Autosomal dominant limb-girdle muscular dystrophy type 1D (LGMD1D) is a limb girdle muscular dystrophy (LGMD ; see this term) characterized by muscular weakness, primarily affecting the pelvic and shoulder girdles with no bulbar weakness or dysarthria. The disease is Autosomal dominant limb-girdle muscular dystrophy type 1D (Orphanet rare-disease nomenclature term Orphanet_34516). Also known as: LGMD1D.