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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 pseudohypertrophic muscular dystrophy, benign congenital myopathy
Xenbase Genes
:
dmd.2,
dmd,
dmd.1
| MONDO:0010311 - Becker muscular dystrophy |
| OMIM:300376 - MUSCULAR DYSTROPHY, BECKER TYPE; BMD |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
muscular dystrophy (is_a)