Chromosome 10, uniparental disomy of (medical condition): A rare chromosomal disorder where the offspring inherits a both copies of chromosome 10 from one parent rather than one chromosome from each parent. No clinical symptoms have been reported on this defect and is generally believed to be harmless on its own.
See also:
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
These medical condition or symptom topics may be relevant to medical information for Chromosome 10, uniparental disomy of:
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 (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
Source - NIH
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