type 7 (
719160009) -
THO complex 6-related developmental delay, microcephaly, facial dysmorphism syndrome (
773554009) -
Tall stature, intellectual disability, facial dysmorphism syndrome (
768843007) -
Tall stature, intellectual disability, renal anomalies syndrome (
1169359006) -
Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder (
1172626003) -
Temple Baraitser syndrome (
725140007) -
Temporary loss of memory (
162200009) -
Temtamy preaxial brachydactyly syndrome (
777998000) -
Tetrasomy 12p syndrome (
9527009) -
Thumb stiffness, brachydactyly, intellectual disability syndrome (
733117001) -
Toriello Carey syndrome (
722477003) -
Toxic dementia (
722978000) -
Transient epileptic amnesia (
395689002) -
Transient global amnesia (
230736007) -
Trigonocephaly C syndrome (
715409005) -
Trisomy 10p (
717157006) -
Tryptophanyl tRNA synthetase 2, mitochondrial-related combined oxidative phosphorylation defect (
1260128008) -
Uncomplicated arteriosclerotic dementia (
191463004) -
Uncomplicated presenile dementia (
191451009) -
Uncomplicated senile dementia (
191449005) -
Uveal coloboma with cleft lip and palate and intellectual disability syndrome (
719042007) -
VPS11 core subunit of CORVET and HOPS complexes-related autosomal recessive hypomyelinating leukodystrophy (
1187249005) -
Van den Bosch syndrome (
733110004) -
Vascular dementia (
429998004) -
Vascular dementia in remission (
698948009) -
Vascular dementia of acute onset (
230285003) -
Vascular dementia with behavioral disturbance (
288631000119104) -
Vascular dementia without behavioral disturbance (
16276361000119109) -
WW domain containing adaptor with coiled-coil-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome (
1187247007) -
Warburg micro syndrome (
772224009) -
Weaver Williams syndrome (
726670008) -
White Sutton syndrome (
772127009) -
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome (
783703004) -
Wiedemann Steiner syndrome (
763618001) -
Wilson Turner syndrome (
719834005) -
Witteveen Kolk syndrome (
1187122000) -
Wolf Hirschhorn syndrome (
718226002) -
X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizure syndrome (
719139003) -
X-linked cerebral, cerebellar, coloboma syndrome (
770604006) -
X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome (
771148008) -
X-linked complicated corpus callosum dysgenesis (
1010630006) -
X-linked female restricted facial dysmorphism, short stature, choanal atresia, intellectual disability (
1172697000) -
X-linked intellectual deficit-dystonia-dysarthria syndrome (
702412005) -
X-linked intellectual developmental disorder Christianson type (
702354007) -
X-linked intellectual disability Abidi type (
719018008) -
X-linked intellectual disability Armfield type (
719017003) -
X-linked intellectual disability Atkin type (
718577005) -
X-linked intellectual disability Cabezas type (
719811001) -
X-linked intellectual disability Cantagrel type (
719016007) -
X-linked intellectual disability Cilliers type (
719013004) -
X-linked intellectual disability Hedera type (
726727003) -
X-linked intellectual disability Miles Carpenter type (
719012009) -
X-linked intellectual disability Nascimento type (
726732002) -
X-linked intellectual disability Pai type (
719011002) -
X-linked intellectual disability Schimke type (
719010001) -
X-linked intellectual disability Seemanova type (
718897009) -
X-linked intellectual disability Shrimpton type (
718905007) -
X-linked intellectual disability Siderius type (
718908009) -
X-linked intellectual disability Snyder type (
702416008) -
X-linked intellectual disability Stevenson type (
718909001) -
X-linked intellectual disability Stocco Dos Santos type (
718910006) -
X-linked intellectual disability Stoll type (
718911005) -
X-linked intellectual disability Turner type (
718912003) -
X-linked intellectual disability Van Esch type (
718914002) -
X-linked intellectual disability Wilson type (
719009006) -
X-linked intellectual disability and epilepsy with progressive joint contracture and facial dysmorphism syndrome (
