Term Name: autosomal dominant limb-girdle muscular dystrophy type 3
Synonyms: autosomal dominant limb-girdle muscular dystrophy type 1G, LGMD1G, muscular dystrophy limb-girdle type 1G
Definition: An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in heterozygous mutation in the HNRNPDL gene on chromosome 4q21.
Ontology: Human Disease [DOID:0110306]   ( DOID:0110306 )

Relationships
is a type of: autosomal dominant limb-girdle muscular dystrophy