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Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Vesiculobullous > Epidermolysis Bullosa > Epidermolysis Bullosa Simplex
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Epidermolysis Bullosa > Epidermolysis Bullosa Simplex
Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Epidermolysis Bullosa > Epidermolysis Bullosa Simplex
Skin and Connective Tissue Diseases > Skin Diseases > Skin Abnormalities > Epidermolysis Bullosa > Epidermolysis Bullosa Simplex
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Skin Abnormalities > Epidermolysis Bullosa > Epidermolysis Bullosa Simplex

Término preferido

Epidermolysis Bullosa Simplex  

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Tipo

  • mesh:Descriptor

Definición

  • A form of epidermolysis bullosa characterized by serous bullae that heal without scarring. Mutations in the genes that encode KERATIN-5 and KERATIN-14 have been associated with several subtypes of epidermolysis bullosa simplex.

Concepto genérico

Conceptos relacionados

En otras lenguas

  • Épidermolyse bulleuse simple

    francés

  • Épidermolyse bulleuse non cicatricielle à transmission autosomique dominante
  • Épidermolyse bulleuse simplex

URI

http://data.loterre.fr/ark:/67375/JVR-B3MCB7R1-L

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RDF/XML TURTLE JSON-LD Creado 12/2/90, última modificación 18/6/15