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Chromosome 21, monosomy 21q22

Chromosome 21, monosomy 21q22: Introduction

Chromosome 21, monosomy 21q22: A rare chromosomal disorder where a portion of the long arm of chromosome 21 is deleted. More detailed information about the symptoms, causes, and treatments of Chromosome 21, monosomy 21q22 is available below.

Symptoms of Chromosome 21, monosomy 21q22

Wrongly Diagnosed with Chromosome 21, monosomy 21q22?

Chromosome 21, monosomy 21q22: Complications

Review possible medical complications related to Chromosome 21, monosomy 21q22:

Causes of Chromosome 21, monosomy 21q22

Read more about causes of Chromosome 21, monosomy 21q22.

Less Common Symptoms of Chromosome 21, monosomy 21q22

Statistics for Chromosome 21, monosomy 21q22

Chromosome 21, monosomy 21q22: Broader Related Topics

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Definitions of Chromosome 21, monosomy 21q22:

Chromosome 21, monosomy 21q22 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, monosomy 21q22, or a subtype of Chromosome 21, monosomy 21q22, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Chromosome 21, monosomy 21q22

  1. Chromosome 21, monosomy 21q22: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Complications
 

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