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Chromosome 20 ring

Chromosome 20 ring: Introduction

Chromosome 20 ring: A rare chromosomal disorder where genetic material from one or both ends of chromosome 20 is missing and the two broken ends have rejoined to form a ring. The resulting type and severity of symptoms is determined by the amount and location of genetic material missing. More detailed information about the symptoms, causes, and treatments of Chromosome 20 ring is available below.

Symptoms of Chromosome 20 ring

Causes of Chromosome 20 ring

Read more about causes of Chromosome 20 ring.

Disease Topics Related To Chromosome 20 ring

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

Statistics for Chromosome 20 ring

Chromosome 20 ring: Broader Related Topics

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Definitions of Chromosome 20 ring:

Chromosome 20 ring 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 ring, or a subtype of Chromosome 20 ring, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Chromosome 20 ring as a "rare disease".
Source - Orphanet

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More information about Chromosome 20 ring

  1. Chromosome 20 ring: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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