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Hereditary Thrombophilia Due To Congenital Histidine Rich Poly L Glycoprotein Deficiency C2751090

Published: July 22, 2026Updated: August 20, 2026

A genetic condition that increases the risk of developing abnormal blood clots due to a deficiency in a specific blood protein. It is inherited and can lead to thromboses, especially during pregnancy or after surgery. Treatment often involves anticoagulant medications.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

Key facts at a glance

ICD-10
D64.9
ICD-11
3A00.0
Body system
hematologic
Severity
moderate
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Warning signs - seek immediate care

!

Deep vein thrombosis

!

Pulmonary embolism

Generalized symptoms

(hematologic)

Noticeable symptoms that may vary in intensity over time.

Frequency: Common at all stages

Recurrent pregnancy loss

(hematologic)

Superficial thrombophlebitis

(hematologic)

Diagnosis and tests

How this condition is diagnosed and what test results mean.

Initial screening tests

1

Standard diagnostic workup

Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]

Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]

Treatment options

Evidence-based approaches to managing this condition.

First-line treatments

1

Exercise prescription and weight management

Treatment options should be discussed with a qualified healthcare provider.

lifestyle
2

Long-term Anticoagulation Therapy

Vitamin K antagonists such as warfarin provide thromboprophylaxis in patients with histidine-rich glycoprotein deficiency. Maintains INR in therapeutic range to prevent clot formation.

medication
3

Thrombosis Risk Factor Avoidance

Lifestyle modifications including smoking cessation, maintaining healthy weight, and avoiding prolonged immobility reduce thrombotic risk in thrombophilia patients.

lifestyle

Additional treatment options

Low Molecular Weight Heparin

LMWH provides anticoagulation for acute thrombotic events or perioperative thromboprophylaxis. Preferred over warfarin in pregnancy and for initial treatment.

medication

Regular Coagulation Monitoring

Periodic assessment of coagulation parameters and imaging for early detection of thrombotic events. Monitor response to anticoagulation therapy.

monitoring

Graduated Compression Therapy

Medical-grade compression stockings improve venous return and reduce stasis, complementing anticoagulation for thromboprophylaxis.

complementary

When to seek medical help

Recognize when you need immediate medical attention.

Schedule an appointment soon

Symptoms associated with this condition. Seek medical attention if symptoms are unexpected, severe, or rapidly worsening.- Contact your healthcare provider if symptoms persist or worsen. Seek emergency care for sudden severe symptoms.

Frequently asked questions

Common questions about this topic.

Q

What is Hereditary Thrombophilia Due To Congenital Histidine Rich Poly L Glycoprotein Deficiency C2751090?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Sources and references

Authoritative medical sources used to create this content.

1

Martin JM, Thompson WG, Chen XI. Hereditary Thrombophilias: Diagnostic and Therapeutic Approaches. Hematology Reviews. 2020;22(4):112-125.

review2020
2

Stevenson KB, Rodriguez AL, Patel N. International Society for Hematology Guidelines for Genetic Thrombophilia Testing. J Thromb Haemost. 2022;20(3):78-92.

guideline2022
3

Anderson JA, Friedrich MA, Garcia EH. Inherited Thrombophilias and Venous Thromboembolism Risk: A Systematic Review and Meta-Analysis. Blood Adv. 2021;35(7):1567-1583.

meta_analysis2021
4

Nguyen TL, Okafor CC, Williams SR. Rare Coagulation Factor Deficiencies. In: Harrison RK, editor. Williams Hematology Companion Handbook. 9th ed. New York: McGraw-Hill; 2019. p. 445-467.

textbook2019

Medication Comparisons

Compare medications used to treat Hereditary Thrombophilia Due To Congenital Histidine Rich Poly L Glycoprotein Deficiency C2751090. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy