EB43 Epidermolysis bullosa acquisita

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01


Epidermolysis bullosa acquisita is an acquired non-familial blistering disease characterised by the presence of autoantibodies to collagen VII at the epidermal basement membrane zone, as demonstrated by direct immunofluorescence. There is a wide spectrum of clinical manifestations including a trauma-induced variant and a more inflammatory variant.

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