KIP Infrastructure
2.12.0 - 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 2.12.0 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: 2.12.0
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
    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 v2.12.0 (CodeSystem)

This value set contains 284 concepts

CodeSystemDisplayDefinition
  prd2513https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2513 - AA amyloid secondary to chronic inflammationAA amyloid secondary to chronic inflammation
  prd1768https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1768 - Acquired obstructive nephropathy due to neurogenic bladderAcquired obstructive nephropathy due to neurogenic bladder
  prd1752https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1752 - Acquired obstructive uropathy / nephropathy Acquired obstructive uropathy / nephropathy
  prd3442https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3442 - Acute cortical necrosisAcute cortical necrosis
  prd3380https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3380 - Acute kidney injuryAcute kidney injury
  prd3403https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3403 - Acute kidney injury due to circulatory failureAcute kidney injury due to circulatory failure
  prd3398https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3398 - Acute kidney injury due to hypovolaemia Acute kidney injury due to hypovolaemia
  prd3435https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3435 - Acute kidney injury due to nephrotoxicityAcute kidney injury due to nephrotoxicity
  prd3426https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3426 - Acute kidney injury due to rhabdomyolysisAcute kidney injury due to rhabdomyolysis
  prd3419https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3419 - Acute kidney injury due to sepsisAcute kidney injury due to sepsis
  prd3457https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3457 - Acute pyelonephritisAcute pyelonephritis
  prd2196https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2196 - Acute urate nephropathy - histologically provenAcute urate nephropathy - histologically proven
  prd2183https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2183 - Acute urate nephropathy - no histologyAcute urate nephropathy - no histology
  prd1003https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1003 - Adult nephrotic syndrome - no histologyAdult nephrotic syndrome - no histology
  prd2392https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2392 - Ageing kidney - no histologyAgeing kidney - no histology
  prd2521https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2521 - AL amyloid secondary to plasma cell dyscrasiaAL amyloid secondary to plasma cell dyscrasia
  prd3071https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3071 - Alagille syndromeAlagille syndrome
  prd2760https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2760 - Alport syndrome - histologically provenAlport syndrome - histologically proven
  prd2756https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2756 - Alport syndrome - no histologyAlport syndrome - no histology
  prd1472https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1472 - Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - histologically provenAnti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - histologically proven
  prd1464https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1464 - Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - no histologyAnti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - no histology
  prd3118https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3118 - Apparent mineralocorticoid excessApparent mineralocorticoid excess
  prd1995https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1995 - Aristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - histologically provenAristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - histologically proven
  prd1982https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1982 - Aristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - no histologyAristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - no histology
  prd2448https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2448 - Atheroembolic renal disease - histologically provenAtheroembolic renal disease - histologically proven
  prd2430https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2430 - Atheroembolic renal disease - no histologyAtheroembolic renal disease - no histology
  prd2623https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2623 - Atypical haemolytic uraemic syndrome (HUS) - diarrhoea negativeAtypical haemolytic uraemic syndrome (HUS) - diarrhoea negative
  prd2718https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2718 - Autosomal dominant (AD) polycystic kidney diseaseAutosomal dominant (AD) polycystic kidney disease
  prd2725https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2725 - Autosomal dominant (AD) polycystic kidney disease type IAutosomal dominant (AD) polycystic kidney disease type I
  prd2739https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2739 - Autosomal dominant (AD) polycystic kidney disease type IIAutosomal dominant (AD) polycystic kidney disease type II
  prd2741https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2741 - Autosomal recessive (AR) polycystic kidney diseaseAutosomal recessive (AR) polycystic kidney disease
  prd3085https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3085 - Bartter syndromeBartter syndrome
  prd2773https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2773 - Benign familial haematuriaBenign familial haematuria
  prd1710https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1710 - Bladder exstrophyBladder exstrophy
