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Prevalence and Incidence of Acromesomelic dysplasia Hunter Thompson type

Acromesomelic dysplasia Hunter Thompson type: Rare Disease

Acromesomelic dysplasia Hunter Thompson type is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Acromesomelic dysplasia Hunter Thompson type, or a subtype of Acromesomelic dysplasia Hunter Thompson type, 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 Acromesomelic dysplasia Hunter Thompson type as a "rare disease". More information about Acromesomelic dysplasia Hunter Thompson type is available from Orphanet

About prevalence and incidence statistics:

The term 'prevalence' of Acromesomelic dysplasia Hunter Thompson type usually refers to the estimated population of people who are managing Acromesomelic dysplasia Hunter Thompson type at any given time. The term 'incidence' of Acromesomelic dysplasia Hunter Thompson type refers to the annual diagnosis rate, or the number of new cases of Acromesomelic dysplasia Hunter Thompson type 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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