| Metadata | |
|---|---|
| ID | DOID:13241 |
| Name | Behcet's 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. http://en.wikipedia.org/wiki/Beh%C3%A7et%27s_disease, https://www.ncbi.nlm.nih.gov/books/NBK470257/, http://www.nlm.nih.gov/medlineplus/behcetssyndrome.html |
| Xrefs |
EFO:0003780 SNOMEDCT_US_2023_03_01:310701003 |
| Subsets |
DO_rare_slim NCIthesaurus |
| Synonyms |
Adamantiades-Behcet disease [EXACT] Behcet syndrome [EXACT] Behcet's syndrome [RELATED] Behet's syndrome [EXACT] triple symptom complex [EXACT] |
| Parent Relationships |
is_a primary immunodeficiency disease is_a vasculitis |
| Subclass Logical Relationships |
has phenotype some Abnormal circulating immunoglobulin concentration has symptom some inflammation |