OMOP Concept 4099090
Dysgenesis of the cerebellum
StandardConditionSNOMED253171007Disorder
Maps from
4
Descendants
92
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
4 source codes normalize to Dysgenesis of the cerebellum via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 161055 | Malformation of the cerebellar folia | Non-standard |
| CIEL | 161588 | Cerebellar duplication | Non-standard |
| Nebraska Lexicon | 253171007 | Dysgenesis of the cerebellum | Non-standard |
| Read | P22Az00 | Anomaly of cerebellum NOS | Non-standard |
Synonyms
Alternative names recorded for Dysgenesis of the cerebellum across source vocabularies.
- disgenesia del cerebelo
- disgenesia del cerebelo (trastorno)
- Dysgenesis of the cerebellum (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(19)Roll up to these when you need a wider cohort.
- 1Cerebellar disorder
- 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
(92)Included automatically when you query with descendants.
- 1Anomalies of cerebellum
- 1Aplasia of cerebellum
- 1Aprosencephaly cerebellar dysgenesis
- 1Autosomal recessive cerebelloparenchymal disorder type 3
- 1Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome
- 1Cerebellar cortical dysplasia
- 1Chiari malformation
- 1Chudley McCullough syndrome
- 1Congenital abnormal shape of cerebellum
- 1Congenital cerebellar hypoplasia
- 1Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome
- 1Dentate dysplasia
- 1Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome
- 1Spinocerebellar ataxia dysmorphism syndrome
- 1Tubulinopathy-associated dysgyria
- 2Agenesis of cerebellum
- 2Agenesis of left hemisphere of cerebellum
- 2Agenesis of right hemisphere of cerebellum
- 2Aplasia of the vermis
- 2Cerebellar-facial-dental syndrome
- 2Chiari malformation type I
- 2Chiari malformation type II
- 2Chiari malformation type III
- 2Chiari malformation type IV
- 2Closed spina bifida with Arnold-Chiari malformation
- 2Congenital cerebellar ataxia due to RNU12 mutation
- 2Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration
- 2Congenital hypoplasia of inner granular layer of cerebellum
- 2Congenital muscular dystrophy with cerebellar involvement
- 2Congenital pontocerebellar hypoplasia
- 2Dandy-Walker syndrome
- 2Endosteal hyperostoses with cerebellar hypoplasia
- 2Granular cell hypoplasia
- 2Hemispheric cerebellar agenesis
- 2Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome
- 2Isolated cerebellar vermis hypoplasia
- 2Lethal brain and heart developmental defects syndrome
- 2Lissencephaly with cerebellar hypoplasia
- 2Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome
- 2Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome
- 2Porencephaly, cerebellar hypoplasia, internal malformations syndrome
- 2Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome
- 2White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome
- 2X-linked cerebral, cerebellar, coloboma syndrome
- 2X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome
- 2X-linked intellectual disability with cerebellar hypoplasia syndrome
- 3Aase Smith type 1 syndrome
- 3Arnold Chiari type 2 without hydrocephalus
- 3Capra DeMarco syndrome
- 3Cerebellum agenesis with hydrocephaly
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