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Chromosome 1, monosomy 1p31 p22

Chromosome 1, monosomy 1p31 p22: Introduction

Chromosome 1, monosomy 1p31 p22: A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as mental retardation, missing teeth and small eyes and jaw. More detailed information about the symptoms, causes, and treatments of Chromosome 1, monosomy 1p31 p22 is available below.

Symptoms of Chromosome 1, monosomy 1p31 p22

Causes of Chromosome 1, monosomy 1p31 p22

Read more about causes of Chromosome 1, monosomy 1p31 p22.

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Chromosome 1, monosomy 1p31 p22: Broader Related Topics

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Definitions of Chromosome 1, monosomy 1p31 p22:

Chromosome 1, monosomy 1p31 p22 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 1, monosomy 1p31 p22, or a subtype of Chromosome 1, monosomy 1p31 p22, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Chromosome 1, monosomy 1p31 p22

  1. Chromosome 1, monosomy 1p31 p22: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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