MeSH Browser

MeSH Supplementary: Spinocerebellar Ataxia, Autosomal Recessive 2
Unique ID: C565865
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565865
Entry Term(s): CPD III; CPD3; Cerebellar Granular Cell Hypoplasia and Mental Retardation, Congenital; Cerebellar Hypoplasia, Nonprogressive Norman Type; Cerebelloparenchymal Disorder III; SCAR2; Spinocerebellar Ataxia Autosomal Recessive 2
Registry Number: 0
Heading Mapped to: *Spinocerebellar Degenerations
Frequency: 2
Date of Entry: 2012/11/05
Revision Date: 2019/06/24

Spinocerebellar Ataxia, Autosomal Recessive 2 MeSH Supplementary Concept Data 2024