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Dictionary » Uniparental disomy of 11
 

Uniparental disomy of 11

Introduction: Uniparental disomy of 11

Description of Uniparental disomy of 11

Uniparental disomy of 11 (medical condition): A condition which is characterised by the uniparental disomy of chromosome...more »

See also:

Uniparental disomy of 11:
  »Introduction: Uniparental disomy of 11
  »Symptoms of Uniparental disomy of 11

Uniparental disomy of 11: Related Topics

These medical condition or symptom topics may be relevant to medical information for Uniparental disomy of 11:

Uniparental disomy of 11: Rare Disease

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

Uniparental disomy of 11 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 11, or a subtype of Uniparental disomy of 11, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Uniparental disomy of 11 as a Disease

Uniparental disomy of 11 (medical condition): See Uniparental disomy of 11 (disease information).
  »Introduction: Uniparental disomy of 11
  »Symptoms of Uniparental disomy of 11

Uniparental disomy of 11: Related Diseases

Uniparental disomy of 11: Uniparental disomy of 11 is listed as a type of (or associated with) the following medical conditions in our database:

More information on medical condition: Uniparental disomy of 11:

Uniparental disomy of 11: Related Disease Topics

These medical disease topics may be related to Uniparental disomy of 11:

  • maternal UPD
  • patenal UPD
  • trisomic rescue
  • rare recessive disorders

Terms associated with Uniparental disomy of 11:

Terms Similar to Uniparental disomy of 11:

Source - NIH

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