Hereditary Cerebellar Ataxia

Preferred Label : Hereditary Cerebellar Ataxia;

NCIt related terms : Hereditary ataxia, unspecified;

NCIt definition : Cerebellar ataxia that is transmitted from parent to child.;

Codes from synonyms : G11.9;

Details

Origin ID

C140268;

UMLS CUI

C0270749;

Automatic exact mappings (from CISMeF team)
- Hereditary cerebellar ataxia [PASCAL descriptor]
- Marie's cerebellar ataxia (disorder) [SNOMED CT concept]
- marie's cerebellar ataxia [SNOMED Notion]
Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Marie's cerebellar ataxia (disorder) [SNOMED CT concept]
- marie cerebellar ataxia [MeSH concept]
- marie's cerebellar ataxia [SNOMED Notion]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- mCode Elixhauser Neurological Movement Disorder Value Set [NCIt concept]
- mCode Terminology [NCIt concept]
disease_has_primary_anatomic_site
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]

Keyword's position in hierarchy(ies) :

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