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Chromosome 18, deletion 18q23

Chromosome 18, deletion 18q23: Introduction

Chromosome 18, deletion 18q23: A very rare syndrome caused by a deletion of a part of the material on chromosome 18 and resulting in various abnormalities such as retarded growth, hearing loss and mental retardation. The abnormalities vary from patient to patient. More detailed information about the symptoms, causes, and treatments of Chromosome 18, deletion 18q23 is available below.

Symptoms of Chromosome 18, deletion 18q23

Causes of Chromosome 18, deletion 18q23

Read more about causes of Chromosome 18, deletion 18q23.

Statistics for Chromosome 18, deletion 18q23

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Definitions of Chromosome 18, deletion 18q23:

Chromosome 18, deletion 18q23 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, deletion 18q23, or a subtype of Chromosome 18, deletion 18q23, 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, deletion 18q23

  1. Chromosome 18, deletion 18q23: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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