Spastic paraplegia 19, autosomal dominant MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Spastic paraplegia 19, autosomal dominant
Unique ID: C536856
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536856
Registry Numbers: 0
Heading Mapped to: *Spastic Paraplegia, Hereditary
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Spastic paraplegia 19, autosomal dominant Preferred

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