OMOP Concept 762772
Hereditary cerebellar atrophy
StandardConditionSNOMED431641000124107Disorder
Maps from
1
Descendants
10
Valid from
1 Sept 2012
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Hereditary cerebellar atrophy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 431641000124107 | Hereditary cerebellar atrophy | Non-standard |
Synonyms
Alternative names recorded for Hereditary cerebellar atrophy across source vocabularies.
- Hereditary cerebellar atrophy (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(21)Roll up to these when you need a wider cohort.
- 1Hereditary cerebellar degeneration
- 2Cerebellar degeneration
- 2Hereditary degenerative disease of central nervous system
- 3Cerebellar disorder
- 3Degenerative brain disorder
- 3Degenerative disease of the central nervous system
- 3Hereditary disorder of nervous system
- 4Degenerative disorder
- 4Disorder of brain
- 4Disorder of nervous system
- 4Disorder of the central nervous system
- 4Hereditary disorder by system
- 5Central nervous system finding
- 5Disease
- 5Disorder of body system
- 5Disorder of head
- 5Finding of brain
- 5Hereditary disease
- 6Clinical finding
- 6Genetic disease
- 6Head finding
Narrower concepts
(10)Included automatically when you query with descendants.
- 1Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency
- 1Combined oxidative phosphorylation defect type 29
- 1Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome
- 1Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome
- 1Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum
- 1Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
- 1Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome
- 1Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome
- 1Progressive cerebello-cerebral atrophy
- 1Spinocerebellar ataxia type 45
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