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Chromosome 18, trisomy 18q

Chromosome 18, trisomy 18q: Introduction

Chromosome 18, trisomy 18q: A rare chromosomal disorder involving an extra copy of genetic material from the long arm of chromosome 18. The type and severity of symptoms are determined by the amount and location of the duplicated genetic material. More detailed information about the symptoms, causes, and treatments of Chromosome 18, trisomy 18q is available below.

Symptoms of Chromosome 18, trisomy 18q

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Causes of Chromosome 18, trisomy 18q

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Disease Topics Related To Chromosome 18, trisomy 18q

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Chromosome 18, trisomy 18q: Research Doctors & Specialists

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Hospitals & Clinics: Chromosome 18, trisomy 18q

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Chromosome 18, trisomy 18q: Broader Related Topics

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Definitions of Chromosome 18, trisomy 18q:

Chromosome 18, trisomy 18q 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 18q, or a subtype of Chromosome 18, trisomy 18q, 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 18q

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

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