OMOP Concept 37469347
Neurodevelopmental delay
StandardConditionSNOMED1137472008Disorder
Maps from
2
Descendants
124
Valid from
1 Aug 2025
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Neurodevelopmental delay via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| HPO | HP_0012758 | Neurodevelopmental delay | Non-standard |
| Read | Eu86.00 | [X]Neurodevelopmental delay | Non-standard |
Synonyms
Alternative names recorded for Neurodevelopmental delay across source vocabularies.
- Neurodevelopmental delay (disorder)
- retraso del neurodesarrollo
- retraso del neurodesarrollo (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(5)Roll up to these when you need a wider cohort.
Narrower concepts
(124)Included automatically when you query with descendants.
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- 1Autism spectrum disorder due to AUTS2 deficiency
- 1Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome
- 1Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency
- 1Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome
- 1Basel Vanagaite Smirin Yosef syndrome
- 1CAD-CDG - carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation
- 1CCNK-related neurodevelopmental disorder, severe intellectual disability, facial dysmorphism syndrome
- 1CDK13-related congenital heart defects, intellectual disability, facial dysmorphism syndrome
- 1CDKL5 developmental and epileptic encephalopathy
- 1CHD3-related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome
- 1CHD4-related neurodevelopmental disorder
- 1Clumsiness - motor delay
- 1Coffin-Lowry syndrome
- 1Combined oxidative phosphorylation defect type 39
- 1Congenital contracture of limbs and face, hypotonia, developmental delay syndrome
- 1Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome
- 1Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome
Showing 25 of 124. Retrieve the full set via the API.
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