Spinal Muscular Atrophy, Childhood, Proximal, Autosomal Dominant [Supplementary Concept]
mutation in DYNC1H1
Date introduced: November 5, 2012
MeSH Unique ID: C563560
Heading Mapped to:
Entry Terms:
- Kugelberg-Welander Syndrome, Autosomal Dominant
- Spinal Muscular Atrophy, Juvenile, Proximal, Autosomal Dominant