Acrofacial dysostosis, Nager type: A rare genetic disorder characterized by underdeveloped thumbs, forearm and cheekbones as well as ear defects. More detailed information about the symptoms, causes, and treatments of Acrofacial dysostosis, Nager type is available below.
See full list of 19 symptoms of Acrofacial dysostosis, Nager type
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See full list of 37 occasional symptoms of Acrofacial dysostosis, Nager type
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Acrofacial dysostosis, Nager 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, Nager type, or a subtype of Acrofacial dysostosis, Nager type,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Acrofacial dysostosis, Nager type as a "rare disease".
Source - Orphanet
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