Disease

Epidermolytic Hyperkeratosis

About the Disease
Autosomal Dominant Epidermolytic Ichthyosis, also known as bullous congenital ichthyosiform erythroderma of brock, is related to epidermolytic hyperkeratosis and ichthyosis, cyclic, with epidermolytic hyperkeratosis. An important gene associated with Autosomal Dominant Epidermolytic Ichthyosis is KRT1 (Keratin 1), and among its related pathways/superpathways is Keratinization. Affiliated tissues include skin, small intestine and breast, and related phenotypes are weight loss and erythroderma

Common Targets
KRT1 | KRT10

疾病靶点研报
Epidermolytic Hyperkeratosis

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