Ataxia, Spastic, 1, Autosomal Dominant MeSH Supplementary Concept Data 2024

Details
Concepts

MeSH Supplementary: Ataxia, Spastic, 1, Autosomal Dominant
Unique ID: C566993
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566993
Heading Mapped to: *Cerebellar Ataxia; *Spastic Paraplegia, Hereditary
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Ataxia, Spastic, 1, Autosomal Dominant Preferred

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