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DOID:0110306 - autosomal dominant limb-girdle muscular dystrophy type 3
Disease Ontology Definition:An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in heterozygous mutation in the HNRNPDL gene on chromosome 4q21.
Synonyms: autosomal dominant limb-girdle muscular dystrophy type 1G, LGMD1G, muscular dystrophy limb-girdle type 1G
Xenbase Genes : hnrnpdl
MONDO:0012193 - autosomal dominant limb-girdle muscular dystrophy type 1G |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee