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DO Term : Becker muscular dystrophy [DOID:9883] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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,
  • UMLS_CUI:C0699741,
  • benign congenital myopathy,
  • OMIM:300376,
  • GARD:5900,
  • ORDO:98895,
  • SNOMEDCT_US_2023_03_01:111501005,
  • 300376
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Disease

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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents