Spinal Muscular Atrophy, Childhood, Proximal, Autosomal Dominant [Supplementary Concept]

mutation in DYNC1H1

Date introduced: November 5, 2012

MeSH Unique ID: C563560

Heading Mapped to:

• Spinal Muscular Atrophies of Childhood

Entry Terms:

• Kugelberg-Welander Syndrome, Autosomal Dominant
• Spinal Muscular Atrophy, Juvenile, Proximal, Autosomal Dominant