OMOP Concept 43530633
Congenital hypoplasia of brain
StandardConditionSNOMED127551000119100Disorder
Maps from
1
Descendants
64
Valid from
31 Jul 2013
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Congenital hypoplasia of brain via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 127551000119100 | Congenital hypoplasia of brain | Non-standard |
Synonyms
Alternative names recorded for Congenital hypoplasia of brain across source vocabularies.
- Congenital hypoplasia of brain (disorder)
- hipoplasia congénita de cerebro
- hipoplasia congénita de cerebro (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(18)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of brain
- 2Congenital anomaly of central nervous system
- 2Congenital anomaly of head
- 2Disorder of brain
- 3Congenital anomaly of nervous system
- 3Congenital malformation
- 3Disorder of head
- 3Disorder of the central nervous system
- 3Finding of brain
- 4Central nervous system finding
- 4Congenital disease
- 4Developmental disorder
- 4Disease
- 4Disorder of nervous system
- 4Head finding
- 5Clinical finding
- 5Disorder of body system
- 5Disorder of fetus and/or newborn
Narrower concepts
(64)Included automatically when you query with descendants.
- 1Congenital hypoplasia of part of brain
- 1Microcephalus, brain defect, spasticity, hypernatremia syndrome
- 2Congenital cerebellar hypoplasia
- 2Congenital hypoplasia of cerebrum
- 2Hypoplasia of brain gyri
- 3Cerebellar-facial-dental syndrome
- 3Congenital cerebellar ataxia due to RNU12 mutation
- 3Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration
- 3Congenital hypoplasia of inner granular layer of cerebellum
- 3Congenital muscular dystrophy with cerebellar involvement
- 3Congenital pontocerebellar hypoplasia
- 3Dandy-Walker syndrome
- 3Endosteal hyperostoses with cerebellar hypoplasia
- 3Granular cell hypoplasia
- 3Hypoplasia of corpus callosum
- 3Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome
- 3Isolated bilateral hemispheric cerebellar hypoplasia
- 3Isolated cerebellar vermis hypoplasia
- 3Isolated unilateral hemispheric cerebellar hypoplasia
- 3Lethal brain and heart developmental defects syndrome
- 3Lissencephaly with cerebellar hypoplasia
- 3Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome
- 3Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome
- 3Porencephaly, cerebellar hypoplasia, internal malformations syndrome
- 3Septo-optic dysplasia sequence
- 3Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome
- 3Short stature, pituitary and cerebellar defect and small sella turcica syndrome
- 3White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome
- 3X-linked cerebral, cerebellar, coloboma syndrome
- 3X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome
- 3X-linked intellectual disability with cerebellar hypoplasia syndrome
- 4Aase Smith type 1 syndrome
- 4Congenital pontocerebellar hypoplasia type 1
- 4Congenital pontocerebellar hypoplasia type 10
- 4Congenital pontocerebellar hypoplasia type 11
- 4Congenital pontocerebellar hypoplasia type 12
- 4Congenital pontocerebellar hypoplasia type 13
- 4Congenital pontocerebellar hypoplasia type 14
- 4Congenital pontocerebellar hypoplasia type 2
- 4Congenital pontocerebellar hypoplasia type 3
- 4Congenital pontocerebellar hypoplasia type 4
- 4Congenital pontocerebellar hypoplasia type 5
- 4Congenital pontocerebellar hypoplasia type 6
- 4Congenital pontocerebellar hypoplasia type 7
- 4Congenital pontocerebellar hypoplasia type 8
- 4Congenital pontocerebellar hypoplasia type 9
- 4Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation
- 4Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome
- 4Dandy-Walker malformation with postaxial polydactyly syndrome
- 4Dandy-Walker syndrome with spina bifida
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