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Dictionary » Uniparental disomy of 13
 

Uniparental disomy of 13

Introduction: Uniparental disomy of 13

Description of Uniparental disomy of 13

Uniparental disomy of 13 (medical condition): A condition which is characterized by the uniparental disomy of...more »

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Uniparental disomy of 13:
  »Introduction: Uniparental disomy of 13
  »Symptoms of Uniparental disomy of 13
  »Treatments for Uniparental disomy of 13

Uniparental disomy of 13: Related Topics

These medical condition or symptom topics may be relevant to medical information for Uniparental disomy of 13:

Uniparental disomy of 13: Rare Disease

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

Uniparental disomy of 13 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Uniparental disomy of 13, or a subtype of Uniparental disomy of 13, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Uniparental disomy of 13 as a Disease

Uniparental disomy of 13 (medical condition): See Uniparental disomy of 13 (disease information).
  »Introduction: Uniparental disomy of 13
  »Symptoms of Uniparental disomy of 13
  »Treatments for Uniparental disomy of 13

Uniparental disomy of 13: Related Diseases

Uniparental disomy of 13: Uniparental disomy of 13 is listed as a type of (or associated with) the following medical conditions in our database:

More information on medical condition: Uniparental disomy of 13:

Terms associated with Uniparental disomy of 13:

Terms Similar to Uniparental disomy of 13:

Source - NIH

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