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Thrombomodulin anomalies, familial

Thrombomodulin anomalies, familial: Introduction

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. More detailed information about the symptoms, causes, and treatments of Thrombomodulin anomalies, familial is available below.

Symptoms of Thrombomodulin anomalies, familial

Home Diagnostic Testing

Home medical testing related to Thrombomodulin anomalies, familial:

Wrongly Diagnosed with Thrombomodulin anomalies, familial?

Thrombomodulin anomalies, familial: Complications

Review possible medical complications related to Thrombomodulin anomalies, familial:

Causes of Thrombomodulin anomalies, familial

Read more about causes of Thrombomodulin anomalies, familial.

Misdiagnosis and Thrombomodulin anomalies, familial

Unnecessary hysterectomies due to undiagnosed bleeding disorder in women: The bleeding disorder called Von Willebrand's disease is quite...read more »

Thrombomodulin anomalies, familial: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Thrombomodulin anomalies, familial: Animations

Statistics for Thrombomodulin anomalies, familial

Thrombomodulin anomalies, familial: Broader Related Topics

User Interactive Forums

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Definitions of Thrombomodulin anomalies, familial:

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

Related Thrombomodulin anomalies, familial Info

More information about Thrombomodulin anomalies, familial

  1. Thrombomodulin anomalies, familial: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Complications
 

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