KIP Infrastructure
2.13.0 - ci-build

KIP Infrastructure, published by Sundhedsvæsenets Kvalitetsinstitut with Trifork Digital Health A/S. This guide is not an authorized publication; it is the continuous build for version 2.13.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/KIP-infrastructure/implementation-guide/ and changes regularly. See the Directory of published versions

ValueSet: ERA PRD Codes (Experimental)

Official URL: https://kip.rkkp.dk/fhir/ValueSet/PRDcodes Version: 2.13.0
Active as of 2024-01-10 Computable Name: PRDcodes

European Renal Association (ERA) Primary Renal Disease (PRD)

References

This value set is not used here; it may be used elsewhere (e.g. specifications and/or implementations that use this content)

Logical Definition (CLD)

  • Include these codes as defined in https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes version 📦2.13.0
    CodeDisplayDefinition
    prd25132513 - AA amyloid secondary to chronic inflammationAA amyloid secondary to chronic inflammation
    prd17681768 - Acquired obstructive nephropathy due to neurogenic bladderAcquired obstructive nephropathy due to neurogenic bladder
    prd17521752 - Acquired obstructive uropathy / nephropathy Acquired obstructive uropathy / nephropathy
    prd34423442 - Acute cortical necrosisAcute cortical necrosis
    prd33803380 - Acute kidney injuryAcute kidney injury
    prd34033403 - Acute kidney injury due to circulatory failureAcute kidney injury due to circulatory failure
    prd33983398 - Acute kidney injury due to hypovolaemia Acute kidney injury due to hypovolaemia
    prd34353435 - Acute kidney injury due to nephrotoxicityAcute kidney injury due to nephrotoxicity
    prd34263426 - Acute kidney injury due to rhabdomyolysisAcute kidney injury due to rhabdomyolysis
    prd34193419 - Acute kidney injury due to sepsisAcute kidney injury due to sepsis
    prd34573457 - Acute pyelonephritisAcute pyelonephritis
    prd21962196 - Acute urate nephropathy - histologically provenAcute urate nephropathy - histologically proven
    prd21832183 - Acute urate nephropathy - no histologyAcute urate nephropathy - no histology
    prd10031003 - Adult nephrotic syndrome - no histologyAdult nephrotic syndrome - no histology
    prd23922392 - Ageing kidney - no histologyAgeing kidney - no histology
    prd25212521 - AL amyloid secondary to plasma cell dyscrasiaAL amyloid secondary to plasma cell dyscrasia
    prd30713071 - Alagille syndromeAlagille syndrome
    prd27602760 - Alport syndrome - histologically provenAlport syndrome - histologically proven
    prd27562756 - Alport syndrome - no histologyAlport syndrome - no histology
    prd14721472 - Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - histologically provenAnti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - histologically proven
    prd14641464 - Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - no histologyAnti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - no histology
    prd31183118 - Apparent mineralocorticoid excessApparent mineralocorticoid excess
    prd19951995 - Aristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - histologically provenAristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - histologically proven
    prd19821982 - Aristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - no histologyAristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - no histology
    prd24482448 - Atheroembolic renal disease - histologically provenAtheroembolic renal disease - histologically proven
    prd24302430 - Atheroembolic renal disease - no histologyAtheroembolic renal disease - no histology
    prd26232623 - Atypical haemolytic uraemic syndrome (HUS) - diarrhoea negativeAtypical haemolytic uraemic syndrome (HUS) - diarrhoea negative
    prd27182718 - Autosomal dominant (AD) polycystic kidney diseaseAutosomal dominant (AD) polycystic kidney disease
    prd27252725 - Autosomal dominant (AD) polycystic kidney disease type IAutosomal dominant (AD) polycystic kidney disease type I
    prd27392739 - Autosomal dominant (AD) polycystic kidney disease type IIAutosomal dominant (AD) polycystic kidney disease type II
    prd27412741 - Autosomal recessive (AR) polycystic kidney diseaseAutosomal recessive (AR) polycystic kidney disease
    prd30853085 - Bartter syndromeBartter syndrome
    prd27732773 - Benign familial haematuriaBenign familial haematuria
    prd17101710 - Bladder exstrophyBladder exstrophy
    prd33223322 - Branchio-oto-renal syndromeBranchio-oto-renal syndrome
    prd18451845 - Calcium oxalate urolithiasisCalcium oxalate urolithiasis
    prd18321832 - Calculus nephropathy / urolithiasisCalculus nephropathy / urolithiasis
    prd24822482 - Cardiorenal syndromeCardiorenal syndrome
    prd23632363 - Chronic hypertensive nephropathy - histologically provenChronic hypertensive nephropathy - histologically proven
    prd23592359 - Chronic hypertensive nephropathy - no histologyChronic hypertensive nephropathy - no histology
    prd35643564 - Chronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - histologically provenChronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - histologically proven
    prd35553555 - Chronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - no histologyChronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - no histology
    prd35293529 - Chronic kidney disease (CKD) / chronic renal failure (CRF) caused by tumour nephrectomyChronic kidney disease (CKD) / chronic renal failure (CRF) caused by tumour nephrectomy
    prd35403540 - Chronic kidney disease (CKD) / chronic renal failure (CRF) due to donor nephrectomyChronic kidney disease (CKD) / chronic renal failure (CRF) due to donor nephrectomy
    prd35383538 - Chronic kidney disease (CKD) / chronic renal failure (CRF) due to traumatic loss of kidneyChronic kidney disease (CKD) / chronic renal failure (CRF) due to traumatic loss of kidney
    prd37083708 - Chronic renal failureChronic renal failure
    prd36433643 - Chronic renal failure due to systemic infectionChronic renal failure due to systemic infection
    prd22032203 - Chronic urate nephropathy - histologically provenChronic urate nephropathy - histologically proven
    prd36363636 - Chronic urate nephropathy - no histologyChronic urate nephropathy - no histology
