MeSH Browser

MeSH Supplementary: Spinocerebellar ataxia, autosomal recessive 10
Unique ID: C537309
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537309
Entry Term(s): Autosomal recessive spinocerebellar ataxia type 10; Spinocerebellar ataxia with blindness and deafness; Spinocerebellar ataxia, autosomal recessive 3; autosomal recessive spinocerebellar ataxia type 10 (SCAR10)
Registry Numbers: 0
Previous Indexing: Spinocerebellar Degenerations (2010-2025)
Heading Mapped to: Spinocerebellar Ataxias
Frequency: 1
Note: associated with mutations in ANO10 PROTEIN, HUMAN gene (OMIM: 613728).
Date of Entry: 2025/05/30
Revision Date: 2025/05/30

Spinocerebellar ataxia, autosomal recessive 10 MeSH Supplementary Concept Data 2025