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Chromosome 8, monosomy 8p23.1

Chromosome 8, monosomy 8p23.1: Introduction

Chromosome 8, monosomy 8p23.1: A rare chromosomal disorder involving the deletion of a portion of the short arm of chromosome 8. The symptoms are determined by the size and exact location of the deleted portion. More detailed information about the symptoms, causes, and treatments of Chromosome 8, monosomy 8p23.1 is available below.

Symptoms of Chromosome 8, monosomy 8p23.1

Causes of Chromosome 8, monosomy 8p23.1

Read more about causes of Chromosome 8, monosomy 8p23.1.

Statistics for Chromosome 8, monosomy 8p23.1

Chromosome 8, monosomy 8p23.1: Broader Related Topics

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Definitions of Chromosome 8, monosomy 8p23.1:

Chromosome 8, monosomy 8p23.1 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 8, monosomy 8p23.1, or a subtype of Chromosome 8, monosomy 8p23.1, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Chromosome 8, monosomy 8p23.1

  1. Chromosome 8, monosomy 8p23.1: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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