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scapuloperoneal spinal muscular atrophy, autosomal dominant

Disease Summary
Associated Targets (1)
Tchem

1


GARD Rare
Uniprot Description A clinically variable neuromuscular disorder characterized by neurogenic scapuloperoneal amyotrophy, laryngeal palsy, congenital absence of muscles, progressive scapuloperoneal atrophy and progressive distal weakness and amyotrophy.
Mondo Term and Equivalent IDs
MONDO:0008408:  scapuloperoneal spinal muscular atrophy, autosomal dominant
DOID:0111552: 
EFO:1001992: 
GARD:0010314: 
Orphanet:431255: 
SCTID:230248006: