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What is Thrombomodulin anomalies, familial?

What is Thrombomodulin anomalies, familial?

  • Thrombomodulin anomalies, familial: A defect in a protein involved with anticoagulation which results in an increased risk of developing blood clots which can result in death.

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Thrombomodulin anomalies, familial as a "rare disease".
Source - Orphanet

Thrombomodulin anomalies, familial: Introduction

Types of Thrombomodulin anomalies, familial:

Broader types of Thrombomodulin anomalies, familial:

How serious is Thrombomodulin anomalies, familial?

Complications of Thrombomodulin anomalies, familial: see complications of Thrombomodulin anomalies, familial

What causes Thrombomodulin anomalies, familial?

Causes of Thrombomodulin anomalies, familial: see causes of Thrombomodulin anomalies, familial

What are the symptoms of Thrombomodulin anomalies, familial?

Symptoms of Thrombomodulin anomalies, familial: see symptoms of Thrombomodulin anomalies, familial

Complications of Thrombomodulin anomalies, familial: see complications of Thrombomodulin anomalies, familial

Thrombomodulin anomalies, familial: Testing

Diagnostic testing: see tests for Thrombomodulin anomalies, familial.

Misdiagnosis: see misdiagnosis and Thrombomodulin anomalies, familial.

How is it treated?

Doctors and Medical Specialists for Thrombomodulin anomalies, familial: Hematologist ; see also doctors and medical specialists for Thrombomodulin anomalies, familial.
Treatments for Thrombomodulin anomalies, familial: see treatments for Thrombomodulin anomalies, familial

Name of Thrombomodulin anomalies, familial

Main name of condition: Thrombomodulin anomalies, familial

 

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