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granulomatosis with polyangiitis (DOID:12132)
Annotations: Rat: (11) Mouse: (10) Human: (12) Chinchilla: (8) Bonobo: (11) Dog: (10) Squirrel: (8)
Parent Terms Term With Siblings Child Terms
46,XX Sex Reversal with Dysgenesis of Kidneys, Adrenals, and Lungs  
Achenbach syndrome 
Acneiform Eruptions +   
acute urate nephropathy  
AIDS-Associated Nephropathy  
allergic cutaneous vasculitis +   
alopecia areata +   
Alsing Syndrome 
ancylostomiasis +  
angioedema +   
antiphospholipid syndrome +   
anuria +   
Arnold Stickler Bourne Syndrome 
atheroembolism of kidney 
autoimmune disease of blood +   
autoimmune disease of cardiovascular system +  
autoimmune disease of endocrine system +   
autoimmune disease of exocrine system 
autoimmune disease of gastrointestinal tract +   
autoimmune disease of musculoskeletal system +   
autoimmune disease of the nervous system +   
autoimmune disease of urogenital tract +   
Bifid Nose with or without Anorectal And Renal Anomalies  
Blue Diaper Syndrome 
Boudhina Yedes Khiari syndrome 
breast disease +   
bronchiolitis obliterans +   
cercarial dermatitis 
chancroid +  
chronic ulcer of skin +   
Churg-Strauss syndrome  
CINCA syndrome  
Complement Factor H Deficiency  
contagious pustular dermatitis 
Cutaneous Fistula 
cutaneous lupus erythematosus +   
cutis laxa +   
cystic kidney disease +   
Dermal Fibrosis  
dermatitis +   
dermatomyositis +   
desquamative interstitial pneumonia  
diabetes insipidus +   
Diabetic Nephropathies +   
Dimauro Disease  
Duplication of Eyebrows with Stretchable Skin and Syndactyly 
Ectodermal Dysplasia-Skin Fragility Syndrome  
Eczematous Skin Diseases +   
Elastosis Perforans Serpiginosa 
Elliott Ludman Teebi Syndrome 
endometriosis in scar of skin 
epidermal nevus +   
epidermolytic hyperkeratosis +   
Erythema +   
erythematosquamous dermatosis 
exanthem +   
extrinsic allergic alveolitis +   
FACES Syndrome 
facial dermatosis +   
Facial Ectodermal Dysplasia  
familial juvenile hyperuricemic nephropathy +   
familial Mediterranean fever +   
filariasis +   
Flynn Aird Syndrome 
Focal Facial Dermal Dysplasia 4  
Foot Diseases +   
Genetic Skin Diseases +   
Glomerular Diseases +   
Goodpasture syndrome +   
granulomatosis with polyangiitis +   
A multisystemic disease of a complex genetic background. It is characterized by inflammation of the blood vessels (VASCULITIS) leading to damage in any number of organs. The common features include granulomatous inflammation of the RESPIRATORY TRACT and KIDNEYS. Most patients have measurable autoantibodies (ANTINEUTROPHIL CYTOPLASMIC ANTIBODIES) against MYELOBLASTIN.
