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Chromosome 9, trisomy 9q: A very rare genetic disorder where a portion of the genetic material on the long arm (q) of chromosome 9 is duplicated which results in various abnormalities. The type and severity of symptoms varies depending on the size and location of the genetic material involved. More detailed information about the symptoms, causes, and treatments of Chromosome 9, trisomy 9q is available below.
See full list of 44 symptoms of Chromosome 9, trisomy 9q
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Choosing the Best Hospital: More general information, not necessarily in relation to Chromosome 9, trisomy 9q, on hospital performance and surgical care quality:
Prognosis for Chromosome 9, trisomy 9q: The prognosis varies depending on the type and severity of symptoms that develop. Prompt diagnosis and appropriate treatment can improve prognosis and quality of life.
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Chromosome 9, trisomy 9q is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Chromosome 9, trisomy 9q, or a subtype of Chromosome 9, trisomy 9q,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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