    prd14401440 - Churg-Strauss syndrome - histologically provenChurg-Strauss syndrome - histologically proven
    prd14381438 - Churg-Strauss syndrome - no histologyChurg-Strauss syndrome - no histology
    prd16251625 - Congenital dysplasia / hypoplasiaCongenital dysplasia / hypoplasia
    prd26522652 - Congenital haemolytic uraemic syndromeCongenital haemolytic uraemic syndrome (HUS)
    prd10881088 - Congenital nephrotic syndrome (CNS) - congenital infectionCongenital nephrotic syndrome (CNS) - congenital infection
    prd10571057 - Congenital nephrotic syndrome (CNS) - diffuse mesangial sclerosisCongenital nephrotic syndrome (CNS) - diffuse mesangial sclerosis
    prd10421042 - Congenital nephrotic syndrome (CNS) - Finnish type - histologically provenCongenital nephrotic syndrome (CNS) - Finnish type - histologically proven
    prd10351035 - Congenital nephrotic syndrome (CNS) - Finnish type - no histologyCongenital nephrotic syndrome (CNS) - Finnish type - no histology
    prd10611061 - Congenital nephrotic syndrome (CNS) - focal segmental glomerulosclerosisCongenital nephrotic syndrome (CNS) - focal segmental glomerulosclerosis (FSGS)
    prd10261026 - Congenital nephrotic syndrome - no histologyCongenital nephrotic syndrome (CNS) - no histology
    prd17061706 - Congenital neurogenic bladderCongenital neurogenic bladder
    prd16601660 - Congenital pelvi-ureteric junction obstructionCongenital pelvi-ureteric junction obstruction
    prd16731673 - Congenital vesico-ureteric junction obstructionCongenital vesico-ureteric junction obstruction
    prd15701570 - Cryoglobulinaemia secondary to hepatitis C - histologically provenCryoglobulinaemia secondary to hepatitis C - histologically proven
    prd15621562 - Cryoglobulinaemia secondary to hepatitis C - no histologyCryoglobulinaemia secondary to hepatitis C - no histology
    prd15911591 - Cryoglobulinaemia secondary to systemic disease - histologically provenCryoglobulinaemia secondary to systemic disease - histologically proven
    prd15891589 - Cryoglobulinaemia secondary to systemic disease - no histologyCryoglobulinaemia secondary to systemic disease - no histology
    prd27942794 - Cystic kidney diseaseCystic kidney disease
    prd29642964 - CystinosisCystinosis
    prd29552955 - CystinuriaCystinuria
    prd29292929 - Dent diseaseDent disease
    prd10741074 - Denys-Drash syndromeDenys-Drash syndrome
    prd23282328 - Diabetic nephropathy in type I diabetes - histologically provenDiabetic nephropathy in type I diabetes - histologically proven
    prd23162316 - Diabetic nephropathy in type I diabetes - no histologyDiabetic nephropathy in type I diabetes - no histology
    prd23442344 - Diabetic nephropathy in type II diabetes - histologically provenDiabetic nephropathy in type II diabetes - histologically proven
    prd23372337 - Diabetic nephropathy in type II diabetes - no histologyDiabetic nephropathy in type II diabetes - no histology
    prd13311331 - Diffuse endocapillary glomerulonephritisDiffuse endocapillary glomerulonephritis
    prd30283028 - Distal renal tubular acidosis - type IDistal renal tubular acidosis (RTA) - type I
    prd30373037 - Distal renal tubular acidosis with sensorineural deafness - gene mutationsDistal renal tubular acidosis with sensorineural deafness - gene mutations
    prd20052005 - Drug-induced tubulointerstitial nephritis - no histologyDrug-induced tubulointerstitial nephritis - no histology
    prd20142014 - Drug-induced tubulointerstitial nephritis - histologically provenDrug-induced tubulointerstitial nephritis - histologically proven
    prd18501850 - Enteric hyperoxaluriaEnteric hyperoxaluria
    prd15581558 - Essential mixed cryoglobulinaemia - histologically provenEssential mixed cryoglobulinaemia - histologically proven
    prd15431543 - Essential mixed cryoglobulinaemia - no histologyEssential mixed cryoglobulinaemia - no histology
    prd32303230 - Fabry disease - histologically provenFabry disease - histologically proven
    prd32243224 - Fabry disease - no histologyFabry disease - no histology
    prd25452545 - Familial amyloid secondary to protein mutations - histologically provenFamilial amyloid secondary to protein mutations - histologically proven
    prd25322532 - Familial amyloid secondary to protein mutations - no histologyFamilial amyloid secondary to protein mutations - no histology
    prd13081308 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - histologically provenFamilial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - histologically proven
    prd12981298 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - no histologyFamilial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - no histology
    prd12801280 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - histologically provenFamilial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - histologically proven
    prd12791279 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - no histologyFamilial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - no histology
    prd26682668 - Familial haemolytic uraemic syndrome (HUS)Familial haemolytic uraemic syndrome (HUS)
    prd31733173 - Familial hypercalciuric hypocalcaemiaFamilial hypercalciuric hypocalcaemia
    prd31603160 - Familial hypocalciuric hypercalcaemiaFamilial hypocalciuric hypercalcaemia
    prd31873187 - Familial hypomagnesaemiaFamilial hypomagnesaemia
    prd11441144 - Familial IgA nephropathy - histologically provenFamilial IgA nephropathy - histologically proven
    prd11371137 - Familial IgA nephropathy - no histologyFamilial IgA nephropathy - no histology
    prd19111911 - Familial interstitial nephropathy - histologically provenFamilial interstitial nephropathy - histologically proven
    prd19071907 - Familial interstitial nephropathy - no histologyFamilial interstitial nephropathy - no histology
    prd33793379 - Familial nephropathyFamilial nephropathy
    prd16181618 - Familial reflux nephropathyFamilial reflux nephropathy
    prd26752675 - Familial thrombotic thrombocytopenic purpura(2675)Familial thrombotic thrombocytopenic purpura (TTP)
