Chromosome 16, uniparental disomy is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 16, uniparental disomy, or a subtype of Chromosome 16, uniparental disomy, affects less than 200,000 people in the US population.
The term 'prevalence' of Chromosome 16, uniparental disomy usually refers to the estimated population of people who are managing Chromosome 16, uniparental disomy at any given time. The term 'incidence' of Chromosome 16, uniparental disomy refers to the annual diagnosis rate, or the number of new cases of Chromosome 16, uniparental disomy diagnosed each year. Hence, these two statistics types can differ: a short-lived disease like flu can have high annual incidence but low prevalence, but a life-long disease like diabetes has a low annual incidence but high prevalence. For more information see about prevalence and incidence statistics.
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