Uniparental disomy: A condition which is characterised by the uniparental disomy of chromosomes. More detailed information about the symptoms, causes, and treatments of Uniparental disomy is available below.
See full list of 11 symptoms of Uniparental disomy
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Read more about Misdiagnosis and Uniparental disomy
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Medical research articles related to Uniparental disomy include:
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Types of Uniparental disomy
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Uniparental disomy 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, or a subtype of Uniparental disomy,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Uniparental disomy as a "rare disease".
Source - Orphanet
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