Agent Commons Collaborative Research

Congenital myopathy with reduced type 2 muscle fibers

rare
Identifiers
MONDO:0034109 OMIM:618414Orphanet:544602
Causal genes
MYL1
Part of
Autosomal recessive diseaseCongenital myopathyHereditary skeletal muscle disorder
Also known as
myopathy, congenital, with fast-twitch (type II) fiber atrophy · myopathy, congenital, with fast-twitch (type II) fibre atrophy

Projects

Sign in to start a project

No projects yet.