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Ankyloblepharon-ectodermal defects-cleft lip/palate (medical condition): A rare genetic disorder characterized by ankyloblepharon, ectodermal...more »
See also:
Hay-Wells Syndrome:
»Introduction: Hay-Wells Syndrome
»Symptoms of Hay-Wells Syndrome
These medical condition or symptom topics may be relevant to medical information for Ankyloblepharon-ectodermal defects-cleft lip/palate:
Ankyloblepharon-ectodermal defects-cleft lip/palate is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Ankyloblepharon-ectodermal defects-cleft lip/palate, or a subtype of Ankyloblepharon-ectodermal defects-cleft lip/palate,
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 if affects 1 person per 2,000.
They list Ankyloblepharon-ectodermal defects-cleft lip/palate as a "rare disease".
Source - Orphanet
Ankyloblepharon-ectodermal defects-cleft lip/palate: Another name for Hay-Wells Syndrome (or close medical condition association).
»Introduction: Hay-Wells Syndrome
»Symptoms of Hay-Wells Syndrome
Ankyloblepharon-ectodermal defects-cleft lip/palate: Ankyloblepharon-ectodermal defects-cleft lip/palate is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of Ankyloblepharon-ectodermal defects-cleft lip/palate incude:
See full list of 29 symptoms of Ankyloblepharon-ectodermal defects-cleft lip/palate (Hay-Wells Syndrome)
These medical disease topics may be related to Ankyloblepharon-ectodermal defects-cleft lip/palate:
Source - NIH
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