PRDcodes
type: ValueSet
node role: treeRoot
id:
  v: PRDcodes
text:
  status:
    v: extensions
  div:
    v: Generated Narrative: ValueSet PRDcodes Include these codes as defined in https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes version ?2.17.1 Code Display Definition prd2513 2513 - AA amyloid secondary to chronic inflammation AA amyloid secondary to chronic inflammation prd1768 1768 - Acquired obstructive nephropathy due to neurogenic bladder Acquired obstructive nephropathy due to neurogenic bladder prd1752 1752 - Acquired obstructive uropathy / nephropathy Acquired obstructive uropathy / nephropathy prd3442 3442 - Acute cortical necrosis Acute cortical necrosis prd3380 3380 - Acute kidney injury Acute kidney injury prd3403 3403 - Acute kidney injury due to circulatory failure Acute kidney injury due to circulatory failure prd3398 3398 - Acute kidney injury due to hypovolaemia Acute kidney injury due to hypovolaemia prd3435 3435 - Acute kidney injury due to nephrotoxicity Acute kidney injury due to nephrotoxicity prd3426 3426 - Acute kidney injury due to rhabdomyolysis Acute kidney injury due to rhabdomyolysis prd3419 3419 - Acute kidney injury due to sepsis Acute kidney injury due to sepsis prd3457 3457 - Acute pyelonephritis Acute pyelonephritis prd2196 2196 - Acute urate nephropathy - histologically proven Acute urate nephropathy - histologically proven prd2183 2183 - Acute urate nephropathy - no histology Acute urate nephropathy - no histology prd1003 1003 - Adult nephrotic syndrome - no histology Adult nephrotic syndrome - no histology prd2392 2392 - Ageing kidney - no histology Ageing kidney - no histology prd2521 2521 - AL amyloid secondary to plasma cell dyscrasia AL amyloid secondary to plasma cell dyscrasia prd3071 3071 - Alagille syndrome Alagille syndrome prd2760 2760 - Alport syndrome - histologically proven Alport syndrome - histologically proven prd2756 2756 - Alport syndrome - no histology Alport syndrome - no histology prd1472 1472 - Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - histologically proven Anti-Glomerular basement m…
url:
  v: https://kip.rkkp.dk/fhir/ValueSet/PRDcodes
  l: PRDcodes
version:
  v: 2.17.1
name:
  v: PRDcodes
title:
  v: ERA PRD Codes
status:
  v: active
experimental:
  v: true
date:
  v: 2024-01-10T00:00:00+02:00
publisher:
  v: Sundhedsvæsenets Kvalitetsinstitut with Trifork Digital Health A/S
contact:
  name:
    v: Sundhedsvæsenets Kvalitetsinstitut with Trifork Digital Health A/S
  telecom:
    system:
      v: url
    value:
      v: https://trifork.com
  telecom:
    system:
      v: email
description:
  v: European Renal Association (ERA) Primary Renal Disease (PRD)
compose:
  include:
    system:
      v: https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes
      l: PRDcodes
    concept:
      code:
        v: prd2513
      display:
        v: 2513 - AA amyloid secondary to chronic inflammation
    concept:
      code:
        v: prd1768
      display:
        v: 1768 - Acquired obstructive nephropathy due to neurogenic bladder
    concept:
      code:
        v: prd1752
      display:
        v: 1752 - Acquired obstructive uropathy / nephropathy
    concept:
      code:
        v: prd3442
      display:
        v: 3442 - Acute cortical necrosis
    concept:
      code:
        v: prd3380
      display:
        v: 3380 - Acute kidney injury
    concept:
      code:
        v: prd3403
      display:
        v: 3403 - Acute kidney injury due to circulatory failure
    concept:
      code:
        v: prd3398
      display:
        v: 3398 - Acute kidney injury due to hypovolaemia
    concept:
      code:
        v: prd3435
      display:
        v: 3435 - Acute kidney injury due to nephrotoxicity
    concept:
      code:
        v: prd3426
      display:
        v: 3426 - Acute kidney injury due to rhabdomyolysis
    concept:
      code:
        v: prd3419
      display:
        v: 3419 - Acute kidney injury due to sepsis
    concept:
      code:
        v: prd3457
      display:
        v: 3457 - Acute pyelonephritis
    concept:
      code:
        v: prd2196
      display:
        v: 2196 - Acute urate nephropathy - histologically proven
    concept:
      code:
        v: prd2183
      display:
        v: 2183 - Acute urate nephropathy - no histology
    concept:
      code:
        v: prd1003
      display:
        v: 1003 - Adult nephrotic syndrome - no histology
    concept:
      code:
        v: prd2392
      display:
        v: 2392 - Ageing kidney - no histology
    concept:
      code:
        v: prd2521
      display:
        v: 2521 - AL amyloid secondary to plasma cell dyscrasia
    concept:
      code:
        v: prd3071
      display:
        v: 3071 - Alagille syndrome
    concept:
      code:
        v: prd2760
      display:
        v: 2760 - Alport syndrome - histologically proven
    concept:
      code:
        v: prd2756
      display:
        v: 2756 - Alport syndrome - no histology
    concept:
      code:
        v: prd1472
      display:
        v: 1472 - Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - histologically proven
    concept:
      code:
        v: prd1464
      display:
        v: 1464 - Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - no histology
    concept:
      code:
        v: prd3118
      display:
        v: 3118 - Apparent mineralocorticoid excess
    concept:
      code:
        v: prd1995
      display:
        v: 1995 - Aristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - histologically proven
    concept:
      code:
        v: prd1982
      display:
        v: 1982 - Aristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - no histology
    concept:
      code:
        v: prd2448
      display:
        v: 2448 - Atheroembolic renal disease - histologically proven
    concept:
      code:
        v: prd2430
      display:
        v: 2430 - Atheroembolic renal disease - no histology
    concept:
      code:
        v: prd2623
      display:
        v: 2623 - Atypical haemolytic uraemic syndrome (HUS) - diarrhoea negative
    concept:
      code:
        v: prd2718
      display:
        v: 2718 - Autosomal dominant (AD) polycystic kidney disease
    concept:
      code:
        v: prd2725
      display:
        v: 2725 - Autosomal dominant (AD) polycystic kidney disease type I
    concept:
      code:
        v: prd2739
      display:
        v: 2739 - Autosomal dominant (AD) polycystic kidney disease type II
    concept:
      code:
        v: prd2741
      display:
        v: 2741 - Autosomal recessive (AR) polycystic kidney disease
    concept:
      code:
        v: prd3085
      display:
        v: 3085 - Bartter syndrome

