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Diseases » Uniparental disomy of 11 » Introduction
 

Uniparental disomy of 11

Uniparental disomy of 11: Introduction

Uniparental disomy of 11: A condition which is characterised by the uniparental disomy of chromosome 11. More detailed information about the symptoms, causes, and treatments of Uniparental disomy of 11 is available below.

Symptoms of Uniparental disomy of 11

See full list of 11 symptoms of Uniparental disomy of 11

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Disease Topics Related To Uniparental disomy of 11

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Medical Textbooks Online about Uniparental disomy of 11

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Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.

Wrongly Diagnosed with Uniparental disomy of 11?

Uniparental disomy of 11: Undiagnosed Conditions

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Misdiagnosis and Uniparental disomy of 11

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Uniparental disomy of 11: Research Doctors & Specialists

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Hospitals & Clinics: Uniparental disomy of 11

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Definitions of Uniparental disomy of 11:

Uniparental disomy of 11 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Uniparental disomy of 11, or a subtype of Uniparental disomy of 11, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)


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