2014 /2018 ERA-EDTA PRD Code ERA-EDTA PRD code 1996 ERA-EDTA. SNOMED CT concept identifier Convert ERA-EDTA Primary Renal Diagnosis (PRD) Term

Transcription

1 Convert Primary Renal Diagnosis (PRD) Term ERA_EDTA diagnosis C 90 Acute kidney injury Acute Renal Failure Miscellaneous renal disorders C 90 Acute kidney injury due to hypovolaemia Acute Renal Failure Miscellaneous renal disorders C 90 Acute kidney injury due to circulatory failure Acute Renal Failure Miscellaneous renal disorders C 90 Acute kidney injury due to sepsis Acute Renal Failure Miscellaneous renal disorders C 90 Acute kidney injury due to rhabdomyolysis Acute Renal Failure Miscellaneous renal disorders C 90 Acute kidney injury due to nephrotoxicity Acute Renal Failure Miscellaneous renal disorders R Acute cortical necrosis Acute Renal Failure Miscellaneous renal disorders C Acute pyelonephritis Acute Renal Failure Miscellaneous renal disorders C 99 Cardiorenal syndrome Cardiorenal syndrome Other systemic diseases affecting the kidney R Autosomal dominant (AD) polycystic kidney disease Cystic Disease Familial / hereditary nephropathies R 41 Autosomal dominant (AD) polycystic kidney disease type I Cystic Disease Familial / hereditary nephropathies R 41 Autosomal dominant (AD) polycystic kidney disease type II Cystic Disease Familial / hereditary nephropathies R Autosomal recessive (AR) polycystic kidney disease Cystic Disease Familial / hereditary nephropathies R 40 40;49 Cystic kidney disease Cystic Disease Familial / hereditary nephropathies C 10 Adult nephrotic syndrome - no histology Glomerular Disease Glomerular disease C 10 Nephrotic syndrome of childhood - steroid sensitive - no histology Glomerular Disease Glomerular disease C 10 Congenital nephrotic syndrome (CNS) - no histology Glomerular Disease Glomerular disease C 10 Congenital nephrotic syndrome (CNS) - Finnish type - no histology Glomerular Disease Glomerular disease H 19 Congenital nephrotic syndrome (CNS) - Finnish type - histologically proven Glomerular Disease Glomerular disease H 19 Congenital nephrotic syndrome (CNS) - diffuse mesangial sclerosis Glomerular Disease Glomerular disease H Congenital nephrotic syndrome (CNS) - focal segmental glomerulosclerosis (FSGS) Glomerular Disease Glomerular disease C 10 Denys-Drash syndrome Glomerular Disease Glomerular disease C 10 Congenital nephrotic syndrome (CNS) - congenital infection Glomerular Disease Glomerular disease C 10 Minimal change nephropathy - no histology Glomerular Disease Glomerular disease H 19 Minimal change nephropathy - histologically proven Glomerular Disease Glomerular disease C 10 IgA nephropathy - no histology Glomerular Disease Glomerular disease H IgA nephropathy - histologically proven Glomerular Disease Glomerular disease C 10 Familial IgA nephropathy - no histology Glomerular Disease Glomerular disease H 12 Familial IgA nephropathy - histologically proven Glomerular Disease Glomerular disease C IgA nephropathy secondary to liver cirrhosis - no histology Glomerular Disease Glomerular disease H 12 IgA nephropathy secondary to liver cirrhosis - histologically proven Glomerular Disease Glomerular disease H 19 IgM - associated nephropathy Glomerular Disease Glomerular disease H Membranous nephropathy - idiopathic Glomerular Disease Glomerular disease H 14 Membranous nephropathy - malignancy associated Glomerular Disease Glomerular disease H 14 Membranous nephropathy - drug induced Glomerular Disease Glomerular disease H 14 Membranous nephropathy - infection associated Glomerular Disease Glomerular disease H Mesangiocapillary glomerulonephritis type 1 Glomerular Disease Glomerular disease H Mesangiocapillary glomerulonephritis type 2 (dense deposit disease) Glomerular Disease Glomerular disease H 19 Mesangiocapillary glomerulonephritis type 3 Glomerular Disease Glomerular disease H Idiopathic rapidly progressive (crescentic) glomerulonephritis Glomerular Disease Glomerular disease H Primary focal segmental glomerulosclerosis (FSGS) Glomerular Disease Glomerular disease Acute post-infectious glomerulonephritis - post-streptococcal Glomerular