719155005) -
X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome (
719157002) -
X-linked intellectual disability due to glutamate ionotropic receptor AMPA type subunit 3 mutations (
783702009) -
X-linked intellectual disability hypotonic face syndrome (
1156584007) -
X-linked intellectual disability with acromegaly and hyperactivity syndrome (
719826004) -
X-linked intellectual disability with ataxia and apraxia syndrome (
718845002) -
X-linked intellectual disability with cerebellar hypoplasia syndrome (
719136005) -
X-linked intellectual disability with cubitus valgus and dysmorphism syndrome (
719138006) -
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (
719140001) -
X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome (
719156006) -
X-linked intellectual disability with marfanoid habitus (
422437002) -
X-linked intellectual disability with plagiocephaly syndrome (
719812008) -
X-linked intellectual disability with seizure and psoriasis syndrome (
719810000) -
X-linked intellectual disability, cardiomegaly, congestive heart failure syndrome (
773587008) -
X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome (
1217228004) -
X-linked intellectual disability, craniofacioskeletal syndrome (
773274001) -
X-linked intellectual disability, global development delay, facial dysmorphism, sacral caudal remnant syndrome (
1237420004) -
X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome (
765471005) -
X-linked intellectual disability, hypotonia, movement disorder syndrome (
1254654006) -
X-linked intellectual disability, limb spasticity, retinal dystrophy, arginine vasopressin deficiency (
732246009) -
X-linked intellectual disability, macrocephaly, macroorchidism syndrome (
719825000) -
X-linked intellectual disability, short stature, overweight syndrome (
1255335006) -
X-linked intellectual disability-psychosis-macroorchidism syndrome (
702356009) -
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome (
1197588008) -
X-linked neurodegenerative syndrome Hamel type (
718847005) -
X-linked recessive intellectual disability and macrocephaly with ciliary dysfunction syndrome (
718896000) -
X-linked spasticity, intellectual disability, epilepsy syndrome (
725163002) -
Xq25 microduplication syndrome (
1229872004) -
Xylosyltransferase 1 congenital disorder of glycosylation (
773418007) -
Zechi Ceide syndrome (
773307006) -
de Barsey syndrome (
59252009) -
nudE neurodevelopment protein 1-related microhydranencephaly (
1237462006)
forget
Included 14 out of 25 matching concepts.
Show matching concepts
-
Age-associated memory impairment (
231448004) -
Alethia (
102941003) -
Assessment using Car, Relax, Alone, Forget, Family/Friends, Trouble interview version 2.1 (
163841000000105) -
Assessment using Car, Relax, Alone, Forget, Friends, Trouble Screening Test (
868187001) -
Car, Relax, Alone, Forget, Family/Friends, Trouble interview version 2.1 (
153601000000102) -
Car, Relax, Alone, Forget, Family/Friends, Trouble interview version 2.1 score (
163851000000108) -
Car, Relax, Alone, Forget, Friends, Trouble Screening Test (
736042002) -
Car, Relax, Alone, Forget, Friends, Trouble Screening Test version 2.0 (
736043007) -
Forgetful (
55533009) -
Forgetful (
140828009) -
Forgetful (
163621007) -
Forgets recent activities (
247595006) -
Forgets to complete personal care (
423864004) -
Forgets to take medication (
1303576005) -
Forgets what has just done (
247596007) -
Forgets what has just heard (
247600002) -
Forgets what has just read (
247598008) -
Forgets what has just said (
247597003) -
Forgets what has just seen (
247599000) -
Forgets what was going to do (
247593004) -
Forgets what was going to say (
247594005) -
Patient forgets to take medication (
104771000000108) -
Patient forgets to take medication (
107311000000108) -
Patient forgets to take medication (
408367005) -
Repression through forgetting (
224991005)
memory
Included 116 out of 513 matching concepts.
