Term Name: | autosomal dominant limb-girdle muscular dystrophy type 3 |
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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 ) |