vasculitis
Findings
No curated finding names vasculitis yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Vasculitis represents a clinically heterogenous group of diseases of multifactorial etiology characterized by inflammation of either large-sized vessels (large-vessel vasculitis, e.g. Giant-cell arteritis and Takayasu arteritis), medium-sized vessels (medium-vessel vasculitis e.g. polyarteritis nodosa and Kawasaki disease), or small-sized vessels (small-vessel vasculitis, e.g. granulomatosis with polyangiitis, microscopic polyangiitis, immunoglobulin A vasculitis, and cutaneous leukocytoclastic angiitis). Vasculitis occurs at any age, may be acute or chronic, and manifests with general symptoms such as fever, weight loss and fatigue, as well as more specific clinical signs depending on the type of vessels and organs affected. The degree of severity is variable, ranging from life or sight threatening disease (e.g. Behcet disease) to relatively minor skin disease.
Definition from the Mondo Disease Ontology (MONDO:0018882), read 2026-09-29. CC BY 4.0.
Where it sits
- Narrower terms (18)
- aortitis
- arteritis
- autoimmune vasculitis
- central nervous system vasculitis
- choroiditis
- cutaneous vasculitis
- deficiency of adenosine deaminase 2
- hypersensitivity vasculitis
- immune complex mediated vasculitis
- Kawasaki disease
- livedoid vasculopathy
- lymphangitis
- necrotizing vasculitis
- phlebitis
- retinal vasculitis
- secondary vasculitis
- Shwartzman phenomenon
- vasculitis, lymphocytic, nodular