    prd25662566 - Familial AA amyloid secondary to familial Mediterranean fever / TRAPS (Hibernian fever) - histologically provenFamilial AA amyloid secondary to familial Mediterranean fever / TRAPS (Hibernian fever) - histologically proven
    prd25502550 - Familial AA amyloid secondary to familial Mediterranean fever / TRAPS (Hibernian fever) - no histologyFamilial AA amyloid secondary to familial Mediterranean fever / TRAPS (Hibernian fever) - no histology
    prd24532453 - Fibromuscular dysplasia of renal arteryFibromuscular dysplasia of renal artery
    prd13541354 - Focal and segmental proliferative glomerulonephritisFocal and segmental proliferative glomerulonephritis
    prd37543754 - Focal segmental glomerulosclerosis (FSGS) secondary to HIV Focal segmental glomerulosclerosis (FSGS) secondary to HIV
    prd37653765 - Focal segmental glomerulosclerosis (FSGS) secondary to lithium Focal segmental glomerulosclerosis (FSGS) secondary to lithium
    prd13201320 - Focal segmental glomerulosclerosis (FSGS) secondary to obesity - histologically provenFocal segmental glomerulosclerosis (FSGS) secondary to obesity - histologically proven
    prd13121312 - Focal segmental glomerulosclerosis (FSGS) secondary to obesity - no histologyFocal segmental glomerulosclerosis (FSGS) secondary to obesity - no histology
    prd37773777 - Focal segmental glomerulosclerosis secondary to sickle cellFocal segmental glomerulosclerosis (FSGS) secondary to sickle cell
    prd33143314 - Frasier syndromeFrasier syndrome
    prd30923092 - Gitelman syndromeGitelman syndrome
    prd16561656 - Glomerulocystic diseaseGlomerulocystic disease
    prd13771377 - Glomerulonephritis - histologically indeterminateGlomerulonephritis - histologically indeterminate
    prd37493749 - Glomerulonephritis - no histologyGlomerulonephritis - no histology
    prd13651365 - Glomerulonephritis - secondary to systemic diseaseGlomerulonephritis - secondary to systemic disease
    prd31253125 - Glucocorticoid suppressible hyperaldosteronismGlucocorticoid suppressible hyperaldosteronism
    prd14171417 - Granulomatosis with polyangiitis - histologically provenGranulomatosis with polyangiitis - histologically proven
    prd14011401 - Granulomatosis with polyangiitis - no histologyGranulomatosis with polyangiitis - no histology
    prd35723572 - Haematuria and proteinuria - no histologyHaematuria and proteinuria - no histology
    prd26102610 - Haemolytic uraemic syndrome (HUS) - diarrhoea associatedHaemolytic uraemic syndrome (HUS) - diarrhoea associated
    prd26472647 - Haemolytic uraemic syndrome (HUS) secondary to systemic diseaseHaemolytic uraemic syndrome (HUS) secondary to systemic disease
    prd22572257 - Hantavirus nephropathyHantavirus nephropathy
    prd15151515 - Henoch-Schönlein purpura / nephritis - histologically provenHenoch-Schönlein purpura / nephritis - histologically proven
    prd15041504 - Henoch-Schönlein purpura / nephritis - no histologyHenoch-Schönlein purpura / nephritis - no histology
    prd24952495 - Hepatorenal syndromeHepatorenal syndrome
    prd33053305 - Horse-shoe kidneyHorse-shoe kidney
    prd36623662 - Hypercalcaemic nephropathyHypercalcaemic nephropathy
    prd29932993 - Hypophosphataemic rickets autosomal recessive (AR)Hypophosphataemic rickets autosomal recessive (AR)
    prd29862986 - Hypophosphataemic rickets X-linked (XL)Hypophosphataemic rickets X-linked (XL)
    prd12511251 - Idiopathic rapidly progressive (crescentic) glomerulonephritisIdiopathic rapidly progressive (crescentic) glomerulonephritis
    prd18131813 - Idiopathic retroperitoneal fibrosisIdiopathic retroperitoneal fibrosis
    prd11281128 - IgA nephropathy - histologically provenIgA nephropathy - histologically proven
    prd11161116 - IgA nephropathy - no histologyIgA nephropathy - no histology
    prd11631163 - IgA nephropathy secondary to liver cirrhosis - histologically provenIgA nephropathy secondary to liver cirrhosis - histologically proven
    prd11591159 - IgA nephropathy secondary to liver cirrhosis - no histologyIgA nephropathy secondary to liver cirrhosis - no histology
    prd11711171 - IgM - associated nephropathyIgM - associated nephropathy
    prd26062606 - Immunotactoid / fibrillary nephropathyImmunotactoid / fibrillary nephropathy
    prd38233823 - Infiltration by lymphoma - histologically provenInfiltration by lymphoma - histologically proven
    prd31393139 - Inherited / genetic diabetes mellitus type IIInherited / genetic diabetes mellitus type II
    prd29402940 - Inherited aminoaciduriaInherited aminoaciduria
    prd29722972 - Inherited renal glycosuriaInherited renal glycosuria
    prd24072407 - Ischaemic nephropathy - no histologyIschaemic nephropathy - no histology
    prd24112411 - Ischaemic nephropathy / microvascular disease - histologically provenIschaemic nephropathy / microvascular disease - histologically proven
    prd37123712 - Isolated haematuria - no histologyIsolated haematuria - no histology
    prd37203720 - Isolated proteinuria - no histologyIsolated proteinuria - no histology
    prd38103810 - Kidney stones due to ARPT deficiencyKidney stones due to ARPT deficiency
    prd34613461 - Kidney tumourKidney tumour
    prd33513351 - Lawrence-Moon-Biedl / Bardet-Biedl syndromeLawrence-Moon-Biedl / Bardet-Biedl syndrome
    prd21772177 - Lead induced nephropathy - histologically provenLead induced nephropathy - histologically proven
    prd21652165 - Lead induced nephropathy - no histologyLead induced nephropathy - no histology
    prd22422242 - LeptospirosisLeptospirosis
    prd30593059 - Lesch Nyhan syndrome - hypoxanthine guanine phosphoribosyl transferase deficiencyLesch Nyhan syndrome - hypoxanthine guanine phosphoribosyl transferase deficiency
    prd31023102 - Liddle syndromeLiddle syndrome
    prd25972597 - Light chain deposition diseaseLight chain deposition disease
    prd29382938 - Lowe syndrome (oculocerebrorenal syndrome)Lowe syndrome (oculocerebrorenal syndrome)
    prd18661866 - Magnesium ammonium phosphate (struvite) urolithiasisMagnesium ammonium phosphate (struvite) urolithiasis
    prd23852385 - Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - histologically provenMalignant hypertensive nephropathy / accelerated hypertensive nephropathy - histologically proven
    prd23712371 - Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - no histologyMalignant hypertensive nephropathy / accelerated hypertensive nephropathy - no histology