Disease Glomerular disease Acute post-infectious glomerulonephritis - non-streptococcal Glomerular Disease Glomerular disease C 17 Focal segmental glomerulosclerosis (FSGS) secondary to obesity - no histology Glomerular Disease Glomerular disease H 17 Focal segmental glomerulosclerosis (FSGS) secondary to obesity - histologically proven Glomerular Disease Glomerular disease Focal segmental glomerulosclerosis (FSGS) - other - no histology Glomerular Disease Glomerular disease Focal segmental glomerulosclerosis (FSGS) - other - histologically proven Glomerular Disease Glomerular disease H 19 Diffuse endocapillary glomerulonephritis Glomerular Disease Glomerular disease H 19 Mesangial proliferative glomerulonephritis Glomerular Disease Glomerular disease H 19 Focal and segmental proliferative glomerulonephritis Glomerular Disease Glomerular disease H 10 Glomerulonephritis - secondary to other systemic disease Glomerular Disease Glomerular disease H Glomerulonephritis - histologically indeterminate Glomerular Disease Glomerular disease H 70 Systemic vasculitis - ANCA negative - histologically proven Glomerular Disease Glomerular disease C 74 Systemic vasculitis - ANCA positive - no histology Glomerular Disease Glomerular disease C Granulomatosis with polyangiitis - no histology Glomerular Disease Glomerular disease H 74 Granulomatosis with polyangiitis - histologically proven Glomerular Disease Glomerular disease H 74 Microscopic polyangiitis - histologically proven Glomerular Disease Glomerular disease C 74 Churg-Strauss syndrome - no histology Glomerular Disease Glomerular disease H 74 Churg-Strauss syndrome - histologically proven Glomerular Disease Glomerular disease R Polyarteritis nodosa Glomerular Disease Glomerular disease C Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - no histology Glomerular Disease Glomerular disease H 86 Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - histologically proven Glomerular Disease Glomerular disease 1 / 5

2 Convert Primary Renal Diagnosis (PRD) Term ERA_EDTA diagnosis C Systemic lupus erythematosus / nephritis - no histology Glomerular Disease Glomerular disease H 84 Systemic lupus erythematosus / nephritis - histologically proven Glomerular Disease Glomerular disease C Henoch-Schönlein purpura / nephritis - no histology Glomerular Disease Glomerular disease H 85 Henoch-Schönlein purpura / nephritis - histologically proven Glomerular Disease Glomerular disease C Renal scleroderma / systemic sclerosis - no histology Glomerular Disease Glomerular disease H 87 Renal scleroderma / systemic sclerosis - histologically proven Glomerular Disease Glomerular disease C Essential mixed cryoglobulinaemia - no histology Glomerular Disease Glomerular disease H 78 Essential mixed cryoglobulinaemia - histologically proven Glomerular Disease Glomerular disease C 78 Cryoglobulinaemia secondary to hepatitis C - no histology Glomerular Disease Glomerular disease H 78 Cryoglobulinaemia secondary to hepatitis C - histologically proven Glomerular Disease Glomerular disease C 78 Cryoglobulinaemia secondary to systemic disease - no histology Glomerular Disease Glomerular disease H 78 Cryoglobulinaemia secondary to systemic disease - histologically proven Glomerular Disease Glomerular disease C 10 Nephrotic syndrome of childhood - steroid resistant - no histology Glomerular Disease Glomerular disease C 10 Nephrotic syndrome of childhood - no trial of steroids - no histology Glomerular Disease Glomerular disease Glomerulonephritis - no histology Glomerular Disease Glomerular disease Focal segmental glomerulosclerosis (FSGS) secondary to HIV Glomerular Disease Glomerular disease Focal segmental glomerulosclerosis (FSGS) secondary to lithium Glomerular Disease Glomerular disease Focal segmental glomerulosclerosis (FSGS) secondary to sickle cell Glomerular Disease Glomerular disease C 11 Familial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - no histology Hereditary Disease Glomerular disease H 11 Familial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - histologically proven Hereditary Disease Glomerular disease C 11 