Sensorimotor neuropathy with ataxia, autosomal dominant MeSH Supplementary Concept Data 2024

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MeSH Supplementary: Sensorimotor neuropathy with ataxia, autosomal dominant
Unique ID: C537197
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537197
Entry Term(s): Spinocerebellar ataxia 18
Heading Mapped to: *Spinocerebellar Degenerations
Frequency: 5
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Sensorimotor neuropathy with ataxia, autosomal dominant Preferred

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