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Chromosome 1, deletion q21 q25

Chromosome 1, deletion q21 q25: Introduction

Chromosome 1, deletion q21 q25: A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as retarded fetal growth, osteoporosis, facial anomalies and hearing loss. More detailed information about the symptoms, causes, and treatments of Chromosome 1, deletion q21 q25 is available below.

Symptoms of Chromosome 1, deletion q21 q25

Causes of Chromosome 1, deletion q21 q25

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Definitions of Chromosome 1, deletion q21 q25:

Chromosome 1, deletion q21 q25 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 1, deletion q21 q25, or a subtype of Chromosome 1, deletion q21 q25, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Chromosome 1, deletion q21 q25

  1. Chromosome 1, deletion q21 q25: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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