OMOP Concept 4293897
Hereditary cerebellar degeneration
StandardConditionSNOMED37650008Disorder
Maps from
2
Descendants
83
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Source codes that map to this concept
2 source codes normalize to Hereditary cerebellar degeneration via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 117589 | Hereditary Spinocerebellar Degeneration | Non-standard |
| CIEL | 117590 | Hereditary Cerebellar Degeneration | Non-standard |
Synonyms
Alternative names recorded for Hereditary cerebellar degeneration across source vocabularies.
- degeneración cerebelosa hereditaria
- degeneración cerebelosa hereditaria (trastorno)
- Hereditary cerebellar degeneration (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(20)Roll up to these when you need a wider cohort.
- 1Cerebellar degeneration
- 1Hereditary degenerative disease of central nervous system
- 2Cerebellar disorder
- 2Degenerative brain disorder
- 2Degenerative disease of the central nervous system
- 2Hereditary disorder of nervous system
- 3Degenerative disorder
- 3Disorder of brain
- 3Disorder of nervous system
- 3Disorder of the central nervous system
- 3Hereditary disorder by system
- 4Central nervous system finding
- 4Disease
- 4Disorder of body system
- 4Disorder of head
- 4Finding of brain
- 4Hereditary disease
- 5Clinical finding
- 5Genetic disease
- 5Head finding
Narrower concepts
(83)Included automatically when you query with descendants.
- 1Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome
- 1Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency
- 1Friedreich ataxia
- 1Hereditary cerebellar atrophy
- 1Infantile cerebellar and retinal degeneration
- 1Myoclonic epilepsy myopathy sensory ataxia
- 1Spinocerebellar ataxia
- 2Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome
- 2Adult-onset autosomal recessive cerebellar ataxia
- 2Amyotrophic lateral sclerosis with spinocerebellar ataxia
- 2ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis
- 2Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency
- 2Autosomal recessive cerebellar ataxia due to STUB1 deficiency
- 2Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUBCN deficiency
- 2Autosomal recessive cerebellar ataxia, psychomotor delay syndrome
- 2Autosomal recessive cerebelloparenchymal disorder type 3
- 2Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome
- 2Azorean disease
- 2Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia
- 2Combined oxidative phosphorylation defect type 29
- 2Corneal cerebellar syndrome
- 2Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome
- 2Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome
- 2Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome
- 2Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum
Showing 25 of 83. Retrieve the full set via the API.
Get this concept via the API
Resolve Hereditary cerebellar degeneration - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.
curl "https://api.omophub.com/v1/concepts/4293897?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card