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DO Term : prothrombin thrombophilia [DOID:0080701] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A thrombophilia that is characterized by increases the risk of blood clots including deep vein thrombosis and pulmonary embolism and that has_material_basis_in heterozygous mutation in the thrombin gene (F2 gene) on chromosome 11p11.
  • synonyms:
  • OMIM:188050,
  • 188050
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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