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Spinocerebellar Ataxia, Autosomal Recessive 2 MeSH Supplementary Concept Data 2022


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 Preferred
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