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Dictionary » Mosaic trisomy 21
 

Mosaic trisomy 21

Introduction: Mosaic trisomy 21

Description of Mosaic trisomy 21

Mosaic trisomy 21 (medical condition): A rare chromosomal disorder where an extra copy of chromosome 16...more »

See also:

Chromosome 21, uniparental disomy of:
  »Introduction: Chromosome 21, uniparental disomy of
  »Symptoms of Chromosome 21, uniparental disomy of

Mosaic trisomy 21: Related Topics

These medical condition or symptom topics may be relevant to medical information for Mosaic trisomy 21:

Mosaic trisomy 21: Rare Disease

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

Mosaic trisomy 21 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Mosaic trisomy 21, or a subtype of Mosaic trisomy 21, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Mosaic trisomy 21 as a Disease

Mosaic trisomy 21: Another name for Chromosome 21, uniparental disomy of (or close medical condition association).
  »Introduction: Chromosome 21, uniparental disomy of
  »Symptoms of Chromosome 21, uniparental disomy of

Mosaic trisomy 21: Related Diseases

Mosaic trisomy 21: Mosaic trisomy 21 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Mosaic trisomy 21 (Chromosome 21, uniparental disomy of)

Some of the symptoms of Mosaic trisomy 21 incude:

  • Embryonic failure

Terms associated with Mosaic trisomy 21:

Terms Similar to Mosaic trisomy 21:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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