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Chromosome 21 monosomy

Chromosome 21 monosomy: Introduction

Chromosome 21 monosomy: A rare chromosomal disorder where there is only one copy of chromosome 21 instead of the normal two leading to various abnormalities. More detailed information about the symptoms, causes, and treatments of Chromosome 21 monosomy is available below.

Symptoms of Chromosome 21 monosomy

Causes of Chromosome 21 monosomy

Read more about causes of Chromosome 21 monosomy.

Disease Topics Related To Chromosome 21 monosomy

Research the causes of these diseases that are similar to, or related to, Chromosome 21 monosomy:

Less Common Symptoms of Chromosome 21 monosomy

Statistics for Chromosome 21 monosomy

Chromosome 21 monosomy: Broader Related Topics

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Definitions of Chromosome 21 monosomy:

Chromosome 21 monosomy 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, or a subtype of Chromosome 21 monosomy, 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

  1. Chromosome 21 monosomy: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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