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Dictionary » Uniparental disomy of 16
 

Uniparental disomy of 16

Introduction: Uniparental disomy of 16

Description of Uniparental disomy of 16

Uniparental disomy of 16 (medical condition): A rare chromosomal disorder where an extra copy of chromosome 16 is inherited...more »

See also:

Chromosome 16, uniparental disomy:
  »Introduction: Chromosome 16, uniparental disomy
  »Symptoms of Chromosome 16, uniparental disomy

Uniparental disomy of 16: Related Topics

These medical condition or symptom topics may be relevant to medical information for Uniparental disomy of 16:

Uniparental disomy of 16: Rare Disease

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

Uniparental disomy of 16 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 16, or a subtype of Uniparental disomy of 16, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Uniparental disomy of 16 as a Disease

Uniparental disomy of 16: Another name for Chromosome 16, uniparental disomy (or close medical condition association).
  »Introduction: Chromosome 16, uniparental disomy
  »Symptoms of Chromosome 16, uniparental disomy

Uniparental disomy of 16: Related Diseases

Uniparental disomy of 16: Uniparental disomy of 16 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Uniparental disomy of 16 (Chromosome 16, uniparental disomy)

Some of the symptoms of Uniparental disomy of 16 incude:

Terms associated with Uniparental disomy of 16:

Terms Similar to Uniparental disomy of 16:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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