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Chromosome 3, monosomy 3q21-23

Chromosome 3, monosomy 3q21-23: Introduction

Chromosome 3, monosomy 3q21-23: A very rare chromosomal disorder involving the deletion of a part of the long arm of chromosome 3 which results mainly in eye abnormalities. More detailed information about the symptoms, causes, and treatments of Chromosome 3, monosomy 3q21-23 is available below.

Symptoms of Chromosome 3, monosomy 3q21-23

Causes of Chromosome 3, monosomy 3q21-23

Read more about causes of Chromosome 3, monosomy 3q21-23.

Statistics for Chromosome 3, monosomy 3q21-23

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Definitions of Chromosome 3, monosomy 3q21-23:

Chromosome 3, monosomy 3q21-23 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 3, monosomy 3q21-23, or a subtype of Chromosome 3, monosomy 3q21-23, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Chromosome 3, monosomy 3q21-23

  1. Chromosome 3, monosomy 3q21-23: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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