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Chromosome 20, trisomy

Chromosome 20, trisomy: Introduction

Chromosome 20, trisomy: A rare chromosomal disorder where there are three copies of chromosome 20 rather than the normal two which results in severe abnormalities and death. More detailed information about the symptoms, causes, and treatments of Chromosome 20, trisomy is available below.

Symptoms of Chromosome 20, trisomy

Home Diagnostic Testing

Home medical testing related to Chromosome 20, trisomy:

Causes of Chromosome 20, trisomy

Read more about causes of Chromosome 20, trisomy.

Disease Topics Related To Chromosome 20, trisomy

Research the causes of these diseases that are similar to, or related to, Chromosome 20, trisomy:

  • Rrae chromosomal disorder
  • Facial deformity
  • Spinal dysplasia
  • Gastrointestinal anomalies
  • Multiple congenital malformations
  • more related diseases...»

Chromosome 20, trisomy: Research Doctors & Specialists

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Hospitals & Clinics: Chromosome 20, trisomy

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Choosing the Best Hospital: More general information, not necessarily in relation to Chromosome 20, trisomy, on hospital performance and surgical care quality:

Statistics for Chromosome 20, trisomy

Chromosome 20, trisomy: Broader Related Topics

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Definitions of Chromosome 20, trisomy:

Chromosome 20, trisomy is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 20, trisomy, or a subtype of Chromosome 20, trisomy, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Related Chromosome 20, trisomy Info

Videos about Chromosome 20, trisomy

 

More information about Chromosome 20, trisomy

  1. Chromosome 20, trisomy: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Home Testing
 

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