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Chromosome 18 Ring

Chromosome 18 Ring: Introduction

Chromosome 18 Ring: A rare chromosomal disorder where genetic material from one or both ends of chromosome 18 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 18 Ring is available below.

Symptoms of Chromosome 18 Ring

Wrongly Diagnosed with Chromosome 18 Ring?

Chromosome 18 Ring: Related Patient Stories

Chromosome 18 Ring: Complications

Review possible medical complications related to Chromosome 18 Ring:

Causes of Chromosome 18 Ring

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Disease Topics Related To Chromosome 18 Ring

Research the causes of these diseases that are similar to, or related to, Chromosome 18 Ring:

Statistics for Chromosome 18 Ring

Chromosome 18 Ring: Broader Related Topics

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Definitions of Chromosome 18 Ring:

Chromosome 18 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 18 Ring, or a subtype of Chromosome 18 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 18 Ring as a "rare disease".
Source - Orphanet

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More information about Chromosome 18 Ring

  1. Chromosome 18 Ring: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Complications
 

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