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What is Uniparental disomy of 11?

What is Uniparental disomy of 11?

  • Uniparental disomy of 11: A condition which is characterised by the uniparental disomy of chromosome 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)

Uniparental disomy of 11: Introduction

Types of Uniparental disomy of 11:

Broader types of Uniparental disomy of 11:

What causes Uniparental disomy of 11?

Causes of Uniparental disomy of 11: see causes of Uniparental disomy of 11

What are the symptoms of Uniparental disomy of 11?

Symptoms of Uniparental disomy of 11: see symptoms of Uniparental disomy of 11

Uniparental disomy of 11: Testing

Diagnostic testing: see tests for Uniparental disomy of 11.

Misdiagnosis: see misdiagnosis and Uniparental disomy of 11.

How is it treated?

Doctors and Medical Specialists for Uniparental disomy of 11: Medical Geneticist ; see also doctors and medical specialists for Uniparental disomy of 11.
Treatments for Uniparental disomy of 11: see treatments for Uniparental disomy of 11

Name and Aliases of Uniparental disomy of 11

Main name of condition: Uniparental disomy of 11

Other names or spellings for Uniparental disomy of 11:

Paternal uniparental disomy for chromosome 11 (type), Uniparental disomy of chromosome 11

Paternal uniparental disomy for chromosome 11(type), Uniparental disomy of chromosome 11
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Uniparental disomy of 11: Related Conditions

Research the causes of these diseases that are similar to, or related to, Uniparental disomy of 11:

  • Maternal UPD
  • Patenal UPD
  • Trisomic rescue
  • Rare recessive disorders
 

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