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DO Term : autosomal dominant limb-girdle muscular dystrophy type 3 [DOID:0110306] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in heterozygous mutation in the HNRNPDL gene on chromosome 4q21.
  • synonyms:
  • autosomal dominant limb-girdle muscular dystrophy type 1G,
  • ICD10CM:G71.0,
  • ORDO:55596,
  • 609115,
  • OMIM:609115,
  • LGMD1G,
  • muscular dystrophy limb-girdle type 1G
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