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Prevalence and Incidence of Acrofacial dysostosis Rodriguez type

Acrofacial dysostosis Rodriguez type: Rare Disease

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

About prevalence and incidence statistics:

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