Show matching concepts
-
Ability to manage medication using memory technique (
1137423001) -
Ability to recall five digit number at five minutes (
283887003) -
Ability to recall random address at five minutes (
283886007) -
Ability to remember current year (
285195003) -
Ability to remember day of the week (
283894000) -
Ability to remember faces (
285226002) -
Ability to remember month of year (
283895004) -
Ability to remember motor skills (
283899005) -
Ability to remember name of current prime minister (
283897007) -
Ability to remember name of reigning monarch (
283896003) -
Ability to remember new motor skills (
283900000) -
Ability to remember objects (
283991009) -
Ability to remember old motor skills (
283901001) -
Ability to remember own age (
283893006) -
Ability to remember own date of birth (
283891008) -
Ability to remember sounds (
283898002) -
Ability to remember to eat (
1179213005) -
Ability to remember to infuse enteral nutrition (
1216952008) -
Ability to remember to infuse parenteral nutrition (
1216953003) -
Ability to remember today's date (
285204003) -
Ability to reproduce geometric figure at five minutes (
283889000) -
Able to manage medication regime using memory technique (
1137421004) -
Able to recall five digit number at five minutes (
285211004) -
Able to recall random address at five minutes (
285207005) -
Able to remember current year (
285196002) -
Able to remember day of the week (
285190008) -
Able to remember faces (
285227006) -
Able to remember month of year (
285193005) -
Able to remember motor skills (
285218005) -
Able to remember name of current prime minister (
285199009) -
Able to remember name of reigning monarch (
285198001) -
Able to remember new motor skills (
285220008) -
Able to remember objects (
285224004) -
Able to remember old motor skills (
285222000) -
Able to remember own age (
285189004) -
Able to remember own date of birth (
285187002) -
Able to remember past events (
721157004) -
Able to remember people (
716442002) -
Able to remember places (
719731006) -
Able to remember routines (
719747008) -
Able to remember sounds (
285229009) -
Able to remember today's date (
285205002) -
Able to reproduce geometric figure at five minutes (
285209008) -
Abnormal macrophage (
127565009) -
Addenbrooke's Cognitive Examination-III memory score (
2304541000000104) -
Addenbrooke's cognitive examination revised - memory subscale (
775071000000105) -
Addenbrooke's cognitive examination revised - memory subscore (
711091000000103) -
Addenbrooke's cognitive examination revised memory subscale (
473313006) -
Addenbrooke's cognitive examination revised memory subscore (
770621000000105) -
Age-associated memory impairment (
231448004) -
Alethia (
102941003) -
Amnesia (
48167000) -
Amnesia for day to day facts (
247607004) -
Amnesia for important personal information (
247611005) -
Amnesia for recent events (
42176003) -
Amnesia for remote events (
6149008) -
Anterograde amnesia (
88822006) -
Anxiety about loss of memory (
323331000000106) -
Anxiety about loss of memory (
431432003) -
Armed macrophage (
86373002) -
Assessment of memory (
1199901000168108) -
Assessment using Addenbrooke's cognitive examination revised - memory subscale (
775131000000107) -
Assessment using Addenbrooke's cognitive examination revised memory subscale (
473307002) -
Assessment using Autobiographical Memory Interview (
1097211000000105) -
Assessment using Everyday Memory Questionnaire (
716171009) -
Assessment using Everyday Memory Questionnaire (
973971000000104) -
Assessment using Rivermead Behavioral Memory Test - Third Edition (
982581000000109) -
Assessment using Rivermead Behavioral Memory Test Third Edition (
718696003) -
Assessment using Rivermead Behavioral Memory Test for Children (
718695004) -
Assessment using Rivermead Behavioural Memory Test for Children (
1048681000000106) -
Assessment using Rivermead behavioral memory test (
445797000) -
Assessment using Rivermead behavioural memory test (
712561000000109) -
Assessment using Test Your Memory test (
763124006) -
Assessment using Test Your Memory test (
1084811000000101) -
Assessment: [mental disability] or [memory] or [dementia] (
165277000) -
