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PedAM

Pediatric Disease Annotations & Medicines




Disease ectodermal dysplasia
Phenotype C0349788|arrhythmogenic right ventricular cardiomyopathy
Sentences 1
PubMedID- 26137453 Reported the r298q mutation of p63 gene in autosomal dominant ectodermal dysplasia associated with arrhythmogenic right ventricular cardiomyopathy (31).

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