Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 3 (LGMDD3)

Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 3, also known as autosomal dominant limb-girdle muscular dystrophy type 1g, is related to myopathy, myofibrillar, 3 and muscular dystrophy, limb-girdle, autosomal dominant 1. An important gene associated with Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 3 is HNRNPDL (Heterogeneous Nuclear Ribonucleoprotein D Like), and among its related pathways/superpathways are Acute viral myocarditis and 13q12.12 copy number variation. Affiliated tissues include skeletal muscle, and related phenotypes are cataract and myopathy