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Familial myelofibrosis

Familial myelofibrosis: Introduction

Familial myelofibrosis: A rare condition where progressive scarring or fibrosis of the bone marrow impairs it's ability to make blood cells causing symptoms such as anemia and liver and spleen enlargement. More detailed information about the symptoms, causes, and treatments of Familial myelofibrosis is available below.

Symptoms of Familial myelofibrosis

Home Diagnostic Testing

Home medical testing related to Familial myelofibrosis:

Wrongly Diagnosed with Familial myelofibrosis?

Causes of Familial myelofibrosis

Read more about causes of Familial myelofibrosis.

Misdiagnosis and Familial myelofibrosis

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Familial myelofibrosis: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Familial myelofibrosis: Animations

Statistics for Familial myelofibrosis

Familial myelofibrosis: Broader Related Topics

User Interactive Forums

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Definitions of Familial myelofibrosis:

Familial myelofibrosis is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Familial myelofibrosis, or a subtype of Familial myelofibrosis, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Related Familial myelofibrosis Info

More information about Familial myelofibrosis

  1. Familial myelofibrosis: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing

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