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Dictionary » Chromosome 10, uniparental disomy of
 

Chromosome 10, uniparental disomy of

Introduction: Chromosome 10, uniparental disomy of

Description of Chromosome 10, uniparental disomy of

Chromosome 10, uniparental disomy of (medical condition): A rare chromosomal disorder where the offspring inherits a both copies of...more »

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Chromosome 10, uniparental disomy of:
  »Introduction: Chromosome 10, uniparental disomy of
  »Symptoms of Chromosome 10, uniparental disomy of
  »Treatments for Chromosome 10, uniparental disomy of

Chromosome 10, uniparental disomy of: Related Topics

These medical condition or symptom topics may be relevant to medical information for Chromosome 10, uniparental disomy of:

Chromosome 10, uniparental disomy of: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Chromosome 10, uniparental disomy of is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 10, uniparental disomy of, or a subtype of Chromosome 10, uniparental disomy of, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Chromosome 10, uniparental disomy of as a Disease

Chromosome 10, uniparental disomy of (medical condition): See Chromosome 10, uniparental disomy of (disease information).
  »Introduction: Chromosome 10, uniparental disomy of
  »Symptoms of Chromosome 10, uniparental disomy of
  »Treatments for Chromosome 10, uniparental disomy of

Chromosome 10, uniparental disomy of: Related Diseases

Chromosome 10, uniparental disomy of: Chromosome 10, uniparental disomy of is listed as a type of (or associated with) the following medical conditions in our database:

More information on medical condition: Chromosome 10, uniparental disomy of:

Terms associated with Chromosome 10, uniparental disomy of:

Terms Similar to Chromosome 10, uniparental disomy of:

Source - NIH

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