About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory