OMOP Concept 436077
Developmental delay
StandardConditionSNOMED248290002Disorder
Maps from
6
Descendants
212
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
6 source codes normalize to Developmental delay via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 119491 | Lack of Expected Normal Physiological Development in Childhood | Non-standard |
| CIEL | 119492 | Developmental delay | Non-standard |
| ICD9CM | 315 | Specific delays in development | Non-standard |
| ICD9CM | 315.8 | Other specified delays in development | Non-standard |
| ICD9CM | 315.9 | Unspecified delay in development | Non-standard |
| Read | R034E00 | [D]Developmental delay | Non-standard |
Synonyms
Alternative names recorded for Developmental delay across source vocabularies.
- Developmental delay (disorder)
- retraso congénito
- retraso congénito (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(3)Roll up to these when you need a wider cohort.
Narrower concepts
(212)Included automatically when you query with descendants.
- 11p35.2 microdeletion syndrome
- 12p21 microdeletion syndrome
- 1Behr syndrome
- 1Beta-D-mannosidosis
- 1Bohring Opitz syndrome
- 1Cardiocranial syndrome Pfeiffer type
- 1Cognitive developmental delay
- 1Congenital cataract, hearing loss, severe developmental delay syndrome
- 1Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome
- 1Congenital ichthyosis, microcephalus, tetraplegia syndrome
- 1Delayed pre-verbal development
- 1Delay in sexual development AND/OR puberty
- 1DEND syndrome
- 1Developmental delay, immunodeficiency, leukoencephalopathy, hypohomocysteinemia syndrome
- 1Developmental delay in feeding
- 1Developmental delay in social skills
- 1Distal 16p11.2 microdeletion syndrome
- 1Early-onset neurodegeneration, choreoathetoid movement, microcytic anemia due to IREB2 mutation
- 1Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome
- 1Expressive language delay
- 1Frank-Ter Haar syndrome
- 1Global developmental delay
- 1GNAO1-related developmental delay, seizures, movement disorder spectrum
- 1Intermediate DEND syndrome
- 1Joint contractures, developmental delay, Pierre Robin syndrome
Showing 25 of 212. Retrieve the full set via the API.
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