autosomal dominant limb-girdle muscular dystrophy type 1H

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Summary

Literature (0)

DOID:0110303 - autosomal dominant limb-girdle muscular dystrophy type 1H

Disease Ontology Definition:An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in with variation in the region 3p25.1-p23.

Synonyms: LGMD1H, muscular dystrophy limb-girdle type 1H,

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant limb-girdle muscular dystrophy (is_a)