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X chromosome, trisomy Xq25

X chromosome, trisomy Xq25: Introduction

X chromosome, trisomy Xq25: A condition characterised by the duplication of the long arm of chromosome X. More detailed information about the symptoms, causes, and treatments of X chromosome, trisomy Xq25 is available below.

Symptoms of X chromosome, trisomy Xq25

Home Diagnostic Testing

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Causes of X chromosome, trisomy Xq25

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Disease Topics Related To X chromosome, trisomy Xq25

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X chromosome, trisomy Xq25: Research Doctors & Specialists

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Hospitals & Clinics: X chromosome, trisomy Xq25

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Statistics for X chromosome, trisomy Xq25

X chromosome, trisomy Xq25: Broader Related Topics

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Definitions of X chromosome, trisomy Xq25:

X chromosome, trisomy Xq25 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, trisomy Xq25, or a subtype of X chromosome, trisomy Xq25, 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, trisomy Xq25

  1. X chromosome, trisomy Xq25: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Home Testing
 

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