Familial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - no histology Hereditary Disease Glomerular disease H 11 Familial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - histologically proven Hereditary Disease Glomerular disease C Alport syndrome - no histology Hereditary Disease Familial / hereditary nephropathies H 51 Alport syndrome - histologically proven Hereditary Disease Familial / hereditary nephropathies C 99 Benign familial haematuria Hereditary Disease Familial / hereditary nephropathies H 99 Thin basement membrane disease Hereditary Disease Familial / hereditary nephropathies R Medullary cystic kidney disease type I Hereditary Disease Familial / hereditary nephropathies R 43 Medullary cystic kidney disease type II Hereditary Disease Familial / hereditary nephropathies C 49 Uromodulin-associated nephropathy (familial juvenile hyperuricaemic nephropathy) Hereditary Disease Familial / hereditary nephropathies C 43 Nephronophthisis Hereditary Disease Familial / hereditary nephropathies C 43 Nephronophthisis - type 1 (juvenile type) Hereditary Disease Familial / hereditary nephropathies C 43 Nephronophthisis - type 2 (infantile type) Hereditary Disease Familial / hereditary nephropathies C 43 Nephronophthisis - type 3 (adolescent type) Hereditary Disease Familial / hereditary nephropathies C 43 Nephronophthisis - type 4 (juvenile type) Hereditary Disease Familial / hereditary nephropathies C 43 Nephronophthisis - type 5 Hereditary Disease Familial / hereditary nephropathies C 43 Nephronophthisis - type 6 Hereditary Disease Familial / hereditary nephropathies C 59 Primary Fanconi syndrome Hereditary Disease Familial / hereditary nephropathies C 59 Tubular disorder as part of inherited metabolic diseases Hereditary Disease Familial / hereditary nephropathies C 30 Dent disease Hereditary Disease Familial / hereditary nephropathies C 59 Lowe syndrome (oculocerebrorenal syndrome) Hereditary Disease Familial / hereditary nephropathies C 59 Inherited aminoaciduria Hereditary Disease Familial / hereditary nephropathies C 25 Cystinuria Hereditary Disease Familial / hereditary nephropathies C Cystinosis Hereditary Disease Familial / hereditary nephropathies C 59 Inherited renal glycosuria Hereditary Disease Familial / hereditary nephropathies C 59 Hypophosphataemic rickets X-linked (XL) Hereditary Disease Familial / hereditary nephropathies C 59 Hypophosphataemic rickets autosomal recessive (AR) Hereditary Disease Familial / hereditary nephropathies C 59 Primary renal tubular acidosis (RTA) Hereditary Disease Familial / hereditary nephropathies C 59 Proximal renal tubular acidosis (RTA) - type II Hereditary Disease Familial / hereditary nephropathies C 59 Distal renal tubular acidosis (RTA) - type I Hereditary Disease Familial / hereditary nephropathies C 59 Distal renal tubular acidosis with sensorineural deafness - gene mutations Hereditary Disease Familial / hereditary nephropathies C 59 Nephrogenic diabetes insipidus Hereditary Disease Familial / hereditary nephropathies C 59 Lesch Nyhan syndrome - hypoxanthine guanine phosphoribosyl transferase deficiency Hereditary Disease Familial / hereditary nephropathies C 25 Phosphoribosyl pyrophosphate synthetase (PRPPS) superactivity Hereditary Disease Familial / hereditary nephropathies C 59 Alagille syndrome Hereditary Disease Familial / hereditary nephropathies C 59 Bartter syndrome Hereditary Disease Familial / hereditary nephropathies C 59 Gitelman syndrome Hereditary Disease Familial / hereditary nephropathies C 59 Liddle syndrome Hereditary Disease Familial / hereditary nephropathies C 59 Apparent mineralocorticoid excess Hereditary Disease Familial / hereditary nephropathies C 59 Glucocorticoid suppressible hyperaldosteronism Hereditary Disease Familial / hereditary nephropathies C 59 Inherited / genetic diabetes mellitus type II Hereditary Disease Familial / hereditary nephropathies C 59 Pseudohypoaldosteronism type 1 Hereditary Disease Familial / hereditary nephropathies C 59 Pseudohypoaldosteronism type 2 (Gordon syndrome) Hereditary Disease Familial / hereditary nephropathies 2 / 5

