MeSH Browser

MeSH Supplementary: Spinal Muscular Atrophy, Childhood, Proximal, Autosomal Dominant
Unique ID: C563560
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563560
Entry Term(s): Kugelberg-Welander Syndrome, Autosomal Dominant; Spinal Muscular Atrophy, Juvenile, Proximal, Autosomal Dominant
Registry Numbers: 0
Heading Mapped to: *Spinal Muscular Atrophies of Childhood
Frequency: 1
Note: mutation in DYNC1H1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Spinal Muscular Atrophy, Childhood, Proximal, Autosomal Dominant MeSH Supplementary Concept Data 2025