code:
  v: prd2773
display:
  v: 2773 - Benign familial haematuria

code:
  v: prd1710
display:
  v: 1710 - Bladder exstrophy

code:
  v: prd3322
display:
  v: 3322 - Branchio-oto-renal syndrome

code:
  v: prd1845
display:
  v: 1845 - Calcium oxalate urolithiasis

code:
  v: prd1832
display:
  v: 1832 - Calculus nephropathy / urolithiasis

code:
  v: prd2482
display:
  v: 2482 - Cardiorenal syndrome

code:
  v: prd2363
display:
  v: 2363 - Chronic hypertensive nephropathy - histologically proven

code:
  v: prd2359
display:
  v: 2359 - Chronic hypertensive nephropathy - no histology

code:
  v: prd3564
display:
  v: 3564 - Chronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - histologically proven

code:
  v: prd3555
display:
  v: 3555 - Chronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - no histology

code:
  v: prd3529
display:
  v: 3529 - Chronic kidney disease (CKD) / chronic renal failure (CRF) caused by tumour nephrectomy

code:
  v: prd3540
display:
  v: 3540 - Chronic kidney disease (CKD) / chronic renal failure (CRF) due to donor nephrectomy

code:
  v: prd3538
display:
  v: 3538 - Chronic kidney disease (CKD) / chronic renal failure (CRF) due to traumatic loss of kidney

