Glomerulonephrosis

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Glomerulonephrosis refers to a non-inflammatory disease of the kidney (nephrosis) presenting primarily in the glomerulus (a glomerulopathy.)

It can be contrasted to glomerulonephritis, which implies inflammation.

It can be caused by diethylnitrosamine.^[1]

References

Abdominal

Primarily
nephrotic

Non-proliferative	Minimal change Focal segmental Membranous

Proliferative	Mesangial proliferative Endocapillary proliferative Membranoproliferative/mesangiocapillary

By condition	Diabetic Amyloidosis

Primarily
nephritic,
RPG

Type I RPG/Type II hypersensitivity	Goodpasture's syndrome

Type II RPG/Type III hypersensitivity	Post-streptococcal Lupus DPN IgA/Berger's

Type III RPG/Pauci-immune	Granulomatosis with polyangiitis Microscopic polyangiitis Churg–Strauss syndrome

Proximal	RTA RTA 2 Fanconi syndrome

Thick ascending	Bartter syndrome

Distal convoluted	Gitelman syndrome

Collecting duct	Liddle's syndrome RTA RTA 1 Diabetes insipidus Nephrogenic

Renal papilla	Renal papillary necrosis

Major calyx/pelvis	Hydronephrosis Pyonephrosis Reflux nephropathy

Any/all	Acute tubular necrosis

Any/all

General syndromes	Renal failure Acute renal failure Chronic kidney disease Uremic pericarditis Uremia

Vascular	Renal artery stenosis Renal ischemia Hypertensive nephropathy Renovascular hypertension Renal cortical necrosis

Other	Analgesic nephropathy Renal osteodystrophy Nephroptosis Abderhalden–Kaufmann–Lignac syndrome

Pelvic

Bladder	Cystitis Interstitial cystitis Hunner's ulcer Trigonitis Hemorrhagic cystitis Neurogenic bladder dysfunction Bladder sphincter dyssynergia Vesicointestinal fistula Vesicoureteral reflux

Urethra	Urethritis Non-gonococcal urethritis Urethral syndrome Urethral stricture/Meatal stenosis Urethral caruncle

Any/all

anat/phys/devp/cell

noco/acba/cong/tumr, sysi/epon, urte

proc/itvp, drug (G4B), blte, urte

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