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. [ http://purl.obolibrary.org/obo/ECO_0007636 http://purl.obolibrary.org/obo/ECO_0007645 ]

Synonyms: benign congenital myopathy Benign pseudohypertrophic muscular dystrophy

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS_CUI
  • ORDO
  • OMIM:300376
  • GARD
  • SNOMEDCT_US_2019_09_01
comment

OMIM mapping confirmed by DO. [SN].

has obo namespace

disease_ontology

id

DOID:9883

Term relations

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