    prd28042804 - Medullary cystic kidney disease type IMedullary cystic kidney disease type I
    prd28152815 - Medullary cystic kidney disease type IIMedullary cystic kidney disease type II
    prd32953295 - Medullary sponge kidneysMedullary sponge kidneys
    prd17231723 - Megacystis-megaureterMegacystis-megaureter
    prd12051205 - Membranous nephropathy - drug inducedMembranous nephropathy - drug induced
    prd11851185 - Membranous nephropathy - idiopathicMembranous nephropathy - idiopathic
    prd12141214 - Membranous nephropathy - infection associatedMembranous nephropathy - infection associated
    prd11921192 - Membranous nephropathy - malignancy associatedMembranous nephropathy - malignancy associated
    prd13491349 - Mesangial proliferative glomerulonephritis Mesangial proliferative glomerulonephritis
    prd12221222 - Mesangiocapillary glomerulonephritis type 1Mesangiocapillary glomerulonephritis type 1
    prd12331233 - Mesangiocapillary glomerulonephritis type 2 (dense deposit disease)Mesangiocapillary glomerulonephritis type 2 (dense deposit disease)
    prd12461246 - Mesangiocapillary glomerulonephritis type 3Mesangiocapillary glomerulonephritis type 3
    prd35013501 - Mesoblastic nephroma - histologically provenMesoblastic nephroma - histologically proven
    prd14291429 - Microscopic polyangiitis - histologically provenMicroscopic polyangiitis - histologically proven
    prd11001100 - Minimal change nephropathy - histologically provenMinimal change nephropathy - histologically proven
    prd10901090 - Minimal change nephropathy - no histologyMinimal change nephropathy - no histology
    prd33673367 - Mitochondrial cytopathyMitochondrial cytopathy
    prd16391639 - Multicystic dysplastic kidneysMulticystic dysplastic kidneys
    prd25842584 - Myeloma cast nephropathy - histologically provenMyeloma cast nephropathy - histologically proven
    prd25782578 - Myeloma kidney - no histologyMyeloma kidney - no histology
    prd32533253 - Nail-patella syndromeNail-patella syndrome
    prd30443044 - Nephrogenic diabetes insipidusNephrogenic diabetes insipidus
    prd28362836 - NephronophthisisNephronophthisis
    prd28432843 - Nephronophthisis - type 1 (juvenile type)Nephronophthisis - type 1 (juvenile type)
    prd28582858 - Nephronophthisis - type 2 (infantile type)Nephronophthisis - type 2 (infantile type)
    prd28622862 - Nephronophthisis - type 3 (adolescent type)Nephronophthisis - type 3 (adolescent type)
    prd28702870 - Nephronophthisis - type 4 (juvenile type)Nephronophthisis - type 4 (juvenile type)
    prd28892889 - Nephronophthisis - type 5Nephronophthisis - type 5
    prd28912891 - Nephronophthisis - type 6Nephronophthisis - type 6
    prd20982098 - Nephropathy due to aminoglycosides - histologically provenNephropathy due to aminoglycosides - histologically proven
    prd20802080 - Nephropathy due to aminoglycosides - no histologyNephropathy due to aminoglycosides - no histology
    prd21122112 - Nephropathy due to amphotericin - histologically provenNephropathy due to amphotericin - histologically proven
    prd21082108 - Nephropathy due to amphotericin - no histologyNephropathy due to amphotericin - no histology
    prd20332033 - Nephropathy due to analgesic drugs - histologically provenNephropathy due to analgesic drugs - histologically proven
    prd20222022 - Nephropathy due to analgesic drugs - no histologyNephropathy due to analgesic drugs - no histology
    prd20512051 - Nephropathy due to ciclosporin - histologically provenNephropathy due to ciclosporin - histologically proven
    prd20462046 - Nephropathy due to ciclosporin - no histologyNephropathy due to ciclosporin - no histology
    prd21312131 - Nephropathy due to cisplatin - histologically provenNephropathy due to cisplatin - histologically proven
    prd21202120 - Nephropathy due to cisplatin - no histologyNephropathy due to cisplatin - no histology
    prd26812681 - Nephropathy due to eclampsiaNephropathy due to eclampsia
    prd21542154 - Nephropathy due to lithium - histologically provenNephropathy due to lithium - histologically proven
    prd21492149 - Nephropathy due to lithium - no histologyNephropathy due to lithium - no histology
    prd38343834 - Nephropathy due to pre-eclampsiaNephropathy due to pre-eclampsia
    prd20792079 - Nephropathy due to tacrolimus - histologically provenNephropathy due to tacrolimus - histologically proven
    prd20672067 - Nephropathy due to tacrolimus - no histologyNephropathy due to tacrolimus - no histology
    prd22882288 - Nephropathy related to HIV - histologically provenNephropathy related to HIV - histologically proven
    prd22742274 - Nephropathy related to HIV - no histologyNephropathy related to HIV - no histology
    prd36153615 - Nephrotic syndrome of childhood - no trial of steroids - no histologyNephrotic syndrome of childhood - no trial of steroids - no histology
    prd36043604 - Nephrotic syndrome of childhood - steroid resistant - no histologyNephrotic syndrome of childhood - steroid resistant - no histology
    prd10191019 - Nephrotic syndrome of childhood - steroid sensitive - no histologyNephrotic syndrome of childhood - steroid sensitive - no histology
    prd17991799 - Obstructive nephropathy due to bladder cancerObstructive nephropathy due to bladder cancer
    prd18091809 - Obstructive nephropathy due to other malignanciesObstructive nephropathy due to other malignancies
    prd17811781 - Obstructive nephropathy due to prostate cancerObstructive nephropathy due to prostate cancer
    prd17751775 - Obstructive nephropathy due to prostatic hypertrophyObstructive nephropathy due to prostatic hypertrophy
    prd17341734 - OligomeganephroniaOligomeganephronia
    prd23002300 - Other specific infectionOther specific infection
    prd30633063 - Phosphoribosyl pyrophosphate synthetase (PRPPS) superactivityPhosphoribosyl pyrophosphate synthetase (PRPPS) superactivity
    prd14551455 - Polyarteritis nodosaPolyarteritis nodosa
    prd16871687 - Posterior urethral valvesPosterior urethral valves
    prd29012901 - Primary Fanconi syndromePrimary Fanconi syndrome
    prd12671267 - Primary focal segmental glomerulosclerosis (FSGS)Primary focal segmental glomerulosclerosis (FSGS)
