|OBO ID: DOID:9883|
|Term Name:||Becker muscular dystrophy||Search 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. (2)|
|Ontology:||Human Disease (DOID:9883)|
|is a type of:||
OTHER Becker muscular dystrophy PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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