Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Skin Diseases, Genetic » Keratoderma, Palmoplantar
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Keratosis » Keratoderma, Palmoplantar
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Genetic » Keratoderma, Palmoplantar
Description
Group of mostly hereditary disorders characterized by thickening of the palms and soles as a result of excessive keratin formation leading to hypertrophy of the stratum corneum (hyperkeratosis). MeSH
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Subtype Terms (2)
Approved Indicated Drugs (1)
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UMLS Data
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