    prd31943194 - Primary hyperoxaluriaPrimary hyperoxaluria
    prd32073207 - Primary hyperoxaluria type IPrimary hyperoxaluria type I
    prd32113211 - Primary hyperoxaluria type IIPrimary hyperoxaluria type II
    prd37313731 - Primary hyperoxaluria type IIIPrimary hyperoxaluria type III
    prd16021602 - Primary reflux nephropathy - sporadicPrimary reflux nephropathy - sporadic
    prd30003000 - Primary renal tubular acidosis (RTA)Primary renal tubular acidosis (RTA)
    prd30163016 - Proximal renal tubular acidosis (RTA) - type IIProximal renal tubular acidosis (RTA) - type II
    prd31413141 - Pseudohypoaldosteronism type 1Pseudohypoaldosteronism type 1
    prd31563156 - Pseudohypoaldosteronism type 2 (Gordon syndrome)Pseudohypoaldosteronism type 2 (Gordon syndrome)
    prd22192219 - Radiation nephritisRadiation nephritis
    prd22262226 - Renal / perinephric abscessRenal / perinephric abscess
    prd25092509 - Renal amyloidosisRenal amyloidosis
    prd24692469 - Renal arterial thrombosis / occlusionRenal arterial thrombosis / occlusion
    prd24242424 - Renal artery stenosisRenal artery stenosis
    prd34743474 - Renal cell carcinoma - histologically provenRenal cell carcinoma - histologically proven
    prd36583658 - Renal coloboma syndromeRenal coloboma syndrome
    prd36273627 - Renal cysts and diabetes syndromeRenal cysts and diabetes syndrome
    prd16411641 - Renal dysplasia due to fetal ACE-inhibitor exposureRenal dysplasia due to fetal ACE-inhibitor exposure
    prd36913691 - Renal failureRenal failure
    prd17471747 - Renal papillary necrosisRenal papillary necrosis
    prd37963796 - Renal papillary necrosis caused by analgesicsRenal papillary necrosis caused by analgesics
    prd37833783 - Renal papillary necrosis caused by diabetesRenal papillary necrosis caused by diabetes
    prd38063806 - Renal papillary necrosis caused by sickle cellRenal papillary necrosis caused by sickle cell
    prd19761976 - Renal sarcoidosis - histologically provenRenal sarcoidosis - histologically proven
    prd19691969 - Renal sarcoidosis - no histologyRenal sarcoidosis - no histology
    prd15361536 - Renal scleroderma / systemic sclerosis - histologically provenRenal scleroderma / systemic sclerosis - histologically proven
    prd15271527 - Renal scleroderma / systemic sclerosis - no histologyRenal scleroderma / systemic sclerosis - no histology
    prd22352235 - Renal tuberculosisRenal tuberculosis
    prd24762476 - Renal vein thrombosisRenal vein thrombosis
    prd36893689 - Retroperitoneal fibrosis secondary to drugsRetroperitoneal fibrosis secondary to drugs
    prd18211821 - Retroperitoneal fibrosis secondary to malignanciesRetroperitoneal fibrosis secondary to malignancies
    prd36703670 - Retroperitoneal fibrosis secondary to peri-aortitisRetroperitoneal fibrosis secondary to peri-aortitis
    prd32693269 - Rubinstein-Taybi syndromeRubinstein-Taybi syndrome
    prd22902290 - SchistosomiasisSchistosomiasis
    prd27022702 - Sickle cell nephropathy - histologically provenSickle cell nephropathy - histologically proven
    prd26992699 - Sickle cell nephropathy - no histologySickle cell nephropathy - no histology
    prd35173517 - Single kidney identified in adulthoodSingle kidney identified in adulthood
    prd16941694 - Syndrome of agenesis of abdominal muscles - prune belly syndromeSyndrome of agenesis of abdominal muscles - prune belly syndrome
    prd14931493 - Systemic lupus erythematosus / nephritis - histologically provenSystemic lupus erythematosus / nephritis - histologically proven
    prd14861486 - Systemic lupus erythematosus / nephritis - no histologySystemic lupus erythematosus / nephritis - no histology
    prd13831383 - Systemic vasculitis - ANCA negative - histologically provenSystemic vasculitis - ANCA negative - histologically proven
    prd38473847 - Systemic vasculitis - ANCA negative - no histologySystemic vasculitis - ANCA negative - no histology
    prd38523852 - Systemic vasculitis - ANCA positive - histologically provenSystemic vasculitis - ANCA positive - histologically proven
    prd13961396 - Systemic vasculitis - ANCA positive - no histologySystemic vasculitis - ANCA positive - no histology
    prd27872787 - Thin basement membrane diseaseThin basement membrane disease
    prd26342634 - Thrombotic thrombocytopenic purpura (TTP)Thrombotic thrombocytopenic purpura (TTP)
    prd33463346 - Townes-Brocks syndromeTownes-Brocks syndrome
    prd34883488 - Transitional cell carcinoma - histologically provenTransitional cell carcinoma - histologically proven
    prd32763276 - Tuberous sclerosisTuberous sclerosis
    prd29172917 - Tubular disorder as part of inherited metabolic diseasesTubular disorder as part of inherited metabolic diseases
    prd18971897 - Tubulointerstitial nephritis - histologically provenTubulointerstitial nephritis - histologically proven
    prd18841884 - Tubulointerstitial nephritis - no histologyTubulointerstitial nephritis - no histology
    prd19301930 - Tubulointerstitial nephritis associated with autoimmune disease - histologically provenTubulointerstitial nephritis associated with autoimmune disease - histologically proven
    prd19241924 - Tubulointerstitial nephritis associated with autoimmune disease - no histologyTubulointerstitial nephritis associated with autoimmune disease - no histology
    prd19531953 - Tubulointerstitial nephritis with uveitis (TINU) - histologically provenTubulointerstitial nephritis with uveitis (TINU) - histologically proven
    prd19481948 - Tubulointerstitial nephritis with uveitis (TINU) - no histologyTubulointerstitial nephritis with uveitis (TINU) - no histology
    prd18781878 - Uric acid urolithiasisUric acid urolithiasis
    prd28272827 - Uromodulin-associated nephropathy (familial juvenile hyperuricaemic nephropathy)Uromodulin-associated nephropathy (familial juvenile hyperuricaemic nephropathy)
    prd32823282 - Von Hippel-Lindau diseaseVon Hippel-Lindau disease
    prd33333333 - Williams syndromeWilliams syndrome
    prd34903490 - Wilms tumour - histologically provenWilms tumour - histologically proven
    prd32483248 - XanthinuriaXanthinuria
    prd22612261 - Xanthogranulomatous pyelonephritisXanthogranulomatous pyelonephritis

