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Glomerulopathies

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Glomerulopathies

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Nephrotic syndrome without extrarenal manifestations Nephrotic syndrome, idiopathic Idiopathic steroid-sensitive nephrotic syndrome Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance Idiopathic steroid-resistant nephrotic syndrome Idiopathic multidrug-resistant nephrotic syndrome Idiopathic steroid-resistant nephrotic syndrome with sensitivity to second-line immunouppressive therapy Nephrotic syndrome, genetic Genetic steroid-resistant nephrotic syndrome (SRNS)Congenital nephrotic syndrome, Finnish type Congenital nephrotic syndrome, no genetic cause specified Glomerulopathy as part of a syndromic disorder Denys-Drash syndrome Frasier syndrome Galloway-Mowat syndrome Schimke immuno-osseous dysplasia Pierson syndrome Nail-patella syndrome Leigh syndrome with nephrotic syndrome Nephrotic syndrome, familial, steroid-resistant (SRNS), with sensorineural deafness MYH9-related disease Familial steroid-resistant nephrotic syndrome with adrenal insufficiency Nephrotic syndrome-deafness-pretibial epidermolysis bullosa syndrome Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome Autosomal dominant intermediate Charcot-Marie-Tooth disease type E Severe oculo-renal-cerebellar syndrome Action myoclonus-renal failure syndrome Fibronectin glomerulopathy Lipoprotein glomerulopathy Collagen type III glomerulopathy Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization Nephrotic syndrome, syndromic, not otherwise specified IgA nephropathy Membranous glomerulonephritis Collagenopathies (inc. Alport syndrome)Alport syndrome Alport syndrome, X-linked Alport syndrome, X-linked with diffuse leiomyomatosis Alport syndrome, autosomal dominant Alport syndrome, autosomal recessive Alport syndrome, digenic Microscopic (including familial) hematuria Collagenopathy, not further specified HANAC syndrome Primary membranoproliferative glomerulonephritis (MPGN)Immunoglobulin-mediated membranoproliferative glomerulonephritis (MPGN)C3 glomerulopathy Dense deposit disease C3 glomerulonephritis Glomerulopathy as part of a systemic disorder Glomerulopathy as part of a genetic systemic disease Familial Mediterranean fever Muckle-Wells syndrome Hypocomplementemic urticarial vasculitis Hereditary amyloidosis with primary renal involement AApoAI amyloidosis ALys amyloidosis AFib amyloidosis AApoAII amyloidosis Autoimmune interstitial lung disease-arthritis syndrome Glomerulopathy as part of a non-genetic systemic disease Systemic vasculitis associated with glomerulopathy Systemic Lupus Erythematosus (SLE)Childhood-onset systemic lupus erythematosus (SLE)Granulomatosis with polyangiitis (Wegener)Immunoglobulin A vasculitis (Henoch Schonlein nephritis, PSH)Pauci-immune glomerulonephritis Pauci-immune glomerulonephritis with ANCA Pauci-immune glomerulonephritis without ANCA Microscopic polyangiitis Eosinophilic granulomatosis with polyangiitis Polyarteritis nodosa Takayasu arteritis Giant cell arteritis Relapsing polychondritis Buerger disease Cryoglobulinemic vasculitis Anti-glomerular basement membrane disease Mixed connective tissue disease Monoclonal gammopathy of renal significance (MGRS)C3 glomerulopathy secondary to MGRS Proliferative glomerulonephritis with monoclonal immune deposits (PGNMID)AA amyloidosis AL amyloidosis Primary systemic amyloidosis Primary localized amyloidosis AH amyloidosis AApoAIV amyloidosis Non-amyloid monoclonal immunoglobulin deposition disease Heavy chain deposition disease Light and heavy chain deposition disease Light chain deposition disease IgG4-related kidney disease Polymyositis Juvenile polymyositis Dermatomyositis Juvenile dermatomyositis Beh Sarcoidosis Adult-onset Still disease Reynolds syndrome Systemic sclerosis CREST syndrome Diffuse cutaneous systemic sclerosis Limited cutaneous systemic sclerosis Limited systemic sclerosis Immunotactoid or fibrillary glomerulopathy Non-amyloid fibrillary glomerulopathy Immunotactoid glomerulopathy Idiopathic non-lupus full-house nephropathy

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