hair disease +   
hand dermatosis +  
hemorrhagic fever with renal syndrome +   
hemorrhoid +   
Hernandez Fragoso Syndrome 
Herrmann Syndrome 
Hydranencephaly with Renal Aplasia-Dysplasia  
hydronephrosis +   
Hyperoxaluria +   
ichthyosis +   
Ichthyosis, Mental Retardation, Dwarfism, and Renal Impairment 
idiopathic interstitial pneumonia +   
IgG4-related disease 
immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome  
impaired renal function disease +   
Infectious Skin Diseases +   
Infundibulopelvic Dysgenesis 
Interstitial Lung Disease, Nephrotic Syndrome, and Epidermolysis Bullosa, Congenital  
Jaccoud's syndrome 
Jejunal Atresia with Renal Adysplasia 
Joubert syndrome 5  
Joubert syndrome 6  
Joubert syndrome 9  
juvenile xanthogranuloma 
keratosis +   
kidney cortex necrosis 
kidney failure +   
kidney hypertrophy 
Kidney Neoplasms +   
kidney papillary necrosis 
Kimura disease 
Lachiewicz Sibley Syndrome 
Langerhans-cell histiocytosis +   
leg dermatosis 
lipomatosis +   
Lipoprotein Glomerulopathy  
localized scleroderma +   
lupus erythematosus +   
Lymphedema-Distichiasis Syndrome with Renal Disease and Diabetes Mellitus  
lymphoid interstitial pneumonia 
Macroepiphyseal Dysplasia, McAlister Coe Type 
MASS Syndrome  
mastocytosis +   
Median Cleft Lip, Corpus Callosum, Lipoma, and Skin Polyps 
Mental Retardation, Joint Hypermobility, and Skin Laxity, with or without Metabolic Abnormalities 
Metabolic Skin Diseases +   
Microscopic Polyangiitis  
mongolian spot 
Morgellons Disease 
multicentric reticulohistiocytosis 
multiple cutaneous and mucosal venous malformations  
nail disease +   
necrobiosis lipoidica 
Necrobiotic Disorders +  
Necrolytic Migratory Erythema 
nephritis +   
nephrocalcinosis +   
Nephrogenic Fibrosing Dermopathy  
nephrolithiasis +   
nephronophthisis-like nephropathy 1  
Nephropathy with Pretibial Epidermolysis Bullosa and Deafness  
nephrosclerosis +   
noninfectious dermatoses of eyelid +  
obstructive nephropathy 
Opitz Trigonocephaly Syndrome  
orthostatic proteinuria 
Papulosquamous Skin Diseases +   
phaeohyphomycosis +  
photosensitivity disease +   
pigmentation disease +   
pneumoconiosis +   
Premature Atherosclerosis, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease 
primary hyperoxaluria +   
proteinuria +   
Pruritus +   
Pseudoatrophoderma Colli 
pulmonary fibrosis +   
pulmonary sarcoidosis  
pyelitis +   
Radiation Nephropathy  
Radiation Pneumonitis  
Radio Renal Syndrome 
reactive cutaneous fibrous lesion +  
renal agenesis +   
renal artery disease +   
renal artery obstruction +   
Renal Dysplasia - Limb Defects Syndrome 
renal fibrosis +   
renal hypertension +   
renal hypoplasia +   
renal infectious disease 
Renal Ischemia  
Renal Nutcracker Syndrome 
renal tuberculosis  
Renal Tubular Dysgenesis  
renal tubular transport disease +   
Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia due to Duplication of Mitochondrial DNA 
rheumatoid arthritis interstitial lung disease 
rosacea +   
Roy Maroteaux Kremp Syndrome 
scalp dermatosis +   
sebaceous gland disease +   
Selig Benacerraf Greene Syndrome 
Siegler Brewer Carey Syndrome 
Sjogren's syndrome +   
Skin Abnormalities +   
skin atrophy 
Skin Neoplasms +   
skin sarcoidosis 
Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, and Progressive Nephropathy 
stricture or kinking of ureter 
Surfactant Dysfunction  
Surfactant Metabolism Dysfunction, Pulmonary, 1  
Surfactant Metabolism Dysfunction, Pulmonary, 2  
Surfactant Metabolism Dysfunction, Pulmonary, 3  
Surfactant Metabolism Dysfunction, Pulmonary, 5  
sweat gland disease +   
systemic scleroderma +   
Ter Haar Syndrome  
Thrombocytopenia with Elevated Serum Iga and Renal Disease 
Thyrocerebral-Retinal Syndrome 
tyrosinemia type II  
Upton Young Syndrome 
uremia +   
urticaria +   
vascular skin disease +   
verruciform xanthoma of skin 
vesiculobullous skin disease +   
vitiligo +   
Vogt-Koyanagi-Harada disease  
Zellweger syndrome +   

Exact Synonyms: WG ;   Wegener granulomatosis ;   Wegener granulomatosis, formerly ;   Wegener's granulomatosis ;   Wegener's syndrome ;   granulomatosis with polyangiitides ;   necrotizing respiratory granulomatosis
Primary IDs: MESH:D014890
Alternate IDs: OMIM:608710 ;   RDO:0004587
Xrefs: GARD:7880
Definition Sources: MESH:D014890, https://en.wikipedia.org/wiki/Granulomatosis_with_polyangiitis

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