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Prevalence and Incidence of Albinism ocular late onset sensorineural deafness

Albinism ocular late onset sensorineural deafness: Rare Disease

Albinism ocular late onset sensorineural deafness is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Albinism ocular late onset sensorineural deafness, or a subtype of Albinism ocular late onset sensorineural deafness, affects less than 200,000 people in the US population.

Ophanet, who are a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list Albinism ocular late onset sensorineural deafness as a "rare disease". More information about Albinism ocular late onset sensorineural deafness is available from Orphanet

About prevalence and incidence statistics:

The term 'prevalence' of Albinism ocular late onset sensorineural deafness usually refers to the estimated population of people who are managing Albinism ocular late onset sensorineural deafness at any given time. The term 'incidence' of Albinism ocular late onset sensorineural deafness refers to the annual diagnosis rate, or the number of new cases of Albinism ocular late onset sensorineural deafness 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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