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Chromosome 18, trisomy 18q: A rare chromosomal disorder involving an extra copy of genetic material from the long arm of chromosome 18. The type and severity of symptoms are determined by the amount and location of the duplicated genetic material. More detailed information about the symptoms, causes, and treatments of Chromosome 18, trisomy 18q is available below.
See full list of 54 symptoms of Chromosome 18, trisomy 18q
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Types of Chromosome 18, trisomy 18q
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Chromosome 18, trisomy 18q is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Chromosome 18, trisomy 18q, or a subtype of Chromosome 18, trisomy 18q,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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