Association for neuropsychological research and development prospective memory test (
311483006) -
Auditory memory (
283924008) -
Auditory memory therapy (
311606006) -
Autobiographical Memory Interview Autobiographical Incidents Schedule score (
1097231000000102) -
Autobiographical Memory Interview Background Personal Semantic score (
1097241000000106) -
Autobiographical Memory Interview Total Personal Semantic score (
1098421000000102) -
Autobiographical memory (
283996004) -
Autobiographical memory interview (
273296003) -
B lymphocyte (
112130006) -
B lymphocyte positive for CD19 antigen (
115417009) -
Blessed dementia rating scale (
273323004) -
Cannot remember birth dates of children (
247615001) -
Cannot remember name of school (
247616000) -
Cannot remember names of intimates (
247612003) -
Cannot remember wedding anniversary (
247614002) -
Characteristic of immediate recall (
363890003) -
Clone (
47308002) -
Cognitive linguistic quick test memory domain (
863961000000106) -
Committed cell (
55484008) -
Confabulation (
17842005) -
Cytotoxic T lymphocyte (
420638008) -
Delayed verbal memory (
311533004) -
Delusional memories (
276244009) -
Difficulty in remembering dates (
275278005) -
Difficulty remembering past events (
1070821000000108) -
Difficulty remembering people (
1070831000000105) -
Difficulty remembering places (
1068951000000102) -
Difficulty remembering routines (
1070841000000101) -
Digit span forwards performance impaired (
1386319000) -
Digit span forwards performance normal (
1386318008) -
Digit span performance (
283884005) -
Digit span reverse performance impaired (
1386320006) -
Digit span reverse performance normal (
1386321005) -
Dissociative amnesia (
84209002) -
Distortion of memory (
225036005) -
Disturbance of memory for order of events (
416106008) -
Disturbance of memory for order of events (
190001000000109) -
Disturbance of memory for order of events (
186561000000101) -
Does not remember past events (
1072501000000101) -
Does not remember people (
1072511000000104) -
Does not remember places (
1072521000000105) -
Does not remember routines (
1069191000000104) -
Does remember past events (
1074151000000101) -
Does remember people (
1074161000000103) -
Does remember places (
1069441000000100) -
Does remember routines (
1074171000000105) -
Déjà entendu (
49229003) -
Déjà pensé (
21001001) -
Déjà vu (
313005) -
Education for memory impairment (
20991000175106) -
Eidetic images (
112090005) -
Episodic memory, function (
311553000) -
Everyday Memory Questionnaire score (
973981000000102) -
Everyday Memory Questionnaire score (
717829002) -
Everyday memory questionnaire (
311406000) -
Explicit memory (
283910009) -
External memory aids training (
311884008) -
Extremely efficient use of mnemonics (
247603000) -
False memories (
283997008) -
False recognition (
85173004) -
Family history of amnesia (
430728001) -
Fantastical confabulation (
283881002) -
Fat-laden macrophage (
13901007) -
Finding of digit span performance (
365848007) -
Finding of long-term memory performance (
365888002) -
Finding of memory for address recall (
365916007) -
Finding of memory for counting down (
365915006) -
Finding of memory for important event (
365913004) -
Finding of memory for important person (
365914005) -
Finding of memory for months of year in reverse (
1034891000000102) -
Finding of memory for own age (
365906004) -
Finding of memory for own date of birth (
365911002) -
Finding of memory for present month (
365912009) -
Finding of memory for present place (
365908003) -
Finding of memory for present time (
365907008) -
Finding of memory for present year (
365909006) -
Finding of memory form (
365917003) -
Finding of memory performance (
283882009) -
Finding of semantic memory (
365918008) -
Finding of semantic memory performance (
365890001) -
Finding of short-term memory performance (
365859003) -
Finding of type of memories (
365920006) -
Finding of use of memory retrieval aids (
365905000) -
Finding of verbal memory (
365919000) -
Finding of verbal short-term memory performance (
365869009) -
Finding of visual short-term memory performance (
365886003) -
Finding related to ability to recall five digit number at five minutes (
365885004) -
