Gastrocutaneous syndrome

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| synonyms = Peptic ulcer/hiatal hernia, multiple lentigines/cafe-au-lait spots, hypertelorism, myopia{{cite web |title=Gastrocutaneous syndrome {{!}} Genetic and Rare Diseases Information Center (GARD) – an NCATS Program |url=https://rarediseases.info.nih.gov/diseases/2438/index |website=rarediseases.info.nih.gov |access-date=17 March 2019}}

| image = Autosomal dominant - en.svg

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| caption = Gastrocutaneous syndrome is an autosomal dominant disorder.

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| field = Dermatology

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Gastrocutaneous syndrome is a rare autosomal dominant cutaneous condition characterized by multiple lentigines.{{cite book |author=Rapini, Ronald P. |author2=Bolognia, Jean L. |author3=Jorizzo, Joseph L. |title=Dermatology: 2-Volume Set |publisher=Mosby |location=St. Louis |year=2007 |isbn=978-1-4160-2999-1 }}