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Chromosome 3, monosomy 3p25

Chromosome 3, monosomy 3p25: Introduction

Chromosome 3, monosomy 3p25: A rare chromosomal disorder characterized by mental retardation, short stature, deafness, extra digits, facial anomalies and various other abnormalities. More detailed information about the symptoms, causes, and treatments of Chromosome 3, monosomy 3p25 is available below.

Symptoms of Chromosome 3, monosomy 3p25

Causes of Chromosome 3, monosomy 3p25

Read more about causes of Chromosome 3, monosomy 3p25.

Disease Topics Related To Chromosome 3, monosomy 3p25

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Definitions of Chromosome 3, monosomy 3p25:

Chromosome 3, monosomy 3p25 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 3p25, or a subtype of Chromosome 3, monosomy 3p25, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Chromosome 3, monosomy 3p25

  1. Chromosome 3, monosomy 3p25: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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