Spastic Paraplegia 42, Autosomal Dominant MeSH Supplementary Concept Data 2024

Details
Concepts

MeSH Supplementary: Spastic Paraplegia 42, Autosomal Dominant
Unique ID: C567262
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567262
Registry Numbers: 0
Heading Mapped to: *Spastic Paraplegia, Hereditary
Frequency: 1
Note: also known as SPG42
Date of Entry: 2012/08/24
Revision Date: 1955/01/01

Spastic Paraplegia 42, Autosomal Dominant Preferred

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