3 Convert Primary Renal Diagnosis (PRD) Term ERA_EDTA diagnosis C 59 Familial hypocalciuric hypercalcaemia Hereditary Disease Familial / hereditary nephropathies C 59 Familial hypercalciuric hypocalcaemia Hereditary Disease Familial / hereditary nephropathies C 59 Familial hypomagnesaemia Hereditary Disease Familial / hereditary nephropathies H Primary hyperoxaluria Hereditary Disease Familial / hereditary nephropathies C Primary hyperoxaluria Hereditary Disease Familial / hereditary nephropathies H 53 Primary hyperoxaluria type I Hereditary Disease Familial / hereditary nephropathies H 53 Primary hyperoxaluria type II Hereditary Disease Familial / hereditary nephropathies C Fabry disease - no histology Hereditary Disease Familial / hereditary nephropathies H 54 Fabry disease - histologically proven Hereditary Disease Familial / hereditary nephropathies C 59 Xanthinuria Hereditary Disease Familial / hereditary nephropathies C 59 Nail-patella syndrome Hereditary Disease Familial / hereditary nephropathies C 50 Rubinstein-Taybi syndrome Hereditary Disease Familial / hereditary nephropathies C 59 Tuberous sclerosis Hereditary Disease Familial / hereditary nephropathies C 59 Von Hippel-Lindau disease Hereditary Disease Familial / hereditary nephropathies R 25 Medullary sponge kidneys Hereditary Disease Familial / hereditary nephropathies R 99 Horse-shoe kidney Hereditary Disease Familial / hereditary nephropathies C 11 Frasier syndrome Hereditary Disease Familial / hereditary nephropathies C 59 Branchio-oto-renal syndrome Hereditary Disease Familial / hereditary nephropathies C 59 Williams syndrome Hereditary Disease Familial / hereditary nephropathies C 59 Townes-Brocks syndrome Hereditary Disease Familial / hereditary nephropathies C 59 Lawrence-Moon-Biedl / Bardet-Biedl syndrome Hereditary Disease Familial / hereditary nephropathies C 59 Mitochondrial cytopathy Hereditary Disease Familial / hereditary nephropathies C 59 50;59 Familial nephropathy Hereditary Disease Familial / hereditary nephropathies C 59 Renal coloboma syndrome Hereditary Disease Familial / hereditary nephropathies Primary hyperoxaluria type III Hereditary Disease Familial / hereditary nephropathies Kidney stones due to APRT deficiency Hereditary Disease Familial / hereditary nephropathies C 99 Hepatorenal syndrome Other Other systemic diseases affecting the kidney C Renal amyloidosis Other Other systemic diseases affecting the kidney H 83 AA amyloid secondary to chronic inflammation Other Other systemic diseases affecting the kidney H 83 AL amyloid secondary to plasma cell dyscrasia Other Other systemic diseases affecting the kidney C 83 Familial amyloid secondary to protein mutations - no histology Other Other systemic diseases affecting the kidney H 83 Familial amyloid secondary to protein mutations - histologically proven Other Other systemic diseases affecting the kidney C 83 Familial AA amyloid secondary to familial Mediterranean fever / TRAPS (Hibernian fever) - no histology Other Other systemic diseases affecting the kidney H 83 Familial AA amyloid secondary to familial Mediterranean fever / TRAPS (Hibernian fever) - histologically proven Other Other systemic diseases affecting the kidney C Myeloma kidney - no histology Other Other systemic diseases affecting the kidney H 82 Myeloma cast nephropathy - histologically proven Other Other systemic diseases affecting the kidney H 82 Light chain deposition disease Other Other systemic diseases affecting the kidney H 99 Immunotactoid / fibrillary nephropathy Other Other systemic diseases affecting the kidney C 88 Haemolytic uraemic syndrome (HUS) - diarrhoea associated Other Other systemic diseases affecting the kidney C Atypical haemolytic uraemic syndrome (HUS) - diarrhoea negative Other Other systemic diseases affecting the kidney C 88 Thrombotic thrombocytopenic purpura (TTP) Other Other systemic diseases affecting the kidney C 88 Haemolytic uraemic syndrome (HUS) secondary to systemic disease Other Other systemic diseases affecting the kidney C 88 Congenital haemolytic uraemic syndrome (HUS) Other Other systemic diseases