Search Ontology:
Human Disease

prothrombin thrombophilia

Term ID
DOID:0080701
Synonyms
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. https://pubmed.ncbi.nlm.nih.gov/21707594/
References
Ontology
Human Disease   ( DOID:0080701 )
Relationships
is a type of
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Genes Involved
Zebrafish Models