code:
  v: prd3708
display:
  v: 3708 - Chronic renal failure

code:
  v: prd3643
display:
  v: 3643 - Chronic renal failure due to systemic infection

code:
  v: prd2203
display:
  v: 2203 - Chronic urate nephropathy - histologically proven

code:
  v: prd3636
display:
  v: 3636 - Chronic urate nephropathy - no histology

code:
  v: prd1440
display:
  v: 1440 - Churg-Strauss syndrome - histologically proven

code:
  v: prd1438
display:
  v: 1438 - Churg-Strauss syndrome - no histology

code:
  v: prd1625
display:
  v: 1625 - Congenital dysplasia / hypoplasia

code:
  v: prd2652
display:
  v: 2652 - Congenital haemolytic uraemic syndrome

code:
  v: prd1088
display:
  v: 1088 - Congenital nephrotic syndrome (CNS) - congenital infection

code:
  v: prd1057
display:
  v: 1057 - Congenital nephrotic syndrome (CNS) - diffuse mesangial sclerosis

code:
  v: prd1042
display:
  v: 1042 - Congenital nephrotic syndrome (CNS) - Finnish type - histologically proven

code:
  v: prd1035
display:
  v: 1035 - Congenital nephrotic syndrome (CNS) - Finnish type - no histology

code:
  v: prd1061
display:
  v: 1061 - Congenital nephrotic syndrome (CNS) - focal segmental glomerulosclerosis

code:
  v: prd1026
display:
  v: 1026 - Congenital nephrotic syndrome - no histology

code:
  v: prd1706
display:
  v: 1706 - Congenital neurogenic bladder

code:
  v: prd1660
display:
  v: 1660 - Congenital pelvi-ureteric junction obstruction

code:
  v: prd1673
display:
  v: 1673 - Congenital vesico-ureteric junction obstruction

code:
  v: prd1570
display:
  v: 1570 - Cryoglobulinaemia secondary to hepatitis C - histologically proven

code:
  v: prd1562
display:
  v: 1562 - Cryoglobulinaemia secondary to hepatitis C - no histology

code:
  v: prd1591
display:
  v: 1591 - Cryoglobulinaemia secondary to systemic disease - histologically proven

code:
  v: prd1589
display:
  v: 1589 - Cryoglobulinaemia secondary to systemic disease - no histology

code:
  v: prd2794
display:
  v: 2794 - Cystic kidney disease

code:
  v: prd2964
display:
  v: 2964 - Cystinosis

code:
  v: prd2955
display:
  v: 2955 - Cystinuria

code:
  v: prd2929
display:
  v: 2929 - Dent disease

code:
  v: prd1074
display:
  v: 1074 - Denys-Drash syndrome

code:
  v: prd2328
display:
  v: 2328 - Diabetic nephropathy in type I diabetes - histologically proven

code:
  v: prd2316
display:
  v: 2316 - Diabetic nephropathy in type I diabetes - no histology

code:
  v: prd2344
display:
  v: 2344 - Diabetic nephropathy in type II diabetes - histologically proven

code:
  v: prd2337
display:
  v: 2337 - Diabetic nephropathy in type II diabetes - no histology

code:
  v: prd1331
display:
  v: 1331 - Diffuse endocapillary glomerulonephritis

code:
  v: prd3028
display:
  v: 3028 - Distal renal tubular acidosis - type I

code:
  v: prd3037
display:
  v: 3037 - Distal renal tubular acidosis with sensorineural deafness - gene mutations

code:
  v: prd2005
display:
  v: 2005 - Drug-induced tubulointerstitial nephritis - no histology

code:
  v: prd2014
display:
  v: 2014 - Drug-induced tubulointerstitial nephritis - histologically proven

code:
  v: prd1850
display:
  v: 1850 - Enteric hyperoxaluria

code:
  v: prd1558
display:
  v: 1558 - Essential mixed cryoglobulinaemia - histologically proven

code:
  v: prd1543
display:
  v: 1543 - Essential mixed cryoglobulinaemia - no histology