affecting the kidney C 88 Familial haemolytic uraemic syndrome (HUS) Other Other systemic diseases affecting the kidney C 88 Familial thrombotic thrombocytopenic purpura (TTP) Other Other systemic diseases affecting the kidney C 99 Nephropathy due to eclampsia Other Other systemic diseases affecting the kidney C 89 Sickle cell nephropathy - no histology Other Other systemic diseases affecting the kidney H 89 Sickle cell nephropathy - histologically proven Other Other systemic diseases affecting the kidney R Kidney tumour Other Miscellaneous renal disorders H 95 Renal cell carcinoma - histologically proven Other Miscellaneous renal disorders H 95 Transitional cell carcinoma - histologically proven Other Miscellaneous renal disorders H 95 Wilms tumour - histologically proven Other Miscellaneous renal disorders H 95 Mesoblastic nephroma - histologically proven Other Miscellaneous renal disorders C Single kidney identified in adulthood Other Miscellaneous renal disorders C 96 Chronic kidney disease (CKD) / chronic renal failure (CRF) caused by tumour nephrectomy Other Miscellaneous renal disorders C Chronic kidney disease (CKD) / chronic renal failure (CRF) due to traumatic loss of kidney Other Miscellaneous renal disorders C 0 Chronic kidney disease (CKD) / chronic renal failure (CRF) due to donor nephrectomy Other Miscellaneous renal disorders C 0 Haematuria and proteinuria - no histology Other AND Miscellaneous renal disorders C 0 Chronic renal failure due to systemic infection Other Miscellaneous renal disorders C 0 Isolated haematuria - no histology Other Miscellaneous renal disorders C 0 Isolated proteinuria - no histology Other Miscellaneous renal disorders Infiltration by lymphoma - histologically proven Other Miscellaneous renal disorders 3 / 5

4 Convert Primary Renal Diagnosis (PRD) Term ERA_EDTA diagnosis Nephropathy due to pre-eclampsia Other Other systemic diseases affecting the kidney R 20 20;24 Primary reflux nephropathy - sporadic Tubulo-Interstitial Disease Tubulointerstitial disease R 24 Familial reflux nephropathy Tubulo-Interstitial Disease Tubulointerstitial disease R 63 60;63 Congenital dysplasia / hypoplasia Tubulo-Interstitial Disease Tubulointerstitial disease R 40 Multicystic dysplastic kidneys Tubulo-Interstitial Disease Tubulointerstitial disease R 39 Renal dysplasia due to fetal ACE-inhibitor exposure Tubulo-Interstitial Disease Tubulointerstitial disease H 49 Glomerulocystic disease Tubulo-Interstitial Disease Tubulointerstitial disease R 22 Congenital pelvi-ureteric junction obstruction Tubulo-Interstitial Disease Tubulointerstitial disease R Congenital vesico-ureteric junction obstruction Tubulo-Interstitial Disease Tubulointerstitial disease R 22 Posterior urethral valves Tubulo-Interstitial Disease Tubulointerstitial disease R Syndrome of agenesis of abdominal muscles - prune belly syndrome Tubulo-Interstitial Disease Tubulointerstitial disease R Congenital neurogenic bladder Tubulo-Interstitial Disease Tubulointerstitial disease C 29 Bladder exstrophy Tubulo-Interstitial Disease Tubulointerstitial disease R 29 Megacystis-megaureter Tubulo-Interstitial Disease Tubulointerstitial disease H Oligomeganephronia Tubulo-Interstitial Disease Tubulointerstitial disease R 99 Renal papillary necrosis - cause unknown Tubulo-Interstitial Disease Tubulointerstitial disease R Acquired obstructive uropathy / nephropathy Tubulo-Interstitial Disease Tubulointerstitial disease R 23 Acquired obstructive nephropathy due to neurogenic bladder Tubulo-Interstitial Disease Tubulointerstitial disease R 23 Obstructive nephropathy due to prostatic hypertrophy Tubulo-Interstitial Disease Tubulointerstitial disease R 23 Obstructive nephropathy due to prostate cancer Tubulo-Interstitial Disease Tubulointerstitial disease R 23 Obstructive nephropathy due to bladder cancer Tubulo-Interstitial Disease Tubulointerstitial disease R 23 Obstructive nephropathy due to other malignancies Tubulo-Interstitial Disease Tubulointerstitial disease R 23 Idiopathic retroperitoneal fibrosis Tubulo-Interstitial Disease Tubulointerstitial disease R 23 Retroperitoneal