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Hypohidrotic Ectodermal Dysplasia (HED) is a genetic human disorder which affects structures of ectodermal origin. Although there are autosomal recessive and dominant forms, X‐linked (XL) is the most frequent form of the disease. This XL‐HED phenotype is associated with mutations in the gene encoding the transmembrane protein ectodysplasin‐1 (EDA1), a member of the TNFα‐related signaling pathway....