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| Term | Behcet's disease | ID (Ontology) | DOID:13241 (Human Disease) |
| Definition | An autoimmune disease that is characterized by mucocutaneous manifestations, including recurrent oral and genital ulcerations, ocular manifestations, especially chronic relapsing uveitis, and systemic vasculitis involving arteries and veins of all sizes. | ||
| Also Known As | "Adamantiades-Behcet disease" ; "Behcet syndrome" ; "Behet's syndrome" (for all, see Synonyms field below) | ||
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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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cardiovascular system disease |__autoimmune disease of cardiovascular system__ vascular disease | |__vasculitis___________________________________| immune system disease | |__primary immunodeficiency disease_____________| autoimmune disease | |__autoimmune disease of cardiovascular system__| Behcet's disease |
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autoimmune disease of cardiovascular system primary immunodeficiency disease vasculitis |
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EFO:0003780 GARD:848 ICD10CM:M35.2 ICD9CM:136.1 MESH:D001528 MIM:109650 NCI:C34416 SNOMEDCT_US_2023_03_01:310701003 UMLS_CUI:C0004943 |
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