spinocerebellar ataxia 10

Preferred Label : spinocerebellar ataxia 10;

MeSH note : mutation in ATXN10;

CISMeF acronym : SCA10;

MeSH synonym : Sca10; SCA10 Spinocerebellar Ataxia 10;

Details

Origin ID

C566874;

UMLS CUI

C1963674;

Currated CISMeF NLP mapping
- Spinocerebellar ataxia 10 [OMIM Phenotype]
- Spinocerebellar ataxia type 10 [ICD-11 More detail]
- Spinocerebellar ataxia type 10 [ORDO Disease]
- Spinocerebellar ataxia type 10 (disorder) [SNOMED CT concept]
- spinocerebellar ataxia 10 [Disease (Nov.)]
- spinocerebellar ataxia type 10 [DO Concept]
MeSH term(s) associated for indexing
- DNA repeat expansion [MeSH Descriptor]
- spinocerebellar ataxias [MeSH Descriptor]
Record concept(s)
- spinocerebellar ataxia 10 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spinocerebellar ataxia 10 [OMIM Phenotype]
- Spinocerebellar ataxia type 10 [ORDO Disease]
- Spinocerebellar ataxia type 10 [ICD-11 More detail]
- Spinocerebellar ataxia type 10 (disorder) [SNOMED CT concept]
- spinocerebellar ataxia 10 [Disease (Nov.)]
- spinocerebellar ataxia type 10 [DO Concept]

Keyword's position in hierarchy(ies) :

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