code:
  v: prd3230
display:
  v: 3230 - Fabry disease - histologically proven

code:
  v: prd3224
display:
  v: 3224 - Fabry disease - no histology

code:
  v: prd2545
display:
  v: 2545 - Familial amyloid secondary to protein mutations - histologically proven

code:
  v: prd2532
display:
  v: 2532 - Familial amyloid secondary to protein mutations - no histology

code:
  v: prd1308
display:
  v: 1308 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - histologically proven

code:
  v: prd1298
display:
  v: 1298 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - no histology

code:
  v: prd1280
display:
  v: 1280 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - histologically proven

code:
  v: prd1279
display:
  v: 1279 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - no histology

code:
  v: prd2668
display:
  v: 2668 - Familial haemolytic uraemic syndrome (HUS)

code:
  v: prd3173
display:
  v: 3173 - Familial hypercalciuric hypocalcaemia

code:
  v: prd3160
display:
  v: 3160 - Familial hypocalciuric hypercalcaemia

code:
  v: prd3187
display:
  v: 3187 - Familial hypomagnesaemia

code:
  v: prd1144
display:
  v: 1144 - Familial IgA nephropathy - histologically proven

code:
  v: prd1137
display:
  v: 1137 - Familial IgA nephropathy - no histology

code:
  v: prd1911
display:
  v: 1911 - Familial interstitial nephropathy - histologically proven

code:
  v: prd1907
display:
  v: 1907 - Familial interstitial nephropathy - no histology

code:
  v: prd3379
display:
  v: 3379 - Familial nephropathy

code:
  v: prd1618
display:
  v: 1618 - Familial reflux nephropathy

code:
  v: prd2675
display:
  v: 2675 - Familial thrombotic thrombocytopenic purpura(2675)

code:
  v: prd2566
display:
  v: 2566 - Familial AA amyloid secondary to familial Mediterranean fever / TRAPS (Hibernian fever) - histologically proven

code:
  v: prd2550
display:
  v: 2550 - Familial AA amyloid secondary to familial Mediterranean fever / TRAPS (Hibernian fever) - no histology

code:
  v: prd2453
display:
  v: 2453 - Fibromuscular dysplasia of renal artery

code:
  v: prd1354
display:
  v: 1354 - Focal and segmental proliferative glomerulonephritis

code:
  v: prd3754
display:
  v: 3754 - Focal segmental glomerulosclerosis (FSGS) secondary to HIV

code:
  v: prd3765
display:
  v: 3765 - Focal segmental glomerulosclerosis (FSGS) secondary to lithium

code:
  v: prd1320
display:
  v: 1320 - Focal segmental glomerulosclerosis (FSGS) secondary to obesity - histologically proven

code:
  v: prd1312
display:
  v: 1312 - Focal segmental glomerulosclerosis (FSGS) secondary to obesity - no histology

code:
  v: prd3777
display:
  v: 3777 - Focal segmental glomerulosclerosis secondary to sickle cell

code:
  v: prd3314
display:
  v: 3314 - Frasier syndrome

code:
  v: prd3092
display:
  v: 3092 - Gitelman syndrome

code:
  v: prd1656
display:
  v: 1656 - Glomerulocystic disease

code:
  v: prd1377
display:
  v: 1377 - Glomerulonephritis - histologically indeterminate

code:
  v: prd3749
display:
  v: 3749 - Glomerulonephritis - no histology

code:
  v: prd1365
display:
  v: 1365 - Glomerulonephritis - secondary to systemic disease

code:
  v: prd3125
display:
  v: 3125 - Glucocorticoid suppressible hyperaldosteronism

code:
  v: prd1417
display:
  v: 1417 - Granulomatosis with polyangiitis - histologically proven

code:
  v: prd1401
display:
  v: 1401 - Granulomatosis with polyangiitis - no histology

code:
  v: prd3572
display:
  v: 3572 - Haematuria and proteinuria - no histology

code:
  v: prd2610
display:
  v: 2610 - Haemolytic uraemic syndrome (HUS) - diarrhoea associated

code:
  v: prd2647
display:
  v: 2647 - Haemolytic uraemic syndrome (HUS) secondary to systemic disease

