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Disease Ontology Browser
Becker muscular dystrophy (DOID:9883)
Alliance: disease page
Synonyms: benign congenital myopathy; Benign pseudohypertrophic muscular dystrophy
Alt IDs: OMIM:300376, ORDO:98895, UMLS_CUI:C0699741
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.

Disease References using Mouse Models (1)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory