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DO Term : autosomal dominant hyaline body myopathy [DOID:0111269] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hyaline body myopathy that has_material_basis_in heterozygous mutation in MYH7 on 14q11.2.
  • synonyms:
  • 608358,
  • Myopathy, myosin storage, autosomal dominant,
  • OMIM:608358,
  • MSMA,
  • congenital myopathy 7A,
  • myopathy with lysis of type I myofibrils
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Disease

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Ontology

Ontology Term --> All ancestors

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Ontology Term --> Direct parents





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