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Uniparental disomy of 11: A condition which is characterised by the uniparental disomy of chromosome 11. More detailed information about the symptoms, causes, and treatments of Uniparental disomy of 11 is available below.
See full list of 11 symptoms of Uniparental disomy of 11
Home medical testing related to Uniparental disomy of 11:
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Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.
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Read more about Misdiagnosis and Uniparental disomy of 11
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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)
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