Chronic renal failure, etiology uncertain (1)
Glomerulonephritis, histologically NOT examined (10)
Focal segmental glomerulosclerosis with nephrotic syndrome in children (11)
IgA nephropathy (proven by immunofluorescence, not code 76 and not code 85) (12)
Dense deposit disease membrano-proliferative GN, type II (proven by immunofluorescence and/or electron microscopy) (13)
Membranous nephropathy (14)
Membrano-proliferative GN, type I (proven by immunofluorescence and/or electron microscopy - not code 84 or 89) (15)
Rapidly progressive GN without systemic disease (crescentic, histologically confirmed, not coded elsewhere) (16)
Focal segmental glomerulosclerosis with nephrotic syndrome in adults (17)
Glomerulonephritis, histologically examined (19)
Pyelonephritis/Interstitial nephritis-cause not specified (20)
Pyelonephritis/interstitial nephritis associated with neurogenic bladder (21)
Pyelonephritis/interstitial nephritis due to congenital obstructive uropathy with or without vesico-ureteric reflux (22)
Pyelonephritis/interstitial nephritis due to acquired obstructive uropathy (23)
Pyelonephritis/interstitial nephritis due to vesico-ureteric reflux without obstruction (24)
Pyelonephritis/interstitial nephritis due to urolithiasis (25)
Pyelonephritis/interstitial nephritis due to other cause (29)
Tubulo interstitial nephritis (not pyelonephritis) (30)
Nephropathy due to analgesic drugs (31)
Nephropathy due to cisplatinum (32)
Nephropathy due to cyclosporin A (33)
Lead induced interstitial nephropathy (34)
Nephropathy caused by other specific drug (39)
Cystic kidney disease-type unspecified (40)
Polycystic kidneys, adult type (dominant) (41)
Polycystic kidneys, infantile (recessive) (42)
Medullary cystic disease, including nephronophthisis (43)
Cystic kidney disease-other specified type (49)
Hereditary/Familial nephropathy-type unspecified (50)
Hereditary nephritis with nerve deafness (Alport's syndrome) (51)
Cystinosis (52)
Primary oxalosis (53)
Fabry's disease (54)
Hereditary nephropathy-other (59)
Congenital renal hypoplasia-type unspecified (60)
Oligomeganephronic hypoplasia (61)
Congenital renal dysplasia with or without urinary tract malformation (63)
Syndrome of agenesis of abdominal muscles (Prune Belly syndrome) (66)
Renal vascular disease-type unspecified (70)
Renal vascular disease due to malignant hypertension (NO primary renal disease) (71)
Renal vascular disease due to hypertension (NO primary renal disease) (72)
Renal vascular disease due to polyarteritis (73)
Wegener's granulomatosis (74)
Ischemic renal disease / cholesterol embolism (75)
Glomerulonephritis related to liver cirrhosis (76)
Cryoglobulinemic glomerulonephrititis (78)
Renal vascular disease-classified (79)
Diabetes Type I (80)
Diabetes Type II (81)
Myelomatosis/light chain deposit disease (82)
Amyloidosis (83)
Lupus erythematosus (84)
Henoch-Schönlein purpura (85)
Goodpasture's syndrome (86)
Systemic sclerosis (scleroderma) (87)
Hemolytic Uremic syndrome including Moschcowitz syndrome (88)
Multisystem disease-other specified type (89)
Cortical or tubular necrosis (90)
Tuberculosis (91)
Gout (92)
Nephrocalcinosis and hypercalcemic nephropathy (93)
Balkan nephropathy (94)
Kidney tumor (95)
Traumatic or surgical loss of kidney (96)
Other identified renal disorders (99)