Related MeSH Hierarchy (4)
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Skin Diseases, Genetic » Erythrokeratodermia Variabilis
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Erythema » Erythrokeratodermia Variabilis
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Keratosis » Erythrokeratodermia Variabilis
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Genetic » Erythrokeratodermia Variabilis
Description
An autosomal dominant skin disease characterized by transient and variable noninflammatory ERYTHEMA and hyperkeratosis. It has been associated with mutations in the genes that code for CONNEXINS. Erythrokeratodermia variabilis inherited in an autosomal recessive fashion has also been reported. Affected individuals often develop PALMOPLANTAR KERATODERMA. MeSH
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