Chromosome 10, uniparental disomy (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.
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UPD10:
»Introduction: UPD10
»Symptoms of UPD10
These medical condition or symptom topics may be relevant to medical information for Chromosome 10, uniparental disomy:
Chromosome 10, uniparental disomy: Another name for UPD10 (or close medical condition association).
»Introduction: UPD10
»Symptoms of UPD10
Some of the symptoms of Chromosome 10, uniparental disomy incude:
Read more about symptoms of Chromosome 10, uniparental disomy (UPD10)
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