Cardioectodermal syndrome
MONDO:0100080A 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
0 clinical trials for this condition and its sub-types, 0 tagged with Cardioectodermal syndrome itself.
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Sub-types of Cardioectodermal syndrome
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Naxos disease 0 trials
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