code:
  v: prd2257
display:
  v: 2257 - Hantavirus nephropathy

code:
  v: prd1515
display:
  v: 1515 - Henoch-Schönlein purpura / nephritis - histologically proven

code:
  v: prd1504
display:
  v: 1504 - Henoch-Schönlein purpura / nephritis - no histology

code:
  v: prd2495
display:
  v: 2495 - Hepatorenal syndrome

code:
  v: prd3305
display:
  v: 3305 - Horse-shoe kidney

code:
  v: prd3662
display:
  v: 3662 - Hypercalcaemic nephropathy

code:
  v: prd2993
display:
  v: 2993 - Hypophosphataemic rickets autosomal recessive (AR)

code:
  v: prd2986
display:
  v: 2986 - Hypophosphataemic rickets X-linked (XL)

code:
  v: prd1251
display:
  v: 1251 - Idiopathic rapidly progressive (crescentic) glomerulonephritis

code:
  v: prd1813
display:
  v: 1813 - Idiopathic retroperitoneal fibrosis

code:
  v: prd1128
display:
  v: 1128 - IgA nephropathy - histologically proven

code:
  v: prd1116
display:
  v: 1116 - IgA nephropathy - no histology

code:
  v: prd1163
display:
  v: 1163 - IgA nephropathy secondary to liver cirrhosis - histologically proven

code:
  v: prd1159
display:
  v: 1159 - IgA nephropathy secondary to liver cirrhosis - no histology

code:
  v: prd1171
display:
  v: 1171 - IgM - associated nephropathy

code:
  v: prd2606
display:
  v: 2606 - Immunotactoid / fibrillary nephropathy

code:
  v: prd3823
display:
  v: 3823 - Infiltration by lymphoma - histologically proven

code:
  v: prd3139
display:
  v: 3139 - Inherited / genetic diabetes mellitus type II

code:
  v: prd2940
display:
  v: 2940 - Inherited aminoaciduria

code:
  v: prd2972
display:
  v: 2972 - Inherited renal glycosuria

code:
  v: prd2407
display:
  v: 2407 - Ischaemic nephropathy - no histology

code:
  v: prd2411
display:
  v: 2411 - Ischaemic nephropathy / microvascular disease - histologically proven

code:
  v: prd3712
display:
  v: 3712 - Isolated haematuria - no histology

code:
  v: prd3720
display:
  v: 3720 - Isolated proteinuria - no histology

code:
  v: prd3810
display:
  v: 3810 - Kidney stones due to ARPT deficiency

code:
  v: prd3461
display:
  v: 3461 - Kidney tumour

code:
  v: prd3351
display:
  v: 3351 - Lawrence-Moon-Biedl / Bardet-Biedl syndrome

code:
  v: prd2177
display:
  v: 2177 - Lead induced nephropathy - histologically proven

code:
  v: prd2165
display:
  v: 2165 - Lead induced nephropathy - no histology

code:
  v: prd2242
display:
  v: 2242 - Leptospirosis

code:
  v: prd3059
display:
  v: 3059 - Lesch Nyhan syndrome - hypoxanthine guanine phosphoribosyl transferase deficiency

code:
  v: prd3102
display:
  v: 3102 - Liddle syndrome

code:
  v: prd2597
display:
  v: 2597 - Light chain deposition disease

code:
  v: prd2938
display:
  v: 2938 - Lowe syndrome (oculocerebrorenal syndrome)

code:
  v: prd1866
display:
  v: 1866 - Magnesium ammonium phosphate (struvite) urolithiasis

code:
  v: prd2385
display:
  v: 2385 - Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - histologically proven

code:
  v: prd2371
display:
  v: 2371 - Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - no histology

