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What is Chromosome 8, monosomy 8p23.1?

What is Chromosome 8, monosomy 8p23.1?

  • 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.

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)

Chromosome 8, monosomy 8p23.1: Introduction

Types of Chromosome 8, monosomy 8p23.1:

Broader types of Chromosome 8, monosomy 8p23.1:

What causes Chromosome 8, monosomy 8p23.1?

Causes of Chromosome 8, monosomy 8p23.1: see causes of Chromosome 8, monosomy 8p23.1

What are the symptoms of Chromosome 8, monosomy 8p23.1?

Symptoms of Chromosome 8, monosomy 8p23.1: see symptoms of Chromosome 8, monosomy 8p23.1

How is it treated?

Doctors and Medical Specialists for Chromosome 8, monosomy 8p23.1: Medical Geneticist ; see also doctors and medical specialists for Chromosome 8, monosomy 8p23.1.
Treatments for Chromosome 8, monosomy 8p23.1: see treatments for Chromosome 8, monosomy 8p23.1

Name and Aliases of Chromosome 8, monosomy 8p23.1

Main name of condition: Chromosome 8, monosomy 8p23.1

Other names or spellings for Chromosome 8, monosomy 8p23.1:

Monosomy 8p23 1, Deletion 8p23 1

Deletion 8p23 1, Monosomy 8p23 1
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

 

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