fibrosis secondary to malignancies Tubulo-Interstitial Disease Tubulointerstitial disease R Calculus nephropathy / urolithiasis Tubulo-Interstitial Disease Tubulointerstitial disease R 25 Calcium oxalate urolithiasis Tubulo-Interstitial Disease Tubulointerstitial disease C 25 Enteric hyperoxaluria Tubulo-Interstitial Disease Tubulointerstitial disease R 25 Magnesium ammonium phosphate (struvite) urolithiasis Tubulo-Interstitial Disease Tubulointerstitial disease R 25 Uric acid urolithiasis Tubulo-Interstitial Disease Tubulointerstitial disease C Tubulointerstitial nephritis - no histology Tubulo-Interstitial Disease Tubulointerstitial disease H 30 Tubulointerstitial nephritis - histologically proven Tubulo-Interstitial Disease Tubulointerstitial disease C 50 Familial interstitial nephropathy - no histology Tubulo-Interstitial Disease Tubulointerstitial disease H 30 Familial interstitial nephropathy - histologically proven Tubulo-Interstitial Disease Tubulointerstitial disease C 30 Tubulointerstitial nephritis associated with autoimmune disease - no histology Tubulo-Interstitial Disease Tubulointerstitial disease H 30 Tubulointerstitial nephritis associated with autoimmune disease - histologically proven Tubulo-Interstitial Disease Tubulointerstitial disease C 30 Tubulointerstitial nephritis with uveitis (TINU) - no histology Tubulo-Interstitial Disease Tubulointerstitial disease H 30 Tubulointerstitial nephritis with uveitis (TINU) - histologically proven Tubulo-Interstitial Disease Tubulointerstitial disease C 30 Renal sarcoidosis - no histology Tubulo-Interstitial Disease Tubulointerstitial disease H 30 Renal sarcoidosis - histologically proven Tubulo-Interstitial Disease Tubulointerstitial disease C 94 94;5 Aristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - no histology Tubulo-Interstitial Disease Tubulointerstitial disease H 94;5 Aristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - histologically proven Tubulo-Interstitial Disease Tubulointerstitial disease C Drug-induced tubulointerstitial nephritis - no histology Tubulo-Interstitial Disease Tubulointerstitial disease H 39 Drug-induced tubulointerstitial nephritis - histologically proven Tubulo-Interstitial Disease Tubulointerstitial disease C Nephropathy due to analgesic drugs - no histology Tubulo-Interstitial Disease Tubulointerstitial disease H 31 Nephropathy due to analgesic drugs - histologically proven Tubulo-Interstitial Disease Tubulointerstitial disease C Nephropathy due to ciclosporin - no histology Tubulo-Interstitial Disease Tubulointerstitial disease H 33 Nephropathy due to ciclosporin - histologically proven Tubulo-Interstitial Disease Tubulointerstitial disease C 39 Nephropathy due to tacrolimus - no histology Tubulo-Interstitial Disease Tubulointerstitial disease H 39 Nephropathy due to tacrolimus - histologically proven Tubulo-Interstitial Disease Tubulointerstitial disease C 39 Nephropathy due to aminoglycosides - no histology Tubulo-Interstitial Disease Tubulointerstitial disease H 39 Nephropathy due to aminoglycosides - histologically proven Tubulo-Interstitial Disease Tubulointerstitial disease C 39 Nephropathy due to amphotericin - no histology Tubulo-Interstitial Disease Tubulointerstitial disease H 39 Nephropathy due to amphotericin - histologically proven Tubulo-Interstitial Disease Tubulointerstitial disease C Nephropathy due to cisplatin - no histology Tubulo-Interstitial Disease Tubulointerstitial disease H 32 Nephropathy due to cisplatin - histologically proven Tubulo-Interstitial Disease Tubulointerstitial disease C 39 Nephropathy due to lithium - no histology Tubulo-Interstitial Disease Tubulointerstitial disease H 39 Nephropathy due to lithium - histologically proven Tubulo-Interstitial Disease Tubulointerstitial disease C Lead induced nephropathy - no histology Tubulo-Interstitial Disease Tubulointerstitial disease H 34 Lead induced nephropathy - histologically proven Tubulo-Interstitial Disease Tubulointerstitial disease C Acute urate nephropathy - no histology Tubulo-Interstitial Disease Tubulointerstitial disease H 92 Acute urate nephropathy - histologically proven Tubulo-Interstitial Disease Tubulointerstitial disease H 92 Chronic urate nephropathy - histologically proven Tubulo-Interstitial Disease Tubulointerstitial disease 4 / 5

