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DO Term : autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 [DOID:0111520] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in the TWNK gene on chromosome 10q24.31.
  • synonyms:
  • PEOA3,
  • 609286,
  • autosomal dominant progressive external ophthalmoplegia 3,
  • OMIM:609286
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Ontology

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