 

Expansion

Expansion performed internally based on codesystem ERA PRD Codes v2.13.0 (CodeSystem)

This value set contains 284 concepts

SystemCodeDisplay (en)JSONXML
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd25132513 - AA amyloid secondary to chronic inflammation
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd17681768 - Acquired obstructive nephropathy due to neurogenic bladder
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd17521752 - Acquired obstructive uropathy / nephropathy
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd34423442 - Acute cortical necrosis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd33803380 - Acute kidney injury
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd34033403 - Acute kidney injury due to circulatory failure
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd33983398 - Acute kidney injury due to hypovolaemia
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd34353435 - Acute kidney injury due to nephrotoxicity
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd34263426 - Acute kidney injury due to rhabdomyolysis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd34193419 - Acute kidney injury due to sepsis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd34573457 - Acute pyelonephritis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd21962196 - Acute urate nephropathy - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd21832183 - Acute urate nephropathy - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd10031003 - Adult nephrotic syndrome - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd23922392 - Ageing kidney - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd25212521 - AL amyloid secondary to plasma cell dyscrasia
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd30713071 - Alagille syndrome
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd27602760 - Alport syndrome - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd27562756 - Alport syndrome - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd14721472 - Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd14641464 - Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd31183118 - Apparent mineralocorticoid excess
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd19951995 - Aristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd19821982 - Aristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd24482448 - Atheroembolic renal disease - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd24302430 - Atheroembolic renal disease - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd26232623 - Atypical haemolytic uraemic syndrome (HUS) - diarrhoea negative
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd27182718 - Autosomal dominant (AD) polycystic kidney disease
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd27252725 - Autosomal dominant (AD) polycystic kidney disease type I
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd27392739 - Autosomal dominant (AD) polycystic kidney disease type II
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd27412741 - Autosomal recessive (AR) polycystic kidney disease
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd30853085 - Bartter syndrome
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd27732773 - Benign familial haematuria
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd17101710 - Bladder exstrophy
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd33223322 - Branchio-oto-renal syndrome
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd18451845 - Calcium oxalate urolithiasis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd18321832 - Calculus nephropathy / urolithiasis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd24822482 - Cardiorenal syndrome
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd23632363 - Chronic hypertensive nephropathy - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd23592359 - Chronic hypertensive nephropathy - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd35643564 - Chronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd35553555 - Chronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd35293529 - Chronic kidney disease (CKD) / chronic renal failure (CRF) caused by tumour nephrectomy
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd35403540 - Chronic kidney disease (CKD) / chronic renal failure (CRF) due to donor nephrectomy
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd35383538 - Chronic kidney disease (CKD) / chronic renal failure (CRF) due to traumatic loss of kidney
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd37083708 - Chronic renal failure
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd36433643 - Chronic renal failure due to systemic infection
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd22032203 - Chronic urate nephropathy - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd36363636 - Chronic urate nephropathy - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd14401440 - Churg-Strauss syndrome - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd14381438 - Churg-Strauss syndrome - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd16251625 - Congenital dysplasia / hypoplasia
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd26522652 - Congenital haemolytic uraemic syndrome
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd10881088 - Congenital nephrotic syndrome (CNS) - congenital infection
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd10571057 - Congenital nephrotic syndrome (CNS) - diffuse mesangial sclerosis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd10421042 - Congenital nephrotic syndrome (CNS) - Finnish type - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd10351035 - Congenital nephrotic syndrome (CNS) - Finnish type - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd10611061 - Congenital nephrotic syndrome (CNS) - focal segmental glomerulosclerosis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd10261026 - Congenital nephrotic syndrome - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd17061706 - Congenital neurogenic bladder
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd16601660 - Congenital pelvi-ureteric junction obstruction
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd16731673 - Congenital vesico-ureteric junction obstruction
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd15701570 - Cryoglobulinaemia secondary to hepatitis C - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd15621562 - Cryoglobulinaemia secondary to hepatitis C - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd15911591 - Cryoglobulinaemia secondary to systemic disease - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd15891589 - Cryoglobulinaemia secondary to systemic disease - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd27942794 - Cystic kidney disease
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd29642964 - Cystinosis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd29552955 - Cystinuria
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd29292929 - Dent disease
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd10741074 - Denys-Drash syndrome
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd23282328 - Diabetic nephropathy in type I diabetes - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd23162316 - Diabetic nephropathy in type I diabetes - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd23442344 - Diabetic nephropathy in type II diabetes - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd23372337 - Diabetic nephropathy in type II diabetes - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd13311331 - Diffuse endocapillary glomerulonephritis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd30283028 - Distal renal tubular acidosis - type I
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd30373037 - Distal renal tubular acidosis with sensorineural deafness - gene mutations
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd20052005 - Drug-induced tubulointerstitial nephritis - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd20142014 - Drug-induced tubulointerstitial nephritis - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd18501850 - Enteric hyperoxaluria
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd15581558 - Essential mixed cryoglobulinaemia - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd15431543 - Essential mixed cryoglobulinaemia - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd32303230 - Fabry disease - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd32243224 - Fabry disease - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd25452545 - Familial amyloid secondary to protein mutations - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd25322532 - Familial amyloid secondary to protein mutations - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd13081308 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd12981298 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd12801280 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd12791279 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd26682668 - Familial haemolytic uraemic syndrome (HUS)
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd31733173 - Familial hypercalciuric hypocalcaemia
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd31603160 - Familial hypocalciuric hypercalcaemia
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd31873187 - Familial hypomagnesaemia
