prothrombin gene mutation

Pathology

• p G20210A mutation associated with coagulopathy
• factor II deficiency if the mutation renders prothrombin non-functional

More general terms

• genetic disease of the blood/bone marrow

Additional terms

• prothrombin gene
• prothrombin genotyping
• prothrombin; coagulation factor II; contains: activation peptide fragment 1; activation peptide fragment 2; thrombin light chain; thrombin heavy chain (F2)

Component of

• thrombophilia (hypercoagulability) molecular diagnostic panel