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Uniparental disomy

Uniparental disomy: Introduction

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

Symptoms of Uniparental disomy

Home Diagnostic Testing

Home medical testing related to Uniparental disomy:

Wrongly Diagnosed with Uniparental disomy?

Causes of Uniparental disomy

Read more about causes of Uniparental disomy.

Uniparental disomy: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Uniparental disomy

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Uniparental disomy: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Hospitals & Clinics: Uniparental disomy

Research quality ratings and patient safety measures for medical facilities in specialties related to Uniparental disomy:

Choosing the Best Hospital: More general information, not necessarily in relation to Uniparental disomy, on hospital performance and surgical care quality:

Evidence Based Medicine Research for Uniparental disomy

Medical research articles related to Uniparental disomy include:

Click here to find more evidence-based articles on the TRIP Database

Research about Uniparental disomy

Visit our research pages for current research about Uniparental disomy treatments.

Statistics for Uniparental disomy

Uniparental disomy: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Uniparental disomy, or answer someone else's question, on our message boards:

Definitions of Uniparental disomy:

Uniparental disomy 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, or a subtype of Uniparental disomy, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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

Related Uniparental disomy Info

Videos about Uniparental disomy

 

More information about Uniparental disomy

  1. Uniparental disomy: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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