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Chromosome 9, trisomy 9q32

Chromosome 9, trisomy 9q32: Introduction

Chromosome 9, trisomy 9q32: A rare chromosomal disorder where duplication of a portion of chromosome 9 causes various abnormalities such as short stature and mental retardation and facial anomalies. More detailed information about the symptoms, causes, and treatments of Chromosome 9, trisomy 9q32 is available below.

Symptoms of Chromosome 9, trisomy 9q32

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Causes of Chromosome 9, trisomy 9q32

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Disease Topics Related To Chromosome 9, trisomy 9q32

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Chromosome 9, trisomy 9q32: Broader Related Topics

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Definitions of Chromosome 9, trisomy 9q32:

Chromosome 9, trisomy 9q32 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 9, trisomy 9q32, or a subtype of Chromosome 9, trisomy 9q32, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Chromosome 9, trisomy 9q32

  1. Chromosome 9, trisomy 9q32: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Home Testing
 

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