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Summary Literature (0)
MIM:615508 - ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IgE; EPKHE

Xenbase Genes: dsg1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014218 - severe dermatitis-multiple allergies-metabolic wasting syndrome