Ataxia, Sensory, Autosomal Dominant MeSH Supplementary Concept Data 2024

Details
Concepts

MeSH Supplementary: Ataxia, Sensory, Autosomal Dominant
Unique ID: C563818
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563818
Registry Number: 0
Heading Mapped to: Ataxia / *congenital
Frequency: 2
Note: mutation in RNF170
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Ataxia, Sensory, Autosomal Dominant Preferred

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