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GTR Home > Tests > Genetic Study of Hereditary Thrombophilia (11 genes)


This is a clinical test intended for Help: Diagnosis, Mutation Confirmation, Risk Assessment, Screening, Therapeutic management

Clinical summary


An instance of thrombophilia that is inherited. [from MONDO]

Conditions tested

Target population


Individuals with personal or family history of thromboembolic diseases, pulmonary thromboembolism, stroke or myocardial infarction at young ages , Family history of thrombotic vascular diseases (TVD), No history of TVD but exposed to environmental risk factors (prolonged immobilization: long travels, orthopedic and major surgeries; muscle and vessels injuries, pregnancy and postpartum, chronic disease, age)


Not provided

Clinical validity


Not provided

Clinical utility


Establish or confirm diagnosis

Guidance for management

Practice guidelines

  • NICE, 2023
    UK NICE Guideline NG158, Venous thromboembolic diseases: diagnosis, management and thrombophilia testing, 2023

Consumer resources

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.