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Concept information

Preferred term

Erythrokeratodermia Variabilis  

Type

  • mesh:Descriptor

Definition

  • 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.

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

In other languages

  • French

  • EKV (ÉrythroKératodermie Variabilis)
  • Érythro-kératodermie variable
  • Érythrokératodermie de Mendes da Costa
  • Érythrokératodermie variable
  • Syndrome de Mendes da Costa

URI

http://data.loterre.fr/ark:/67375/JVR-GJBM8JQT-D

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RDF/XML TURTLE JSON-LD Created 7/6/09, last modified 6/20/17