Finding related to ability to recall random address at five minutes (
365875000) -
Finding related to ability to remember current year (
365896007) -
Finding related to ability to remember day of the week (
365893004) -
Finding related to ability to remember faces (
365900005) -
Finding related to ability to remember month of year (
365895006) -
Finding related to ability to remember motor skills (
365902002) -
Finding related to ability to remember name of current prime minister (
365898008) -
Finding related to ability to remember name of reigning monarch (
365897003) -
Finding related to ability to remember new motor skills (
365903007) -
Finding related to ability to remember objects (
365899000) -
Finding related to ability to remember old motor skills (
365904001) -
Finding related to ability to remember own age (
365892009) -
Finding related to ability to remember own date of birth (
365891002) -
Finding related to ability to remember sounds (
365901009) -
Finding related to ability to remember today's date (
365894005) -
Finding related to ability to reproduce geometric figure at five minutes (
365887007) -
Finding relating to immediate recall (
283883004) -
Finding relating to reminiscing (
225042009) -
Flashback due to and following trauma (
1303411009) -
Flashbacks have stopped (
416687002) -
Focal onset cognitive epileptic seizure with memory impairment (
1284865006) -
Follicular dendritic cell (
56685008) -
Forbidden clone (
24309006) -
Forgetful (
55533009) -
Forgets recent activities (
247595006) -
Forgets to complete personal care (
423864004) -
Forgets to take medication (
1303576005) -
Forgets what has just done (
247596007) -
Forgets what has just heard (
247600002) -
Forgets what has just read (
247598008) -
Forgets what has just said (
247597003) -
Forgets what has just seen (
247599000) -
Forgets what was going to do (
247593004) -
Forgets what was going to say (
247594005) -
Fuld object memory evaluation (
304729001) -
Gaucher cell (
16216007) -
Gaucher-like cell (
59870003) -
Graham-Kendall memory for designs test (
273493008) -
Granular null cell (
67124000) -
Hand-Schüller-Christian histiocyte (
123635008) -
Has delayed recall (
283902008) -
Health of the Nation Outcome Scales for People with Learning Disabilities rating scale 5 - memory and orientation (
985481000000104) -
Health of the Nation Outcome Scales for People with Learning Disabilities rating scale 5 score - memory and orientation (
987841000000100) -
Helper T cell (
29594005) -
Helper cell (
7944005) -
Hemosiderin-laden macrophage (
81236001) -
Hunter-Hurler cell (
84702007) -
Hybridoma (
25326005) -
Hypermnesia (
55050000) -
Immature plasma cell (
117293008) -
Immediate memory, function (
69262000) -
Immediate verbal memory (
311532009) -
Immune effector cell (
86224008) -
Immunoglobulin A B lymphocyte (
115603005) -
Immunoglobulin D B lymphocyte (
115604004) -
Immunoglobulin E B lymphocyte (
115605003) -
Immunoglobulin G B lymphocyte (
115606002) -
Immunoglobulin M B lymphocyte (
115607006) -
Immunologic cell (
64419002) -
Immunologic memory, function (
19993006) -
Impairment of registration (
283878007) -
Implicit memory (
283912001) -
Initial memory assessment (
888901000000102) -
Initial memory assessment (
888911000000100) -
Initial memory assessment declined (
890411000000106) -
Initial memory assessment declined (
888881000000100) -
Injection pen with digital memory (
426645000) -
Interdigitating cell (
24333000) -
Intrusive memories (
283989001) -
Isolated memory skills (
276294005) -
Jamais vu (
28249008) -
Kupffer cell (
256002) -
Lipid histiocyte (
76237002) -
Localized dissociative amnesia (
225040001) -
Logical memory paragraph recall (
273579003) -
Long-term memory performance (
247586003) -
Long-term memory within normal limits (
247587007) -
Lymphocyte antigen CD45RO (
86076000) -
Lymphocyte positive for CD8 antigen (
117539009) -
Macrophage (
58986001) -
Mast cell (
6445007) -
Memories (
225035009) -
Memory aided by use of diary (
285215008) -
Memory aided by use of labels (
285214007) -
Memory aided by use of lists (
285213001) -
Memory assessment (
272051008) -
Memory assessment finding (
247618004) -
Memory assistive training device (
463270002) -
