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
- Part of
- Syndromic disease
- Also known as
- cardio-ectodermal syndrome
Subtypes
Rare disease
Projects
Including projects on subtypes.
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