olivopontocerebellar atrophy II, autosomal recessive

Preferred Label : olivopontocerebellar atrophy II, autosomal recessive;

MeSH synonym : OPCA II, Fickler-Winkler type;

Origin ID

C564930;

UMLS CUI

C1850319;

Currated CISMeF NLP mapping
- Cerebellar ataxia and albinism [OMIM Phenotype]
MeSH term(s) associated for indexing
- olivopontocerebellar atrophies [MeSH Descriptor]
Record concept(s)
- olivopontocerebellar atrophy II, autosomal recessive [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cerebellar ataxia and albinism [OMIM Phenotype]