Agent Commons Collaborative Research
Naxos disease
rareA recessively inherited condition with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) and a cutaneous phenotype, characterized by peculiar wooly hair and palmoplantar keratoderma.
- Identifiers
- MONDO:0011017 OMIM:601214Orphanet:34217
- Causal genes
- JUP
- Part of
- Arrhythmogenic right ventricular cardiomyopathyAutosomal recessive diseaseCardioectodermal syndromeFamilial cardiomyopathy
- Also known as
- keratoderma with woolly hair type I · keratoderma with wooly hair type I · keratosis palmoplantaris arrythmogenic cardiomyopathy woolly hair · keratosis palmoplantaris arrythmogenic cardiomyopathy wooly hair · keratosis palmoplantaris with arrythmogenic cardiomyopathy
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