OMOP Concept 37470696
Genetic intellectual disability
StandardConditionSNOMED1362108000Disorder
Maps from
1
Descendants
538
Valid from
1 Apr 2025
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Genetic intellectual disability via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| ICD10CM | F78.A | Other genetic related intellectual disabilities | Non-standard |
Synonyms
Alternative names recorded for Genetic intellectual disability across source vocabularies.
- discapacidad intelectual de causa genética
- discapacidad intelectual de causa genética (trastorno)
- Genetic intellectual disability (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(14)Roll up to these when you need a wider cohort.
- 1Genetic disease
- 1Intellectual disability
- 2Abnormal behavior
- 2Disease
- 2Impaired cognition
- 2Intellectual ability - finding
- 2Neurodevelopmental disorder
- 3Behavior finding
- 3Clinical finding
- 3Cognitive function finding
- 3Developmental disorder
- 3Intelligence finding
- 4Functional finding
- 4Mental state, behavior and/or psychosocial function finding
Narrower concepts
(538)Included automatically when you query with descendants.
- 111p15.4 microduplication syndrome
- 114q24.1q24.3 microdeletion syndrome
- 117q11.2 microduplication syndrome
- 117q24.2 microdeletion syndrome
- 119p13.3 microduplication syndrome
- 120q11.2 microdeletion syndrome
- 121q22.11q22.12 microdeletion syndrome
- 12p13.2 microdeletion syndrome
- 12p21 microdeletion syndrome without cystinuria
- 13-methylglutaconic aciduria type 9
- 14q25 proximal deletion syndrome
- 15-amino-4-imidazole carboxamide ribosiduria
- 15p13 microduplication syndrome
- 18q24.3 microdeletion syndrome
- 19q21.13 microdeletion syndrome
- 19q31.1q31.3 microdeletion syndrome
- 19q33.3q34.11 microdeletion syndrome
- 1Achalasia microcephaly syndrome
- 1ADNP-related multiple congenital anomalies, intellectual disability, autism spectrum disorder
- 1Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome
- 1Agenesis of corpus callosum and abnormal genitalia syndrome
- 1Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome
- 1Agenesis of corpus callosum, macrocephaly, hypertelorism syndrome
- 1AHDC1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome
- 1Allan-Herndon-Dudley syndrome
Showing 25 of 538. Retrieve the full set via the API.
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