OMOP Concept 432898
Severe intellectual disability
StandardConditionSNOMED40700009Disorder
Maps from
37
Descendants
20
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
37 source codes normalize to Severe intellectual disability via the OMOP "Maps to" relationship.
Showing 25 of 37 source codes. Retrieve the full set via the API.
Synonyms
Alternative names recorded for Severe intellectual disability across source vocabularies.
- retraso mental severo
- retraso mental severo (C.I. 20 - 34)
- retraso mental severo (trastorno)
- Severe intellectual development disorder
- Severe intellectual disability (disorder)
- Severe learning disability
- Severe learning disability, intelligence quotient in range 20-34
- Severe learning impairment, intelligence quotient in range 20-34
- Severe mental retardation (Intelligence Quotient 20-34)
- Severe mental retardation (I.Q. 20-34)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(13)Roll up to these when you need a wider cohort.
- 1Intellectual disability
- 2Abnormal behavior
- 2Impaired cognition
- 2Intellectual ability - finding
- 2Neurodevelopmental disorder
- 3Behavior finding
- 3Cognitive function finding
- 3Developmental disorder
- 3Intelligence finding
- 4Disease
- 4Functional finding
- 4Mental state, behavior and/or psychosocial function finding
- 5Clinical finding
Narrower concepts
(20)Included automatically when you query with descendants.
- 13-methylglutaconic aciduria type 9
- 1Anterior maxillary protrusion, strabismus, intellectual disability syndrome
- 1CCNK-related neurodevelopmental disorder, severe intellectual disability, facial dysmorphism syndrome
- 1Congenital insensitivity to pain with severe intellectual disability
- 1Congenital pontocerebellar hypoplasia type 14
- 1Craniosynostosis, microretrognathia, severe intellectual disability syndrome
- 1Fatty acyl-CoA reductase 1 deficiency
- 1Fryns Smeets Thiry syndrome
- 1Intellectual disability, early-onset cataract, microcephaly syndrome
- 1Keppen Lubinsky syndrome
- 1Microphthalmia with brain atrophy syndrome
- 1Neurodevelopmental delay, intellectual disability, ataxia, feeding difficulty syndrome
- 1NRXN1-related severe neurodevelopmental disorder, motor stereotypies, chronic constipation, sleep-wake cycle disturbance
- 1Posterior-predominant lissencephaly, broad flat pons and medulla-midline crossing defects syndrome
- 1Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome
- 1Severe intellectual disability and progressive spastic paraplegia
- 1Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome
- 1Severe intellectual disability, progressive postnatal microcephaly, midline stereotypic hand movements syndrome
- 1Severe intellectual disability, progressive spastic diplegia syndrome
- 1X-linked intellectual disability, limb spasticity, retinal dystrophy, arginine vasopressin deficiency
Get this concept via the API
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