5 Convert Primary Renal Diagnosis (PRD) Term ERA_EDTA diagnosis C 30 Radiation nephritis Tubulo-Interstitial Disease Tubulointerstitial disease R 99 Renal / perinephric abscess Tubulo-Interstitial Disease OR Tubulointerstitial disease C Renal tuberculosis Tubulo-Interstitial Disease Tubulointerstitial disease C 99 Leptospirosis Tubulo-Interstitial Disease Tubulointerstitial disease C 99 Hantavirus nephropathy Tubulo-Interstitial Disease Tubulointerstitial disease R 29 Xanthogranulomatous pyelonephritis Tubulo-Interstitial Disease Tubulointerstitial disease C 99 Nephropathy related to HIV - no histology Tubulo-Interstitial Disease Tubulointerstitial disease H 99 Nephropathy related to HIV - histologically proven Tubulo-Interstitial Disease Tubulointerstitial disease C 99 Schistosomiasis Tubulo-Interstitial Disease Tubulointerstitial disease C 23 Other specific infection Tubulo-Interstitial Disease Tubulointerstitial disease C 49 Renal cysts and diabetes syndrome Tubulo-Interstitial Disease Tubulointerstitial disease C 92 Chronic urate nephropathy - no histology Tubulo-Interstitial Disease Tubulointerstitial disease C Hypercalcaemic nephropathy Tubulo-Interstitial Disease Tubulointerstitial disease R 23 Retroperitoneal fibrosis secondary to peri-aortitis Tubulo-Interstitial Disease Tubulointerstitial disease C 23 Retroperitoneal fibrosis secondary to drugs Tubulo-Interstitial Disease Tubulointerstitial disease Renal papillary necrosis caused by diabetics Tubulo-Interstitial Disease Tubulointerstitial disease Renal papillary necrosis caused by analgetics Tubulo-Interstitial Disease Tubulointerstitial disease Renal papillary necrosis caused by sickle cell Tubulo-Interstitial Disease Tubulointerstitial disease C Diabetic nephropathy in type I diabetes - no histology Type 1 Diabetes Mellitus Diabetes Mellitus H 80 Diabetic nephropathy in type I diabetes - histologically proven Type 1 Diabetes Mellitus Diabetes Mellitus C Diabetic nephropathy in type II diabetes - no histology Type 2 Diabetes Mellitus Diabetes Mellitus H 81 Diabetic nephropathy in type II diabetes - histologically proven Type 2 Diabetes Mellitus Diabetes Mellitus C 0 0;29;89 Chronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - no histology Unknown Miscellaneous renal disorders H 0 Chronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - histologically proven Unknown Miscellaneous renal disorders C 99 0 Renal failure Unknown Miscellaneous renal disorders C 0 Chronic renal failure Unknown Miscellaneous renal disorders C Chronic hypertensive nephropathy - no histology Vascular Disease Hypertension / Renal vascular disease H 72 Chronic hypertensive nephropathy - histologically proven Vascular Disease Hypertension / Renal vascular disease C Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - no histology Vascular Disease Hypertension / Renal vascular disease H 71 Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - histologically proven Vascular Disease Hypertension / Renal vascular disease C 70 Ageing kidney - no histology Vascular Disease Hypertension / Renal vascular disease C Ischaemic nephropathy - no histology Vascular Disease Hypertension / Renal vascular disease H Ischaemic nephropathy / microvascular disease - histologically proven Vascular Disease Hypertension / Renal vascular disease R 70 Renal artery stenosis Vascular Disease Hypertension / Renal vascular disease C 70 70;75 Atheroembolic renal disease - no histology Vascular Disease Hypertension / Renal vascular disease H 75 Atheroembolic renal disease - histologically proven Vascular Disease Hypertension / Renal vascular disease R 70 Fibromuscular dysplasia of renal artery Vascular Disease Hypertension / Renal vascular disease R 70 Renal arterial thrombosis / occlusion Vascular Disease Hypertension / Renal vascular disease R 99 Renal vein thrombosis Vascular Disease Other systemic diseases affecting the kidney 5 / 5