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Chromosome 9 inversion or duplication: A very rare genetic disorder where a portion of chromosome 9 is inverted or 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 inversion or duplication is available below.
See full list of 12 symptoms of Chromosome 9 inversion or duplication
Read more about treatments for Chromosome 9 inversion or duplication
Read more about causes of Chromosome 9 inversion or duplication.
Prognosis for Chromosome 9 inversion or duplication: 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.
More about prognosis of Chromosome 9 inversion or duplication
Types of Chromosome 9 inversion or duplication
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Chromosome 9 inversion or duplication 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 inversion or duplication, or a subtype of Chromosome 9 inversion or duplication,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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