Search Ontology:
Human Disease

Becker muscular dystrophy

Term ID
DOID:9883
Synonyms
  • benign congenital myopathy
  • Benign pseudohypertrophic muscular dystrophy
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)
References
  • GARD:5900
  • MIM:300376
  • ORDO:98895
  • SNOMEDCT_US_2023_03_01:111501005
  • UMLS_CUI:C0699741
Ontology
Human Disease   ( DOID:9883 )
Relationships
is a type of
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Genes Involved
Zebrafish Models