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Summary Literature (0)
DOID:9883 - Becker muscular dystrophy

Disease Ontology Definition:A muscular dystrophy that involves slowly worsening muscle weakness of the legs and pelvis, and has_material_basis_in X-linked recessive inheritance of mutation in the dystrophin gene on chromosome Xp21.

Synonyms: benign congenital myopathy, Benign pseudohypertrophic muscular dystrophy

Xenbase Genes : dmd.2, dmd.3, dmd

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010311 - Becker muscular dystrophy

MIM:
MIM:300376 - MUSCULAR DYSTROPHY, BECKER TYPE; BMD

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): muscular dystrophy (is_a)