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X chromosome, monosomy Xp22 pter

X chromosome, monosomy Xp22 pter: Introduction

X chromosome, monosomy Xp22 pter: A condition that is characterised by the occurrence of only one X chromosome in the genotype of an individual. More detailed information about the symptoms, causes, and treatments of X chromosome, monosomy Xp22 pter is available below.

Symptoms of X chromosome, monosomy Xp22 pter

Causes of X chromosome, monosomy Xp22 pter

Read more about causes of X chromosome, monosomy Xp22 pter.

Disease Topics Related To X chromosome, monosomy Xp22 pter

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Definitions of X chromosome, monosomy Xp22 pter:

X chromosome, monosomy Xp22 pter is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that X chromosome, monosomy Xp22 pter, or a subtype of X chromosome, monosomy Xp22 pter, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about X chromosome, monosomy Xp22 pter

  1. X chromosome, monosomy Xp22 pter: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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