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What is Chromosome 3, monosomy 3q21-23?

What is Chromosome 3, monosomy 3q21-23?

  • Chromosome 3, monosomy 3q21-23: A very rare chromosomal disorder involving the deletion of a part of the long arm of chromosome 3 which results mainly in eye abnormalities.

Chromosome 3, monosomy 3q21-23 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 3, monosomy 3q21-23, or a subtype of Chromosome 3, monosomy 3q21-23, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Chromosome 3, monosomy 3q21-23: Introduction

Types of Chromosome 3, monosomy 3q21-23:

Broader types of Chromosome 3, monosomy 3q21-23:

What causes Chromosome 3, monosomy 3q21-23?

Causes of Chromosome 3, monosomy 3q21-23: see causes of Chromosome 3, monosomy 3q21-23

What are the symptoms of Chromosome 3, monosomy 3q21-23?

Symptoms of Chromosome 3, monosomy 3q21-23: see symptoms of Chromosome 3, monosomy 3q21-23

How is it treated?

Doctors and Medical Specialists for Chromosome 3, monosomy 3q21-23: Medical Geneticist ; see also doctors and medical specialists for Chromosome 3, monosomy 3q21-23.
Treatments for Chromosome 3, monosomy 3q21-23: see treatments for Chromosome 3, monosomy 3q21-23

Name and Aliases of Chromosome 3, monosomy 3q21-23

Main name of condition: Chromosome 3, monosomy 3q21-23

Other names or spellings for Chromosome 3, monosomy 3q21-23:

Monosomy 3q21 23, Deletion 3q21 23

Deletion 3q21 23, Monosomy 3q21 23
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

 

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