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

Preferred term

Epidermolysis Bullosa Acquisita  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • Acquired Epidermolysis Bullosa
  • Acquired Form of Epidermolysis Bullosa
  • Epidermolysis Bullosa, Acquired

Note

  • note that this is acquired

Scope note

  • Form of epidermolysis bullosa characterized by trauma-induced, subepidermal blistering with no family history of the disease. Direct immunofluorescence shows IMMUNOGLOBULIN G deposited at the dermo-epidermal junction.

History note

  • 91

In other languages

URI

http://www.yso.fi/onto/mesh/D016107

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