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd11441144 - Familial IgA nephropathy - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd11371137 - Familial IgA nephropathy - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd19111911 - Familial interstitial nephropathy - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd19071907 - Familial interstitial nephropathy - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd33793379 - Familial nephropathy
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd16181618 - Familial reflux nephropathy
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd26752675 - Familial thrombotic thrombocytopenic purpura(2675)
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd25662566 - Familial AA amyloid secondary to familial Mediterranean fever / TRAPS (Hibernian fever) - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd25502550 - Familial AA amyloid secondary to familial Mediterranean fever / TRAPS (Hibernian fever) - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd24532453 - Fibromuscular dysplasia of renal artery
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd13541354 - Focal and segmental proliferative glomerulonephritis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd37543754 - Focal segmental glomerulosclerosis (FSGS) secondary to HIV
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd37653765 - Focal segmental glomerulosclerosis (FSGS) secondary to lithium
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd13201320 - Focal segmental glomerulosclerosis (FSGS) secondary to obesity - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd13121312 - Focal segmental glomerulosclerosis (FSGS) secondary to obesity - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd37773777 - Focal segmental glomerulosclerosis secondary to sickle cell
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd33143314 - Frasier syndrome
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd30923092 - Gitelman syndrome
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd16561656 - Glomerulocystic disease
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd13771377 - Glomerulonephritis - histologically indeterminate
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd37493749 - Glomerulonephritis - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd13651365 - Glomerulonephritis - secondary to systemic disease
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd31253125 - Glucocorticoid suppressible hyperaldosteronism
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd14171417 - Granulomatosis with polyangiitis - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd14011401 - Granulomatosis with polyangiitis - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd35723572 - Haematuria and proteinuria - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd26102610 - Haemolytic uraemic syndrome (HUS) - diarrhoea associated
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd26472647 - Haemolytic uraemic syndrome (HUS) secondary to systemic disease
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd22572257 - Hantavirus nephropathy
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd15151515 - Henoch-Schönlein purpura / nephritis - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd15041504 - Henoch-Schönlein purpura / nephritis - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd24952495 - Hepatorenal syndrome
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd33053305 - Horse-shoe kidney
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd36623662 - Hypercalcaemic nephropathy
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd29932993 - Hypophosphataemic rickets autosomal recessive (AR)
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd29862986 - Hypophosphataemic rickets X-linked (XL)
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd12511251 - Idiopathic rapidly progressive (crescentic) glomerulonephritis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd18131813 - Idiopathic retroperitoneal fibrosis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd11281128 - IgA nephropathy - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd11161116 - IgA nephropathy - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd11631163 - IgA nephropathy secondary to liver cirrhosis - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd11591159 - IgA nephropathy secondary to liver cirrhosis - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd11711171 - IgM - associated nephropathy
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd26062606 - Immunotactoid / fibrillary nephropathy
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd38233823 - Infiltration by lymphoma - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd31393139 - Inherited / genetic diabetes mellitus type II
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd29402940 - Inherited aminoaciduria
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd29722972 - Inherited renal glycosuria
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd24072407 - Ischaemic nephropathy - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd24112411 - Ischaemic nephropathy / microvascular disease - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd37123712 - Isolated haematuria - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd37203720 - Isolated proteinuria - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd38103810 - Kidney stones due to ARPT deficiency
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd34613461 - Kidney tumour
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd33513351 - Lawrence-Moon-Biedl / Bardet-Biedl syndrome
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd21772177 - Lead induced nephropathy - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd21652165 - Lead induced nephropathy - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd22422242 - Leptospirosis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd30593059 - Lesch Nyhan syndrome - hypoxanthine guanine phosphoribosyl transferase deficiency
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd31023102 - Liddle syndrome
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd25972597 - Light chain deposition disease
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd29382938 - Lowe syndrome (oculocerebrorenal syndrome)
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd18661866 - Magnesium ammonium phosphate (struvite) urolithiasis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd23852385 - Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd23712371 - Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd28042804 - Medullary cystic kidney disease type I
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd28152815 - Medullary cystic kidney disease type II
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd32953295 - Medullary sponge kidneys
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd17231723 - Megacystis-megaureter
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd12051205 - Membranous nephropathy - drug induced
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd11851185 - Membranous nephropathy - idiopathic
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd12141214 - Membranous nephropathy - infection associated
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd11921192 - Membranous nephropathy - malignancy associated
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd13491349 - Mesangial proliferative glomerulonephritis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd12221222 - Mesangiocapillary glomerulonephritis type 1
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd12331233 - Mesangiocapillary glomerulonephritis type 2 (dense deposit disease)
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd12461246 - Mesangiocapillary glomerulonephritis type 3
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd35013501 - Mesoblastic nephroma - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd14291429 - Microscopic polyangiitis - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd11001100 - Minimal change nephropathy - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd10901090 - Minimal change nephropathy - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd33673367 - Mitochondrial cytopathy
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd16391639 - Multicystic dysplastic kidneys
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd25842584 - Myeloma cast nephropathy - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd25782578 - Myeloma kidney - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd32533253 - Nail-patella syndrome
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd30443044 - Nephrogenic diabetes insipidus
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd28362836 - Nephronophthisis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd28432843 - Nephronophthisis - type 1 (juvenile type)
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd28582858 - Nephronophthisis - type 2 (infantile type)
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd28622862 - Nephronophthisis - type 3 (adolescent type)
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd28702870 - Nephronophthisis - type 4 (juvenile type)
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd28892889 - Nephronophthisis - type 5
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd28912891 - Nephronophthisis - type 6
