ataxia, sensory, autosomal dominant

Preferred Label : ataxia, sensory, autosomal dominant;

MeSH note : mutation in RNF170;

Origin ID

C563818;

UMLS CUI

C1837015;

Automatic exact mappings (from CISMeF team)
- Ataxia, sensory, 1, autosomal dominant [OMIM Phenotype]
MeSH term(s) associated for indexing
- ataxia [MeSH Descriptor]
Record concept(s)
- ataxia, sensory, autosomal dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ataxia, sensory, 1, autosomal dominant [OMIM Phenotype]