Spastic paraplegia 29, autosomal dominant MeSH Supplementary Concept Data 2025

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Concepts

MeSH Supplementary: Spastic paraplegia 29, autosomal dominant
Unique ID: C536863
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536863
Registry Numbers: 0
Heading Mapped to: *Spastic Paraplegia, Hereditary
Frequency: 0
Note: Spg29 not included
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Spastic paraplegia 29, autosomal dominant Preferred

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