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd20982098 - Nephropathy due to aminoglycosides - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd20802080 - Nephropathy due to aminoglycosides - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd21122112 - Nephropathy due to amphotericin - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd21082108 - Nephropathy due to amphotericin - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd20332033 - Nephropathy due to analgesic drugs - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd20222022 - Nephropathy due to analgesic drugs - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd20512051 - Nephropathy due to ciclosporin - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd20462046 - Nephropathy due to ciclosporin - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd21312131 - Nephropathy due to cisplatin - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd21202120 - Nephropathy due to cisplatin - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd26812681 - Nephropathy due to eclampsia
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd21542154 - Nephropathy due to lithium - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd21492149 - Nephropathy due to lithium - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd38343834 - Nephropathy due to pre-eclampsia
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd20792079 - Nephropathy due to tacrolimus - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd20672067 - Nephropathy due to tacrolimus - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd22882288 - Nephropathy related to HIV - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd22742274 - Nephropathy related to HIV - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd36153615 - Nephrotic syndrome of childhood - no trial of steroids - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd36043604 - Nephrotic syndrome of childhood - steroid resistant - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd10191019 - Nephrotic syndrome of childhood - steroid sensitive - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd17991799 - Obstructive nephropathy due to bladder cancer
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd18091809 - Obstructive nephropathy due to other malignancies
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd17811781 - Obstructive nephropathy due to prostate cancer
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd17751775 - Obstructive nephropathy due to prostatic hypertrophy
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd17341734 - Oligomeganephronia
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd23002300 - Other specific infection
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd30633063 - Phosphoribosyl pyrophosphate synthetase (PRPPS) superactivity
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd14551455 - Polyarteritis nodosa
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd16871687 - Posterior urethral valves
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd29012901 - Primary Fanconi syndrome
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd12671267 - Primary focal segmental glomerulosclerosis (FSGS)
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd31943194 - Primary hyperoxaluria
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd32073207 - Primary hyperoxaluria type I
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd32113211 - Primary hyperoxaluria type II
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd37313731 - Primary hyperoxaluria type III
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd16021602 - Primary reflux nephropathy - sporadic
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd30003000 - Primary renal tubular acidosis (RTA)
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd30163016 - Proximal renal tubular acidosis (RTA) - type II
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd31413141 - Pseudohypoaldosteronism type 1
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd31563156 - Pseudohypoaldosteronism type 2 (Gordon syndrome)
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd22192219 - Radiation nephritis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd22262226 - Renal / perinephric abscess
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd25092509 - Renal amyloidosis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd24692469 - Renal arterial thrombosis / occlusion
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd24242424 - Renal artery stenosis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd34743474 - Renal cell carcinoma - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd36583658 - Renal coloboma syndrome
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd36273627 - Renal cysts and diabetes syndrome
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd16411641 - Renal dysplasia due to fetal ACE-inhibitor exposure
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd36913691 - Renal failure
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd17471747 - Renal papillary necrosis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd37963796 - Renal papillary necrosis caused by analgesics
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd37833783 - Renal papillary necrosis caused by diabetes
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd38063806 - Renal papillary necrosis caused by sickle cell
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd19761976 - Renal sarcoidosis - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd19691969 - Renal sarcoidosis - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd15361536 - Renal scleroderma / systemic sclerosis - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd15271527 - Renal scleroderma / systemic sclerosis - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd22352235 - Renal tuberculosis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd24762476 - Renal vein thrombosis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd36893689 - Retroperitoneal fibrosis secondary to drugs
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd18211821 - Retroperitoneal fibrosis secondary to malignancies
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd36703670 - Retroperitoneal fibrosis secondary to peri-aortitis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd32693269 - Rubinstein-Taybi syndrome
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd22902290 - Schistosomiasis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd27022702 - Sickle cell nephropathy - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd26992699 - Sickle cell nephropathy - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd35173517 - Single kidney identified in adulthood
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd16941694 - Syndrome of agenesis of abdominal muscles - prune belly syndrome
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd14931493 - Systemic lupus erythematosus / nephritis - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd14861486 - Systemic lupus erythematosus / nephritis - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd13831383 - Systemic vasculitis - ANCA negative - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd38473847 - Systemic vasculitis - ANCA negative - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd38523852 - Systemic vasculitis - ANCA positive - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd13961396 - Systemic vasculitis - ANCA positive - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd27872787 - Thin basement membrane disease
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd26342634 - Thrombotic thrombocytopenic purpura (TTP)
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd33463346 - Townes-Brocks syndrome
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd34883488 - Transitional cell carcinoma - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd32763276 - Tuberous sclerosis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd29172917 - Tubular disorder as part of inherited metabolic diseases
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd18971897 - Tubulointerstitial nephritis - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd18841884 - Tubulointerstitial nephritis - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd19301930 - Tubulointerstitial nephritis associated with autoimmune disease - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd19241924 - Tubulointerstitial nephritis associated with autoimmune disease - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd19531953 - Tubulointerstitial nephritis with uveitis (TINU) - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd19481948 - Tubulointerstitial nephritis with uveitis (TINU) - no histology
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd18781878 - Uric acid urolithiasis
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd28272827 - Uromodulin-associated nephropathy (familial juvenile hyperuricaemic nephropathy)
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd32823282 - Von Hippel-Lindau disease
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd33333333 - Williams syndrome
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd34903490 - Wilms tumour - histologically proven
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd32483248 - Xanthinuria
https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes  prd22612261 - Xanthogranulomatous pyelonephritis

Explanation of the columns that may appear on this page:

Level A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies
System The source of the definition of the code (when the value set draws in codes defined elsewhere)
Code The code (used as the code in the resource instance)
Display The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application
Definition An explanation of the meaning of the concept
Comments Additional notes about how to use the code