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DO Term : hereditary angioedema type III [DOID:0080940] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A hereditary angioedema that is characterized clinically by recurrent skin swelling, abdominal pain attacks, and potentially life-threatening upper airway obstruction and that has_material_basis_in heterozygous mutation in the gene encoding coagulation factor XII (F12) on chromosome 5q35.
  • synonyms:
  • 610618,
  • MESH:D056828,
  • OMIM:610618
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents