FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term prothrombin thrombophilia ID (Ontology) DOID:0080701 (Human Disease)
Definition 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.
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 Genes
 prothrombin thrombophilia      11
 for disease ribbon | prothrombin thrombophilia      11
 model of | prothrombin thrombophilia      11
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
blood coagulation disease       |
 |__thrombophilia_______________|
                                prothrombin thrombophilia  11 rec.
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Is a autosomal dominant disease
thrombophilia
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MIM:188050