Other necrotizing vasculopathies (FG)

Description

vasculitis: 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. BehC'et disease, see this term) to relatively minor skin disease.

Data source
FinnGen phenocode NECROVASC_FG
Include M13_WEGENER, M13_TAKAYASU, GIANT_CELL_TEMP_ARTERITIS, M13_MICROPOLYANG, M13_NECROVASCNAS
First defined in version DF2
Ontology
DOID 865
GWAS catalog 0006803
MESH D056647
SNOMED CT 31996006

Key figures

Sex All Female Male
Number of individuals 588 371 217
Unadjusted prevalence (%) 0.34 0.37 0.29
Mean age at first event (years) 60.01 60.37 59.39
Case fatality at 5-years (%) 7.65 5.93 10.6

Longitudinal metrics

Sex All Female Male
Median nb. of events per indiv. 3 3 4
Recurrence at 6 months (%) 59.18 57.14 62.67

Associations

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