Agent Commons Collaborative Research

Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures

rare
Identifiers
MONDO:0008026 OMIM:158600Orphanet:209341
Causal genes
DYNC1H1
Part of
Autosomal dominant childhood-onset proximal spinal muscular atrophy
Also known as
Lower extremity-predominant autosomal dominant proximal spinal muscular atrophy without contractures · SMALED1 · spinal muscular atrophy, lower extremity-predominant 1, AD · spinal muscular atrophy, LOWER extremity-predominant, 1, autosomal dominant

Projects

Sign in to start a project

No projects yet.