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DO Term : long QT syndrome 11 [DOID:0110652] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the AKAP9 gene on chromosome 7q21.2.
  • synonyms:
  • GARD:10437,
  • ICD10CM:I45.8,
  • MESH:C567513,
  • OMIM:611820,
  • LQT11,
  • 611820
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Disease

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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents