OMOP Concept 37165055
Aprosencephaly cerebellar dysgenesis
StandardConditionSNOMED1237366005Disorder
Maps from
1
Descendants
0
Valid from
30 Sept 2022
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Aprosencephaly cerebellar dysgenesis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C563331 | Aprosencephaly and Cerebellar Dysgenesis | Non-standard |
Synonyms
Alternative names recorded for Aprosencephaly cerebellar dysgenesis across source vocabularies.
- aprosencefalia y disgenesia cerebelosa
- aprosencefalia y disgenesia cerebelosa (trastorno)
- Aprosencephaly cerebellar dysgenesis (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(33)Roll up to these when you need a wider cohort.
- 1Aprosencephaly
- 1Congenital malformation of cerebellum
- 1Disorder of midbrain
- 1Dysgenesis of the brainstem
- 1Genetic disease
- 1Hemicephaly
- 2Aprosencephaly/atelencephaly spectrum
- 2Cerebellar disorder
- 2Congenital absence of part of brain
- 2Congenital anomaly of brain
- 2Congenital anomaly of cerebrum
- 2Disease
- 2Disorder of brain stem
- 2Structural abnormality of brainstem
- 3Abnormality of neurogenesis
- 3Anencephalus
- 3Clinical finding
- 3Congenital anomaly of central nervous system
- 3Congenital anomaly of head
- 3Disorder of brain
- 4Amyelencephalus
- 4Congenital anomaly of nervous system
- 4Congenital malformation
- 4Disorder of head
- 4Disorder of the central nervous system
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