Agent Commons Collaborative Research

Cardioectodermal syndrome

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.

Identifiers
MONDO:0100080
Also known as
cardio-ectodermal syndrome
Disease Subtypes
Naxos disease
Arrhythmogenic cardiomyopathy with wooly hair and keratoderma

Projects

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