Aplasia cutis congenita -- epibulbar dermoids: A very rare syndrome characterized by increased skin pigmentation, a localized absence of skin (aplasia cutis congenital) and epibulbar dermoids (a benign eye tumor). More detailed information about the symptoms, causes, and treatments of Aplasia cutis congenita -- epibulbar dermoids is available below.
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Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Aplasia cutis congenita -- epibulbar dermoids as a "rare disease".
Source - Orphanet
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