Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Skin Diseases, Genetic » Keratoderma, Palmoplantar » Keratoderma, Palmoplantar, Diffuse » Keratoderma, Palmoplantar, Epidermolytic
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Keratosis » Keratoderma, Palmoplantar » Keratoderma, Palmoplantar, Diffuse » Keratoderma, Palmoplantar, Epidermolytic
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Genetic » Keratoderma, Palmoplantar » Keratoderma, Palmoplantar, Diffuse » Keratoderma, Palmoplantar, Epidermolytic
Description
An autosomal dominant hereditary skin disease characterized by epidermolytic hyperkeratosis that is strictly confined to the palms and soles. It has been associated with mutations in the gene that codes for KERATIN-9. MeSH
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