code:
  v: prd2804
display:
  v: 2804 - Medullary cystic kidney disease type I

code:
  v: prd2815
display:
  v: 2815 - Medullary cystic kidney disease type II

code:
  v: prd3295
display:
  v: 3295 - Medullary sponge kidneys

code:
  v: prd1723
display:
  v: 1723 - Megacystis-megaureter

code:
  v: prd1205
display:
  v: 1205 - Membranous nephropathy - drug induced

code:
  v: prd1185
display:
  v: 1185 - Membranous nephropathy - idiopathic

code:
  v: prd1214
display:
  v: 1214 - Membranous nephropathy - infection associated

code:
  v: prd1192
display:
  v: 1192 - Membranous nephropathy - malignancy associated

code:
  v: prd1349
display:
  v: 1349 - Mesangial proliferative glomerulonephritis

code:
  v: prd1222
display:
  v: 1222 - Mesangiocapillary glomerulonephritis type 1

code:
  v: prd1233
display:
  v: 1233 - Mesangiocapillary glomerulonephritis type 2 (dense deposit disease)

code:
  v: prd1246
display:
  v: 1246 - Mesangiocapillary glomerulonephritis type 3

code:
  v: prd3501
display:
  v: 3501 - Mesoblastic nephroma - histologically proven

code:
  v: prd1429
display:
  v: 1429 - Microscopic polyangiitis - histologically proven

code:
  v: prd1100
display:
  v: 1100 - Minimal change nephropathy - histologically proven

code:
  v: prd1090
display:
  v: 1090 - Minimal change nephropathy - no histology

code:
  v: prd3367
display:
  v: 3367 - Mitochondrial cytopathy

code:
  v: prd1639
display:
  v: 1639 - Multicystic dysplastic kidneys

code:
  v: prd2584
display:
  v: 2584 - Myeloma cast nephropathy - histologically proven

code:
  v: prd2578
display:
  v: 2578 - Myeloma kidney - no histology

code:
  v: prd3253
display:
  v: 3253 - Nail-patella syndrome

code:
  v: prd3044
display:
  v: 3044 - Nephrogenic diabetes insipidus

code:
  v: prd2836
display:
  v: 2836 - Nephronophthisis

code:
  v: prd2843
display:
  v: 2843 - Nephronophthisis - type 1 (juvenile type)

code:
  v: prd2858
display:
  v: 2858 - Nephronophthisis - type 2 (infantile type)

code:
  v: prd2862
display:
  v: 2862 - Nephronophthisis - type 3 (adolescent type)

code:
  v: prd2870
display:
  v: 2870 - Nephronophthisis - type 4 (juvenile type)

code:
  v: prd2889
display:
  v: 2889 - Nephronophthisis - type 5

code:
  v: prd2891
display:
  v: 2891 - Nephronophthisis - type 6

code:
  v: prd2098
display:
  v: 2098 - Nephropathy due to aminoglycosides - histologically proven

code:
  v: prd2080
display:
  v: 2080 - Nephropathy due to aminoglycosides - no histology

code:
  v: prd2112
display:
  v: 2112 - Nephropathy due to amphotericin - histologically proven

code:
  v: prd2108
display:
  v: 2108 - Nephropathy due to amphotericin - no histology

code:
  v: prd2033
display:
  v: 2033 - Nephropathy due to analgesic drugs - histologically proven

code:
  v: prd2022
display:
  v: 2022 - Nephropathy due to analgesic drugs - no histology

code:
  v: prd2051
display:
  v: 2051 - Nephropathy due to ciclosporin - histologically proven

code:
  v: prd2046
display:
  v: 2046 - Nephropathy due to ciclosporin - no histology

code:
  v: prd2131
display:
  v: 2131 - Nephropathy due to cisplatin - histologically proven

code:
  v: prd2120
display:
  v: 2120 - Nephropathy due to cisplatin - no histology

code:
  v: prd2681
display:
  v: 2681 - Nephropathy due to eclampsia

code:
  v: prd2154
display:
  v: 2154 - Nephropathy due to lithium - histologically proven

code:
  v: prd2149
display:
  v: 2149 - Nephropathy due to lithium - no histology

code:
  v: prd3834
display:
  v: 3834 - Nephropathy due to pre-eclampsia

code:
  v: prd2079
display:
  v: 2079 - Nephropathy due to tacrolimus - histologically proven

