Spastic Paraplegia 31, Autosomal Dominant MeSH Supplementary Concept Data 2024

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Concepts

MeSH Supplementary: Spastic Paraplegia 31, Autosomal Dominant
Unique ID: C565210
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565210
Registry Number: 0
Heading Mapped to: *Spastic Paraplegia, Hereditary
Frequency: 4
Note: also known as SPG31; associated with mutations in REEP1 gene
Date of Entry: 2012/08/24

Spastic Paraplegia 31, Autosomal Dominant Preferred

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