cardioectodermal syndrome (MONDO_0100080, a Monarch Disease Ontology id) is a syndromic disease with phenotypic manifestations in the heart, skin, and/or hair. Variation in the genes of interest may occur in both an autosomal dominant inheritance pattern, or in an autosomal recessive inheritance pattern which may result in an earlier and/or more severe phenotypic presentation. Also known as: cardio-ectodermal syndrome.