code:
  v: prd2067
display:
  v: 2067 - Nephropathy due to tacrolimus - no histology

code:
  v: prd2288
display:
  v: 2288 - Nephropathy related to HIV - histologically proven

code:
  v: prd2274
display:
  v: 2274 - Nephropathy related to HIV - no histology

code:
  v: prd3615
display:
  v: 3615 - Nephrotic syndrome of childhood - no trial of steroids - no histology

code:
  v: prd3604
display:
  v: 3604 - Nephrotic syndrome of childhood - steroid resistant - no histology

code:
  v: prd1019
display:
  v: 1019 - Nephrotic syndrome of childhood - steroid sensitive - no histology

code:
  v: prd1799
display:
  v: 1799 - Obstructive nephropathy due to bladder cancer

code:
  v: prd1809
display:
  v: 1809 - Obstructive nephropathy due to other malignancies

code:
  v: prd1781
display:
  v: 1781 - Obstructive nephropathy due to prostate cancer

code:
  v: prd1775
display:
  v: 1775 - Obstructive nephropathy due to prostatic hypertrophy

code:
  v: prd1734
display:
  v: 1734 - Oligomeganephronia

code:
  v: prd2300
display:
  v: 2300 - Other specific infection

code:
  v: prd3063
display:
  v: 3063 - Phosphoribosyl pyrophosphate synthetase (PRPPS) superactivity

code:
  v: prd1455
display:
  v: 1455 - Polyarteritis nodosa

code:
  v: prd1687
display:
  v: 1687 - Posterior urethral valves

code:
  v: prd2901
display:
  v: 2901 - Primary Fanconi syndrome

code:
  v: prd1267
display:
  v: 1267 - Primary focal segmental glomerulosclerosis (FSGS)

code:
  v: prd3194
display:
  v: 3194 - Primary hyperoxaluria

code:
  v: prd3207
display:
  v: 3207 - Primary hyperoxaluria type I

code:
  v: prd3211
display:
  v: 3211 - Primary hyperoxaluria type II

code:
  v: prd3731
display:
  v: 3731 - Primary hyperoxaluria type III

code:
  v: prd1602
display:
  v: 1602 - Primary reflux nephropathy - sporadic

code:
  v: prd3000
display:
  v: 3000 - Primary renal tubular acidosis (RTA)

code:
  v: prd3016
display:
  v: 3016 - Proximal renal tubular acidosis (RTA) - type II

code:
  v: prd3141
display:
  v: 3141 - Pseudohypoaldosteronism type 1

code:
  v: prd3156
display:
  v: 3156 - Pseudohypoaldosteronism type 2 (Gordon syndrome)

code:
  v: prd2219
display:
  v: 2219 - Radiation nephritis

code:
  v: prd2226
display:
  v: 2226 - Renal / perinephric abscess

code:
  v: prd2509
display:
  v: 2509 - Renal amyloidosis

code:
  v: prd2469
display:
  v: 2469 - Renal arterial thrombosis / occlusion

code:
  v: prd2424
display:
  v: 2424 - Renal artery stenosis

code:
  v: prd3474
display:
  v: 3474 - Renal cell carcinoma - histologically proven

code:
  v: prd3658
display:
  v: 3658 - Renal coloboma syndrome

code:
  v: prd3627
display:
  v: 3627 - Renal cysts and diabetes syndrome

code:
  v: prd1641
display:
  v: 1641 - Renal dysplasia due to fetal ACE-inhibitor exposure

code:
  v: prd3691
display:
  v: 3691 - Renal failure

code:
  v: prd1747
display:
  v: 1747 - Renal papillary necrosis

code:
  v: prd3796
display:
  v: 3796 - Renal papillary necrosis caused by analgesics

code:
  v: prd3783
display:
  v: 3783 - Renal papillary necrosis caused by diabetes

code:
  v: prd3806
display:
  v: 3806 - Renal papillary necrosis caused by sickle cell

code:
  v: prd1976
display:
  v: 1976 - Renal sarcoidosis - histologically proven