Memory deficit due to and following cerebrovascular accident (
16703661000119105) -
Memory deficit due to and following cerebrovascular disease (
16703551000119107) -
Memory deficit due to and following embolic cerebrovascular accident (
16703711000119100) -
Memory deficit due to and following hemorrhagic cerebrovascular accident (
16703821000119101) -
Memory deficit due to and following ischemic cerebrovascular accident (
16703761000119102) -
Memory deficit due to and following spontaneous intracerebral hemorrhage (
16703491000119101) -
Memory deficit due to and following spontaneous subarachnoid hemorrhage (
16703601000119109) -
Memory disorder co-occurrent and due to organic brain damage (
140621000119106) -
Memory disturbance (& amnesia (& symptom)) (
139484009) -
Memory disturbance (& amnesia (& symptom)) (
162199006) -
Memory disturbance: [mild] (
268792003) -
Memory disturbance: [mild] (
154961004) -
Memory finding (
106136008) -
Memory form (
283904009) -
Memory function (
303116000) -
Memory function normal (
247601003) -
Memory function normal (
808991000000105) -
Memory function normal (
247602005) -
Memory impairment (
386807006) -
Memory impairment (
990531000000107) -
Memory impairment (
78461004) -
Memory lapses (
225038006) -
Memory loss care (
408899008) -
Memory loss care assessment (
408902006) -
Memory loss care education (
408900003) -
Memory loss care management (
408901004) -
Memory observable (
363887009) -
Memory observations (
186541000000102) -
Memory observations (
189981000000108) -
Memory performance (
363888004) -
Memory recall (
363889007) -
Memory recall finding (
225033002) -
Memory recall normal (
302294002) -
Memory retraining (
228551009) -
Memory skills training (
302262007) -
Memory test observable (
363891004) -
Memory, function (
13108000) -
Memory-alloy orthopedic fixation plate (
701166006) -
Memory-alloy patella fixation grip (
463443006) -
Memory: address recall (
142716004) -
Memory: address recall success (
142717008) -
Memory: address recall success (
165307002) -
Memory: address recall unsucc. (
142718003) -
Memory: address recall unsuccessful (
165308007) -
Memory: count down (
142712002) -
Memory: count down successful (
165304009) -
Memory: count down successful (
142714001) -
Memory: count down unsuccess. (
142715000) -
Memory: count down unsuccessful (
165305005) -
Memory: import.person not knwn (
142710005) -
Memory: important event (
142706007) -
Memory: important event known (
142708008) -
Memory: important event known (
165299008) -
Memory: important event not kn (
142707003) -
Memory: important event not known (
165298000) -
Memory: important person (
142709000) -
Memory: important person known (
142711009) -
Memory: important person known (
165302008) -
Memory: important person not known (
165301001) -
Memory: months of year in reverse (
1034881000000104) -
Memory: months of year in reverse successful (
1034901000000101) -
Memory: months of year in reverse successful (
1034911000000104) -
Memory: months of year in reverse unsuccessful (
1034921000000105) -
Memory: months of year in reverse unsuccessful (
1034931000000107) -
Memory: own DOB (
142700001) -
Memory: own DOB known (
142702009) -
Memory: own DOB not known (
142701002) -
Memory: own age (
142688004) -
Memory: own age known (
165281000) -
Memory: own age known (
142690003) -
Memory: own age not known (
142689007) -
Memory: own age not known (
165280004) -
Memory: own date of birth known (
165293009) -
Memory: own date of birth not known (
165292004) -
Memory: present month (
142703004) -
Memory: present month known (
165296001) -
Memory: present month known (
142705006) -
Memory: present month not known (
165295002) -
Memory: present month not knwn (
142704005) -
Memory: present place (
142694007) -
Memory: present place known (
142696009) -
Memory: present place known (
165287001) -
Memory: present place not known (
165286005) -
Memory: present place not knwn (
142695008) -
Memory: present time (
142691004) -
Memory: present time known (
165284008) -
Memory: present time known (
142693001) -
Memory: present time not known (
165283002) -
Memory: present time not known (
142692006) -
Memory: present year (
142697000) -
Memory: present year known (
165290007) -
