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| Term | epidermolysis bullosa acquisita | ID (Ontology) | DOID:4313 (Human Disease) |
| Definition | An acquired epidermolysis bullosa that is characterized by formation of recurrent blisters secondary to minor trauma in the skin and mucosa, and has_material_basis_in the development of autoantibodies to type VII collagen. | ||
| Also Known As | "acquired epidermolysis bullosa" | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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musculoskeletal system disease |__connective tissue disease_________ vesiculobullous skin disease | |__epidermolysis bullosa_____________| immune system disease | |__primary immunodeficiency disease__| epidermolysis bullosa acquisita |
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| Is a |
epidermolysis bullosa primary immunodeficiency disease connective tissue disease |
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External Crossreferences & Linkouts
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ICD10CM:L12.3 MESH:D016107 NCI:C84690 SNOMEDCT_US_2023_03_01:2772003 UMLS_CUI:C0079293 |
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