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Chromosome 18, trisomy 18p

Chromosome 18, trisomy 18p: Introduction

Chromosome 18, trisomy 18p: A rare chromosomal disorder where a portion of the short arm (p) is duplicated resulting in various abnormalities. More detailed information about the symptoms, causes, and treatments of Chromosome 18, trisomy 18p is available below.

Symptoms of Chromosome 18, trisomy 18p

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Causes of Chromosome 18, trisomy 18p

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Disease Topics Related To Chromosome 18, trisomy 18p

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Chromosome 18, trisomy 18p: Research Doctors & Specialists

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Hospitals & Clinics: Chromosome 18, trisomy 18p

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Chromosome 18, trisomy 18p: Broader Related Topics

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Definitions of Chromosome 18, trisomy 18p:

Chromosome 18, trisomy 18p is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 18, trisomy 18p, or a subtype of Chromosome 18, trisomy 18p, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Chromosome 18, trisomy 18p

  1. Chromosome 18, trisomy 18p: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Home Testing
 

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