loading...| Preferred Name |
Vasculitis |
| ID |
http://www.orpha.net/ORDO/Orphanet_52759 |
| alternative_term |
Systemic vasculitis |
| 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; see these terms), medium-sized vessels (medium-vessel vasculitis e.g. polyarteritis nodosa and Kawasaki disease; see these terms), or small-sized vessels (small-vessel vasculitis, e.g. granulomatosis with polyangiitis, microscopic polyangiitis, immunoglobulin A vasculitis, and cutaneous leukocytoclastic angiitis; see these terms). 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. Behçet disease, see this term) to relatively minor skin disease. |
| definition_citation |
Orphanet |
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=52759 |
| hasDbXref |
MedDRA:10036023 ICD-11:4A44 MeSH:D056647 MeSH:D014657 MedDRA:10047115 UMLS:C0042384 |
| label |
Vasculitis |
| notation |
Category ORPHA:52759 |
| prefixIRI |
ORDO:Orphanet_52759 |
| prefLabel |
Vasculitis |
| present_in |
Europe AND has_point_prevalence_average_value : 6.3 AND has_point_prevalence_range : 1-9 / 100 000 |
| subClassOf |
http://www.orpha.net/ORDO/Orphanet_68362 |