Related MeSH Hierarchy (4)
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Skin Abnormalities » Epidermolysis Bullosa » Epidermolysis Bullosa Acquisita
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Abnormalities » Epidermolysis Bullosa » Epidermolysis Bullosa Acquisita
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Genetic » Epidermolysis Bullosa » Epidermolysis Bullosa Acquisita
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Vesiculobullous » Epidermolysis Bullosa » Epidermolysis Bullosa Acquisita
Description
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. MeSH
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Phase 2 Indicated Drugs (1)
Organization Involved with Phase 2 Indications (2)
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UMLS Data
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