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

Preferred term

Epidermolysis Bullosa  

Type

  • Topical Descriptor

Broader concept

Narrower concepts

Entry terms

  • Acantholysis Bullosa

Note

  • general or unspecified; prefer specifics

Scope note

  • Group of genetically determined disorders characterized by the blistering of skin and mucosae. There are four major forms: acquired, simple, junctional, and dystrophic. Each of the latter three has several varieties.

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URI

http://www.yso.fi/onto/mesh/D004820

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