Spastic Paraplegia 5a, Autosomal Recessive MeSH Supplementary Concept Data 2024

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Concepts

MeSH Supplementary: Spastic Paraplegia 5a, Autosomal Recessive
Unique ID: C564811
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564811
Registry Number: 0
Heading Mapped to: *Spastic Paraplegia, Hereditary
Frequency: 2
Note: also known as SPG5a; associated with mutation in the CYP7B1gene
Date of Entry: 2012/08/24

Spastic Paraplegia 5a, Autosomal Recessive Preferred

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