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Behcet's disease
Summary
- Synonym
-
- Adamantiades-Behcet disease
- Behcet syndrome
- Behet's syndrome
- triple symptom complex
- Definition
- A vasculitis that is characterized by an autoimmune mediated inflammation of the blood vessels throughout the body leading to ulcerations on the mouth and sometimes the genitals, notorious for causing hypopyon uveitis.
- Super Class
- autoimmune disease of cardiovascular system vasculitis
External Links
- Disease Ontology
- DOID:13241
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- GARD
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 10 | NAT2 | N-acetyltransferase 2 | |
| 1234 | CCR5 | C-C motif chemokine receptor 5 | |
| 1493 | CTLA4 | cytotoxic T-lymphocyte associated protein 4 | |
| 1543 | CYP1A1 | cytochrome P450 family 1 subfamily A member 1 | |
| 1636 | ACE | angiotensin I converting enzyme | |
| 1717 | DHCR7 | 7-dehydrocholesterol reductase | |
| 2214 | FCGR3A | Fc gamma receptor IIIa | |
| 3106 | HLA-B | major histocompatibility complex, class I, B | |
| 3119 | HLA-DQB1 | major histocompatibility complex, class II, DQ beta 1 | |
| 3123 | HLA-DRB1 | major histocompatibility complex, class II, DR beta 1 |
Related Glycoprotein
