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Disease Ontology Browser
Behcet's disease (DOID:13241)
Alliance: disease page
Synonyms: Adamantiades-Behcet disease; Behcet syndrome; Behcet's syndrome; Behet's syndrome; triple symptom complex
Alt IDs: OMIM:109650, EFO:0003780, ICD10CM:M35.2, ICD9CM:136.1, ICD9CM_2006:136.1, MESH:D001528, NCI:C34416, UMLS_CUI:C0004943
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.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
09/30/2025
MGI 6.24
The Jackson Laboratory