Memory: present year known (
142699002) -
Memory: present year not known (
142698005) -
Memory: present year not known (
165289003) -
Mild memory disturbance (
192071009) -
Mini-Addenbrooke's Cognitive Examination memory score (
2304631000000109) -
Minor memory lapses (
225037001) -
Mixes past with present (
225039003) -
Momentary confabulation (
283880001) -
Mott plasma cell (
83718009) -
NHS Health Check raising awareness about dementia and memory clinics (
871001000000102) -
National Health Service Health Check raising awareness about dementia and memory clinics (
870991000000101) -
Natural killer cell (
259717003) -
Neuropsychology test of memory (
236071000000107) -
Neuropsychology test of memory (
271661000000102) -
Niemann-Pick cell (
9240003) -
Non-lipid histiocyte (
42766006) -
Null lymphocyte (
54991005) -
Organic amnesia of language (
433081000) -
Organic memory impairment (
192072002) -
Paramnesia (
32541007) -
Patient monitoring system module, data memory (
463081005) -
Percent count of non-switched memory B lymphocytes in blood (
53001000237101) -
Percent count of switched memory B lymphocytes in blood (
52931000237101) -
Plasma cell (
113335003) -
Plasmablast (
2579009) -
Pleasant memories (
283990005) -
Polyploid plasmablast (
55093000) -
Poor auditory sequential memory (
413089005) -
Poor auditory sequential memory (
111491000000103) -
Poor auditory sequential memory (
117941000000108) -
Poor long-term memory (
247588002) -
Poor short-term memory (
247592009) -
Poor short-term memory (
808311000000102) -
Poor visual sequential memory (
117931000000104) -
Poor visual sequential memory (
111481000000100) -
Poor visual sequential memory (
413088002) -
Post-traumatic amnesia (
275277000) -
Pre-B lymphocyte (
25841003) -
Procedural memory (
283927001) -
Promotion of use of memory skills (
710125008) -
Proplasmacyte (
24884008) -
Prospective memory, function (
311554006) -
Provision of memory device (
713112001) -
Psychologic test, Wechsler memory scale (
80982006) -
Recent memory, function (
69063000) -
Recognition memory test (
273740006) -
Recognition, function (
312020002) -
Recovery of memory (
225443005) -
Referral to memory assessment service (
823961000000102) -
Referral to memory clinic (
415276009) -
Referral to memory clinic (
170231000000104) -
Referral to memory clinic (
174891000000105) -
Referral to memory clinic declined (
868751000000100) -
Referral to memory clinic declined (
868761000000102) -
Reliving traumatic memories (
285216009) -
Remote memory, function (
81964002) -
Resident tissue macrophage (
14295007) -
Response to memory test for address recall (
165306006) -
Response to memory test for counting down (
165303003) -
Response to memory test for important event (
165297005) -
Response to memory test for important person (
165300000) -
Response to memory test for months of year in reverse (
1034871000000101) -
Response to memory test for own age (
165279002) -
Response to memory test for own date of birth (
165291006) -
Response to memory test for present month (
165294003) -
Response to memory test for present place (
165285009) -
Response to memory test for present time (
165282007) -
Response to memory test for present year (
165288006) -
Retrograde amnesia (
51921000) -
Retrospective falsification (
26581009) -
Rivermead Behavioral Memory Test - Third Edition (
982571000000107) -
Rivermead Behavioral Memory Test - Third Edition score (
982591000000106) -
Rivermead Behavioral Memory Test Third Edition (
718088009) -
Rivermead Behavioral Memory Test Third Edition score (
718692001) -
Rivermead Behavioral Memory Test adult version score (
718693006) -
Rivermead Behavioral Memory Test for Children score (
718694000) -
Rivermead Behavioural Memory Test - adult version score (
1048651000000100) -
Rivermead Behavioural Memory Test for Children score (
1048671000000109) -
Rivermead behavioral memory test (
273761004) -
Rivermead behavioral memory test - adult version (
307801002) -
Rivermead behavioral memory test - child version (
307802009) -
Rivermead behavioral memory test score (
446518001) -
Rivermead behavioural memory test score (
748621000000108) -
Route recognition, function (
312021003) -
Sea-blue histiocyte (
