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Skin and Connective Tissue Diseases > Skin Diseases > Erythema > Erythrokeratodermia Variabilis
Pathological Conditions, Signs and Symptoms > Signs and Symptoms > Skin Manifestations > Erythema > Erythrokeratodermia Variabilis
Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Erythrokeratodermia Variabilis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Erythrokeratodermia Variabilis
Skin and Connective Tissue Diseases > Skin Diseases > Keratosis > Erythrokeratodermia Variabilis

Preferred term

Erythrokeratodermia Variabilis  

Type

  • Topical Descriptor

Broader concept

Related concepts

Entry terms

  • Erythro et Keratodermia Variabilis
  • Erythrokeratodermia Figurata, Congenital Familial, in Plaques
  • Erythrokeratodermia Figurata Variabilis
  • Erythrokeratodermia, Progressive Symmetric
  • Erythrokeratodermia Variabilis with Erythema Gyratum Repens
  • Mendes De Costa Syndrome
  • Progressive Symmetric Erythrokeratodermia

Scope note

  • 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.

History note

  • 2010

In other languages

URI

http://www.yso.fi/onto/mesh/D056266

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