Wegener's granulomatosis
E105929
Wegener's granulomatosis, now more commonly called granulomatosis with polyangiitis, is a rare autoimmune disease characterized by inflammation of blood vessels that can damage organs such as the lungs, kidneys, and upper respiratory tract.
All labels observed (7)
| Label | Occurrences |
|---|---|
| granulomatosis with polyangiitis | 3 |
| ANCA-associated vasculitis | 1 |
| Wegener | 1 |
| Wegener granulomatosis | 1 |
| Wegener vasculitis | 1 |
| Wegener's granulomatosis canonical | 1 |
| granulomatosis with polyangiitis (Wegener's) | 1 |
Statements (65)
| Predicate | Object |
|---|---|
| instanceOf |
autoimmune disease
ⓘ
granulomatous disease ⓘ rare disease ⓘ systemic vasculitis ⓘ |
| affectsSystem |
lower respiratory tract
ⓘ
renal system ⓘ respiratory system ⓘ upper respiratory tract ⓘ vascular system ⓘ |
| associatedWithAntibody | anti-proteinase 3 antibody ⓘ |
| canCause |
chronic sinusitis
ⓘ
glomerulonephritis ⓘ hematuria ⓘ otitis media ⓘ proteinuria ⓘ pulmonary hemorrhage ⓘ pulmonary nodules ⓘ saddle-nose deformity ⓘ |
| hasAbbreviation | GPA ⓘ |
| hasBiomarker |
PR3-ANCA
ⓘ
c-ANCA ⓘ |
| hasClassification |
Wegener's granulomatosis
self-linksurface differs
ⓘ
surface form:
ANCA-associated vasculitis
small-vessel vasculitis ⓘ |
| hasCourse | chronic relapsing course ⓘ |
| hasDiagnosticTest |
ANCA test
ⓘ
chest CT scan ⓘ tissue biopsy ⓘ urinalysis ⓘ |
| hasEponym | Friedrich Wegener ⓘ |
| hasEtiology | autoimmune mechanism ⓘ |
| hasICD10Code | M31.3 ⓘ |
| hasPathologyFeature |
medium-vessel vasculitis
ⓘ
necrotizing granulomatous inflammation ⓘ necrotizing vasculitis ⓘ small-vessel vasculitis ⓘ |
| hasPreferredName |
Wegener's granulomatosis
self-linksurface differs
ⓘ
surface form:
granulomatosis with polyangiitis
|
| hasPrognosis | potentially life-threatening ⓘ |
| hasSymptom |
arthralgia
ⓘ
cough ⓘ dyspnea ⓘ epistaxis ⓘ fatigue ⓘ fever ⓘ hemoptysis ⓘ nasal congestion ⓘ weight loss ⓘ |
| hasSynonym |
Wegener's granulomatosis
self-linksurface differs
ⓘ
surface form:
Wegener granulomatosis
Wegener's granulomatosis self-linksurface differs ⓘ
surface form:
Wegener vasculitis
Wegener's granulomatosis self-linksurface differs ⓘ
surface form:
granulomatosis with polyangiitis (Wegener's)
|
| hasTreatmentPhase |
induction therapy
ⓘ
maintenance therapy ⓘ |
| moreCommonIn |
adults
ⓘ
middle-aged individuals ⓘ |
| recognizedBy |
American College of Rheumatology
ⓘ
Chapel Hill Consensus Conference on Vasculitis Nomenclature ⓘ |
| treatedWith |
azathioprine
ⓘ
cyclophosphamide ⓘ glucocorticoids ⓘ methotrexate ⓘ mycophenolate mofetil ⓘ Rituxan ⓘ
surface form:
rituximab
|
| typicalLesionSite |
kidneys
ⓘ
lungs ⓘ nasal cavity ⓘ paranasal sinuses ⓘ |
Referenced by (9)
Full triples — surface form annotated when it differs from this entity's canonical label.
this entity surface form:
granulomatosis with polyangiitis
this entity surface form:
granulomatosis with polyangiitis (Wegener's)
this entity surface form:
Wegener granulomatosis
this entity surface form:
Wegener vasculitis
this entity surface form:
ANCA-associated vasculitis
this entity surface form:
granulomatosis with polyangiitis
this entity surface form:
granulomatosis with polyangiitis
this entity surface form:
Wegener