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What is Chromosome 21, uniparental disomy of?

What is Chromosome 21, uniparental disomy of?

  • Chromosome 21, uniparental disomy of: A rare chromosomal disorder where an extra copy of chromosome 16 is inherited from one parent only.

Chromosome 21, uniparental disomy of is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 21, uniparental disomy of, or a subtype of Chromosome 21, uniparental disomy of, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Chromosome 21, uniparental disomy of: Introduction

Types of Chromosome 21, uniparental disomy of:

Broader types of Chromosome 21, uniparental disomy of:

What causes Chromosome 21, uniparental disomy of?

Causes of Chromosome 21, uniparental disomy of: see causes of Chromosome 21, uniparental disomy of

What are the symptoms of Chromosome 21, uniparental disomy of?

Symptoms of Chromosome 21, uniparental disomy of: see symptoms of Chromosome 21, uniparental disomy of

Chromosome 21, uniparental disomy of: Testing

Diagnostic testing: see tests for Chromosome 21, uniparental disomy of.

Misdiagnosis: see misdiagnosis and Chromosome 21, uniparental disomy of.

How is it treated?

Doctors and Medical Specialists for Chromosome 21, uniparental disomy of: Medical Geneticist ; see also doctors and medical specialists for Chromosome 21, uniparental disomy of.
Treatments for Chromosome 21, uniparental disomy of: see treatments for Chromosome 21, uniparental disomy of

Name and Aliases of Chromosome 21, uniparental disomy of

Main name of condition: Chromosome 21, uniparental disomy of

Other names or spellings for Chromosome 21, uniparental disomy of:

Uniparental disomy of 21, Mosaic trisomy 21

Mosaic trisomy 21, Uniparental disomy of 21
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

 

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