Chromosome 9, trisomy 9p: A rare chromosomal disorder where a portion of the short arm (p) of chromosome 9 is duplicated so there is three copies of it instead of the normal two. More detailed information about the symptoms, causes, and treatments of Chromosome 9, trisomy 9p is available below.
See full list of 65 symptoms of Chromosome 9, trisomy 9p
See full list of 7 treatments for Chromosome 9, trisomy 9p
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Research the causes of these diseases that are similar to, or related to, Chromosome 9, trisomy 9p:
See full list of 14 occasional symptoms of Chromosome 9, trisomy 9p
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Prognosis for Chromosome 9, trisomy 9p: The prognosis varies considerably 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 9p 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 9p, or a subtype of Chromosome 9, trisomy 9p,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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