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X chromosome, trisomy Xq25: A condition characterised by the duplication of the long arm of chromosome X. More detailed information about the symptoms, causes, and treatments of X chromosome, trisomy Xq25 is available below.
See full list of 14 symptoms of X chromosome, trisomy Xq25
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Read more about causes of X chromosome, trisomy Xq25.
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Types of X chromosome, trisomy Xq25
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X chromosome, trisomy Xq25 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that X chromosome, trisomy Xq25, or a subtype of X chromosome, trisomy Xq25,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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