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Chromosome 10, trisomy 10pter p13

Chromosome 10, trisomy 10pter p13: Introduction

Chromosome 10, trisomy 10pter p13: A rare chromosomal disorder where duplication of a portion of chromosome 10 causes various abnormalities such as a wasted build, gut and heart placement abnormalities and lack of reflexes. More detailed information about the symptoms, causes, and treatments of Chromosome 10, trisomy 10pter p13 is available below.

Symptoms of Chromosome 10, trisomy 10pter p13

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Causes of Chromosome 10, trisomy 10pter p13

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Disease Topics Related To Chromosome 10, trisomy 10pter p13

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Chromosome 10, trisomy 10pter p13: Broader Related Topics

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Definitions of Chromosome 10, trisomy 10pter p13:

Chromosome 10, trisomy 10pter p13 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 10, trisomy 10pter p13, or a subtype of Chromosome 10, trisomy 10pter p13, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Chromosome 10, trisomy 10pter p13

  1. Chromosome 10, trisomy 10pter p13: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Home Testing
 

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