39474009) -
Secretory macrophage (
35113007) -
Seen in memory clinic (
432806004) -
Seen in memory clinic (
309801000000104) -
Seen in memory clinic (
309811000000102) -
Seen in memory clinic (
309821000000108) -
Semantic memory (
283994001) -
Semantic memory performance (
283890009) -
Sharpened memory for remote events (
247605007) -
Short Orientation - Memory - Concentration Test (
273803007) -
Short Orientation - Memory - Concentration Test score (
1255876008) -
Short orientation-memory-concentration test - alternative version (
273804001) -
Short-term memory performance (
247589005) -
Short-term memory test (
273805000) -
Short-term memory within normal limits (
247590001) -
Stroke Impact Scale version 3.0 memory score (
880231000000100) -
Stroke impact scale version 3.0 memory score (
707521001) -
Suppressor cell (
50146007) -
T helper subset 1 cell (
418698006) -
T helper subset 2 cell (
418340005) -
T lymphocyte (
57184004) -
T lymphocyte positive for CD16 antigen and CD57 antigen (
115416000) -
T lymphocyte positive for CD16 antigen and negative for CD57 antigen (
115415001) -
T lymphocyte positive for CD4 antigen (
115412003) -
T lymphocyte positive for both CD3 antigen and CD4 antigen (
115396002) -
T lymphocyte positive for both CD4 antigen and CD25 antigen (
115399009) -
T lymphocyte positive for both CD4 antigen and CD29 antigen (
115401003) -
T lymphocyte positive for both CD4 antigen and CD45RA antigen (
115403000) -
T lymphocyte positive for both CD4 antigen and human leukocyte antigen DR (
115405007) -
T lymphocyte positive for both CD8 antigen and CD11a antigen (
115413008) -
T lymphocyte positive for both CD8 antigen and CD11b antigen (
115414002) -
TYM (Test Your Memory) test (
896201000000107) -
Tactile memory (
283923002) -
Talks about the past (
225041002) -
Temporary loss of memory (
162200009) -
Test Your Memory test (
896191000000105) -
Test Your Memory test total score (
1084821000000107) -
Test Your Memory test total score (
763123000) -
Tissue eosinophil (
55109005) -
Tissue neutrophil (
88397004) -
Topographical memory (
283925009) -
Transient epileptic amnesia (
395689002) -
Transient global amnesia (
230736007) -
Transient memory loss (
307413004) -
Unable to recall five digit number at five minutes (
285212006) -
Unable to recall random address at five minutes (
285208000) -
Unable to remember current year (
285197006) -
Unable to remember day of the week (
285191007) -
Unable to remember faces (
285228001) -
Unable to remember month of year (
285194004) -
Unable to remember motor skills (
285219002) -
Unable to remember name of current prime minister (
247610006) -
Unable to remember name of reigning monarch (
247609001) -
Unable to remember new motor skills (
285221007) -
Unable to remember objects (
285225003) -
Unable to remember old motor skills (
285223005) -
Unable to remember own age (
247613008) -
Unable to remember own date of birth (
285188007) -
Unable to remember past events (
1075681000000104) -
Unable to remember people (
1075691000000102) -
Unable to remember places (
1075701000000102) -
Unable to remember routines (
1075711000000100) -
Unable to remember sounds (
285230004) -
Unable to remember today's date (
247608009) -
Unable to reproduce geometric figure at five minutes (
285210003) -
Uncompensated short term memory deficit (
33254005) -
Unpleasant memories (
225034008) -
Use of memory retrieval aids (
283993007) -
Valentine auditory memory test (
273888001) -
Veiled cell (
127942009) -
Verbal memory encoding (
311529006) -
Verbal memory for events (
283995000) -
Verbal memory for names (
283933005) -
Verbal memory for objects (
283934004) -
Verbal memory observable (
283914000) -
Verbal memory recall (
311531002) -
Verbal memory storage (
311530001) -
Verbal short-term memory performance (
283885006) -
Visual memory (
283917007) -
Visual memory for faces (
283931007) -
Visual memory for objects (
283932000) -
Visual short-term memory performance (
283888008) -
Wechsler memory scale (
273921009) -
Wechsler memory scale revised (
311481008) -
Wepman digit span test (
273924001) -
Williams memory assessment scales (
311480009) -
[D]Amnesia (retrograde) (
206784007) -
[D]Amnesia (retrograde) (
495901000000102)