code:
  v: prd1969
display:
  v: 1969 - Renal sarcoidosis - no histology

code:
  v: prd1536
display:
  v: 1536 - Renal scleroderma / systemic sclerosis - histologically proven

code:
  v: prd1527
display:
  v: 1527 - Renal scleroderma / systemic sclerosis - no histology

code:
  v: prd2235
display:
  v: 2235 - Renal tuberculosis

code:
  v: prd2476
display:
  v: 2476 - Renal vein thrombosis

code:
  v: prd3689
display:
  v: 3689 - Retroperitoneal fibrosis secondary to drugs

code:
  v: prd1821
display:
  v: 1821 - Retroperitoneal fibrosis secondary to malignancies

code:
  v: prd3670
display:
  v: 3670 - Retroperitoneal fibrosis secondary to peri-aortitis

code:
  v: prd3269
display:
  v: 3269 - Rubinstein-Taybi syndrome

code:
  v: prd2290
display:
  v: 2290 - Schistosomiasis

code:
  v: prd2702
display:
  v: 2702 - Sickle cell nephropathy - histologically proven

code:
  v: prd2699
display:
  v: 2699 - Sickle cell nephropathy - no histology

code:
  v: prd3517
display:
  v: 3517 - Single kidney identified in adulthood

code:
  v: prd1694
display:
  v: 1694 - Syndrome of agenesis of abdominal muscles - prune belly syndrome

code:
  v: prd1493
display:
  v: 1493 - Systemic lupus erythematosus / nephritis - histologically proven

code:
  v: prd1486
display:
  v: 1486 - Systemic lupus erythematosus / nephritis - no histology

code:
  v: prd1383
display:
  v: 1383 - Systemic vasculitis - ANCA negative - histologically proven

code:
  v: prd3847
display:
  v: 3847 - Systemic vasculitis - ANCA negative - no histology

code:
  v: prd3852
display:
  v: 3852 - Systemic vasculitis - ANCA positive - histologically proven

code:
  v: prd1396
display:
  v: 1396 - Systemic vasculitis - ANCA positive - no histology

code:
  v: prd2787
display:
  v: 2787 - Thin basement membrane disease

code:
  v: prd2634
display:
  v: 2634 - Thrombotic thrombocytopenic purpura (TTP)

code:
  v: prd3346
display:
  v: 3346 - Townes-Brocks syndrome

code:
  v: prd3488
display:
  v: 3488 - Transitional cell carcinoma - histologically proven

code:
  v: prd3276
display:
  v: 3276 - Tuberous sclerosis

code:
  v: prd2917
display:
  v: 2917 - Tubular disorder as part of inherited metabolic diseases

code:
  v: prd1897
display:
  v: 1897 - Tubulointerstitial nephritis - histologically proven

code:
  v: prd1884
display:
  v: 1884 - Tubulointerstitial nephritis - no histology

code:
  v: prd1930
display:
  v: 1930 - Tubulointerstitial nephritis associated with autoimmune disease - histologically proven

code:
  v: prd1924
display:
  v: 1924 - Tubulointerstitial nephritis associated with autoimmune disease - no histology

code:
  v: prd1953
display:
  v: 1953 - Tubulointerstitial nephritis with uveitis (TINU) - histologically proven

code:
  v: prd1948
display:
  v: 1948 - Tubulointerstitial nephritis with uveitis (TINU) - no histology

code:
  v: prd1878
display:
  v: 1878 - Uric acid urolithiasis

code:
  v: prd2827
display:
  v: 2827 - Uromodulin-associated nephropathy (familial juvenile hyperuricaemic nephropathy)

code:
  v: prd3282
display:
  v: 3282 - Von Hippel-Lindau disease

code:
  v: prd3333
display:
  v: 3333 - Williams syndrome

code:
  v: prd3490
display:
  v: 3490 - Wilms tumour - histologically proven

code:
  v: prd3248
display:
  v: 3248 - Xanthinuria

code:
  v: prd2261
display:
  v: 2261 - Xanthogranulomatous pyelonephritis