Spinocerebellar ataxia type 25

Preferred Label : Spinocerebellar ataxia type 25;

ICD-11 definition : Spinocerebellar ataxia type 25 (SCA25) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by cerebellar ataxia and prominent sensory neuropathy.;

Details

Origin ID

8347192;

UMLS CUI

C1837518;

Currated CISMeF NLP mapping
- Spinocerebellar ataxia 25 [OMIM Phenotype]
- Spinocerebellar ataxia 25 [MeSH concept]
- Spinocerebellar ataxia type 25 [ORDO Disease]
- Spinocerebellar ataxia type 25 (disorder) [SNOMED CT concept]
- spinocerebellar ataxia 25 [MeSH Supplementary Concept]
- spinocerebellar ataxia 25 [Disease (Nov.)]
- spinocerebellar ataxia type 25 [DO Concept]
See also inter- (CISMeF)
- spinocerebellar ataxia 25 [ORDO Gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spinocerebellar ataxia 25 [OMIM Phenotype]
- Spinocerebellar ataxia 25 [MeSH concept]
- Spinocerebellar ataxia type 25 [ORDO Disease]
- Spinocerebellar ataxia type 25 (disorder) [SNOMED CT concept]
- spinocerebellar ataxia 25 [MeSH Supplementary Concept]
- spinocerebellar ataxia 25 [Disease (Nov.)]
- spinocerebellar ataxia 25 [ORDO Gene]
- spinocerebellar ataxia type 25 [DO Concept]

Keyword's position in hierarchy(ies) :

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