Treatments & Interventions
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Buccal aphthous ulcers
Very frequent (80-99%)HP:0011107
Inflammation of blood vessel
Very frequent (80-99%)HP:0002633
Inflammation of testicles
Very frequent (80-99%)HP:0100796
Joint inflammation
Very frequent (80-99%)HP:0001369
Meningitis
Very frequent (80-99%)HP:0001287
Migraine headache
Very frequent (80-99%)HP:0002076
Mouth ulcer
Very frequent (80-99%)HP:0000155
Multiple, subcutaneous nodules
Very frequent (80-99%)HP:0001482
Muscle pain
Very frequent (80-99%)HP:0003326
Nausea and vomiting
Very frequent (80-99%)HP:0002017
Papules
Very frequent (80-99%)HP:0200034
Photophobia
Very frequent (80-99%)HP:0000613
Pyrexia
Very frequent (80-99%)HP:0001945
Tiredness
Very frequent (80-99%)HP:0012378
Abdominal discomfort
Frequent (30-79%)HP:0002027
Abnormal blistering of the skin
Frequent (30-79%)HP:0008066
Acne
Frequent (30-79%)HP:0001061
Arthritic pain
Frequent (30-79%)HP:0002829
Blood clot in vein
Frequent (30-79%)HP:0004936
Confusion
Frequent (30-79%)HP:0001289
Elevated C-reactive protein level
Frequent (30-79%)HP:0011227
Elevated sedimentation rate
Frequent (30-79%)HP:0003565
Erythema nodosum
Frequent (30-79%)HP:0012219
Gait disturbance
Frequent (30-79%)HP:0001288
Gastrointestinal haemorrhage
Frequent (30-79%)HP:0002239
Genital ulcers
Frequent (30-79%)HP:0003249
Headache
Frequent (30-79%)HP:0002315
Hemiparesis
Frequent (30-79%)HP:0001269
Immunologic hypersensitivity
Frequent (30-79%)HP:0100326
Increased inflammatory response
Frequent (30-79%)HP:0012649
Related Conditions
Behcet's disease with organ/system involvement(child)
Behcet's disease with multisystem involvement(child)
Behcet's syndrome, neurologic type(child)
Behcet's syndrome, vascular type(child)
Behcet's syndrome, incomplete type(child)
Behcet's syndrome, intestinal type(child)
Behcet's syndrome, complete type(child)
Behçet's disease affecting oral mucosa(child)
Demyelination of central nervous system with Behcet syndrome(child)
Ocular Behcet disease(child)
Behcet disease of skin(child)
Primary systemic vasculitis(parent)
Skin or mucosa lesion(parent)
Recurrent disease(parent)
Autoinflammatory syndrome(parent)
Autoimmune vasculitis(parent)
Quick Facts
- SNOMED CT
- 310701003
- UMLS CUI
- C0004943
- Fully Specified Name
- Behcet's syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
- Known Treatments
- 1
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.