MeSH Browser

MeSH Supplementary: Spinocerebellar ataxia, autosomal recessive 5
Unique ID: C537311
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537311
Entry Term(s): Cerebellar ataxia with mental retardation, optic atrophy, and skin abnormalities
Registry Numbers: 0
Heading Mapped to: *Spinocerebellar Degenerations
Frequency: 1
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Spinocerebellar ataxia, autosomal recessive 5 MeSH Supplementary Concept Data 2025