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DO Term : autosomal dominant limb-girdle muscular dystrophy type 2 [DOID:0110304] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in heterozygous mutation in the TNPO3 gene on chromosome 7q32.
  • synonyms:
  • 608423,
  • autosomal dominant limb-girdle muscular dystrophy type 1F,
  • ICD10CM:G71.0,
  • LGMD1F,
  • OMIM:608423,
  • ORDO:55595,
  • muscular dystrophy limb-girdle type 1F
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