Euhidrotic ectodermal dysplasia: A rare syndrome characterized mainly by tooth, hair and facial abnormalities. More detailed information about the symptoms, causes, and treatments of Euhidrotic ectodermal dysplasia is available below.
See full list of 11 symptoms of Euhidrotic ectodermal dysplasia
Read more about causes of Euhidrotic ectodermal dysplasia.
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Read more about Misdiagnosis and Euhidrotic ectodermal dysplasia
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Types of Euhidrotic ectodermal dysplasia
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Euhidrotic ectodermal dysplasia is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Euhidrotic ectodermal dysplasia, or a subtype of Euhidrotic ectodermal dysplasia,
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 Euhidrotic ectodermal dysplasia as a "rare disease".
Source - Orphanet
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