Olivopontocerebellar atrophy V

Preferred Label : Olivopontocerebellar atrophy V;

Obsolete resource : true;

Moved to : 607136;

Symbol : OPCA V;

CISMeF acronym : OPCA V;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Opca with dementia and extrapyramidal signs;

Inheritance : Autosomal dominant;

Prefixed ID : 164700;

Details

Origin ID

164700;

UMLS CUI

C1833995;

Currated CISMeF NLP mapping
- olivopontocerebellar atrophy V [MeSH concept]
- olivopontocerebellar atrophy V [MeSH Supplementary Concept]
HPO term(s)
- Neuronal loss [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- olivopontocerebellar atrophy V [MeSH Supplementary Concept]
- olivopontocerebellar atrophy V [MeSH concept]
Validated automatic mappings to NTBT
- Olivopontocerebellar Atrophy [NCIt concept]
- olivopontocerebellar atrophies [MeSH Descriptor]
- spinocerebellar ataxias [MeSH Descriptor]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients