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Chromosome 18 Ring: A rare chromosomal disorder where genetic material from one or both ends of chromosome 18 is missing and the two broken ends have rejoined to form a ring. The resulting type and severity of symptoms is determined by the amount and location of genetic material missing. More detailed information about the symptoms, causes, and treatments of Chromosome 18 Ring is available below.
Review possible medical complications related to Chromosome 18 Ring:
Read more about causes of Chromosome 18 Ring.
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Chromosome 18 Ring 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 Ring, or a subtype of Chromosome 18 Ring,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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