Autosomal dominant limb-girdle muscular dystrophy type 1H (LGMD1H) is a subtype of autosomal dominant limb-girdle muscular dystrophy characterized by slowly progressive proximal muscular weakness initially affecting the lower limbs (and later involving the upper limbs), hypotrophy of upper and lower limb-girdle muscles, hyporeflexia, calf hypertrophy, and increased serum creatine kinase. There is no involvement of oculo-facial-bulbar muscles and cardiac muscle. The disease is autosomal dominant limb-girdle muscular dystrophy type 1H (MONDO_0013297, a Monarch Disease Ontology id). Also known as: LGMD1H, muscular dystrophy limb-girdle type 1H.