OBO ID: DOID:0080701
Term Name: prothrombin thrombophilia Search Ontology:
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:
OTHER prothrombin thrombophilia PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
F13A1 {Venous thrombosis, protection against} 188050
F2 Thrombophilia 1 due to thrombin defect 188050
HABP2 {Venous thromboembolism, susceptibility to} 188050
MTHFR {Thromboembolism, susceptibility to} 188050
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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