MeSH Browser

MeSH Supplementary: Spastic paraplegia 6, autosomal dominant
Unique ID: C536866
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536866
Entry Term(s): Familial Spastic Paraplegia, Autosomal Dominant, 3; Familial spastic paraplegia, autosomal dominant 3; Fsp3; Spg6
Heading Mapped to: *Spastic Paraplegia, Hereditary
Frequency: 4
Note: Fsp3; Spg6 not included
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Spastic paraplegia 6, autosomal dominant MeSH Supplementary Concept Data 2024