OBO ID: DOID:9883
Term Name: Becker muscular dystrophy Search Ontology:
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
  • OMIM:300376
  • ORDO:98895
  • SNOMEDCT_US_2023_03_01:111501005
  • UMLS_CUI:C0699741
Ontology: Human Disease   ( DOID:9883 )
Relationships
is a type of:
OTHER Becker muscular dystrophy PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DMD Becker muscular dystrophy 300376
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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