Aplasia cutis congenital -- intestinal lymphangiectasia: A rare disorder characterized by a skin defect and dilated intestinal lymph vessels. More detailed information about the symptoms, causes, and treatments of Aplasia cutis congenital -- intestinal lymphangiectasia is available below.
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Aplasia cutis congenital -- intestinal lymphangiectasia is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Aplasia cutis congenital -- intestinal lymphangiectasia, or a subtype of Aplasia cutis congenital -- intestinal lymphangiectasia,
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 Aplasia cutis congenital -- intestinal lymphangiectasia as a "rare disease".
Source - Orphanet
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