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Trisomy 22: A disorder that is characterised by the occurrence of three copies of chromosome 22. More detailed information about the symptoms, causes, and treatments of Trisomy 22 is available below.
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Trisomy 22 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Trisomy 22, or a subtype of Trisomy 22,
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 Trisomy 22 as a "rare disease".
Source - Orphanet
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