Spinocerebellar ataxia type 22

Preferred Label : Spinocerebellar ataxia type 22;

ICD-11 definition : Spinocerebellar ataxia type 22 (SCA22) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by slowly progressive cerebellar ataxia and hyporeflexia.;

Details

Origin ID

1835077432;

UMLS CUI

C2746067;

Currated CISMeF NLP mapping
- Spinocerebellar ataxia 22 [MeSH concept]
- Spinocerebellar ataxia type 22 [ORDO Disease]
- spinocerebellar ataxia 22 [MeSH Supplementary Concept]
- spinocerebellar ataxia 22 [Disease (Nov.)]
See also inter- (CISMeF)
- Spinocerebellar ataxia 19 [OMIM Phenotype]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spinocerebellar ataxia 22 [MeSH concept]
- Spinocerebellar ataxia type 22 [ORDO Disease]
- spinocerebellar ataxia 22 [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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