  prd3322https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3322 - Branchio-oto-renal syndromeBranchio-oto-renal syndrome
  prd1845https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1845 - Calcium oxalate urolithiasisCalcium oxalate urolithiasis
  prd1832https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1832 - Calculus nephropathy / urolithiasisCalculus nephropathy / urolithiasis
  prd2482https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2482 - Cardiorenal syndromeCardiorenal syndrome
  prd2363https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2363 - Chronic hypertensive nephropathy - histologically provenChronic hypertensive nephropathy - histologically proven
  prd2359https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2359 - Chronic hypertensive nephropathy - no histologyChronic hypertensive nephropathy - no histology
  prd3564https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3564 - 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
  prd3555https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3555 - 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
  prd3529https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3529 - Chronic kidney disease (CKD) / chronic renal failure (CRF) caused by tumour nephrectomyChronic kidney disease (CKD) / chronic renal failure (CRF) caused by tumour nephrectomy
  prd3540https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3540 - Chronic kidney disease (CKD) / chronic renal failure (CRF) due to donor nephrectomyChronic kidney disease (CKD) / chronic renal failure (CRF) due to donor nephrectomy
  prd3538https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3538 - 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
  prd3708https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3708 - Chronic renal failureChronic renal failure
  prd3643https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3643 - Chronic renal failure due to systemic infectionChronic renal failure due to systemic infection
  prd2203https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2203 - Chronic urate nephropathy - histologically provenChronic urate nephropathy - histologically proven
  prd3636https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3636 - Chronic urate nephropathy - no histologyChronic urate nephropathy - no histology
  prd1440https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1440 - Churg-Strauss syndrome - histologically provenChurg-Strauss syndrome - histologically proven
  prd1438https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1438 - Churg-Strauss syndrome - no histologyChurg-Strauss syndrome - no histology
  prd1625https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1625 - Congenital dysplasia / hypoplasiaCongenital dysplasia / hypoplasia
  prd2652https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2652 - Congenital haemolytic uraemic syndromeCongenital haemolytic uraemic syndrome (HUS)
  prd1088https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1088 - Congenital nephrotic syndrome (CNS) - congenital infectionCongenital nephrotic syndrome (CNS) - congenital infection
  prd1057https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1057 - Congenital nephrotic syndrome (CNS) - diffuse mesangial sclerosisCongenital nephrotic syndrome (CNS) - diffuse mesangial sclerosis
  prd1042https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1042 - Congenital nephrotic syndrome (CNS) - Finnish type - histologically provenCongenital nephrotic syndrome (CNS) - Finnish type - histologically proven
  prd1035https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1035 - Congenital nephrotic syndrome (CNS) - Finnish type - no histologyCongenital nephrotic syndrome (CNS) - Finnish type - no histology
  prd1061https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1061 - Congenital nephrotic syndrome (CNS) - focal segmental glomerulosclerosisCongenital nephrotic syndrome (CNS) - focal segmental glomerulosclerosis (FSGS)
  prd1026https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1026 - Congenital nephrotic syndrome - no histologyCongenital nephrotic syndrome (CNS) - no histology
  prd1706https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1706 - Congenital neurogenic bladderCongenital neurogenic bladder
  prd1660https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1660 - Congenital pelvi-ureteric junction obstructionCongenital pelvi-ureteric junction obstruction
  prd1673https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1673 - Congenital vesico-ureteric junction obstructionCongenital vesico-ureteric junction obstruction
  prd1570https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1570 - Cryoglobulinaemia secondary to hepatitis C - histologically provenCryoglobulinaemia secondary to hepatitis C - histologically proven
  prd1562https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1562 - Cryoglobulinaemia secondary to hepatitis C - no histologyCryoglobulinaemia secondary to hepatitis C - no histology
  prd1591https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1591 - Cryoglobulinaemia secondary to systemic disease - histologically provenCryoglobulinaemia secondary to systemic disease - histologically proven
  prd1589https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1589 - Cryoglobulinaemia secondary to systemic disease - no histologyCryoglobulinaemia secondary to systemic disease - no histology
  prd2794https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2794 - Cystic kidney diseaseCystic kidney disease
  prd2964https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2964 - CystinosisCystinosis
  prd2955https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2955 - CystinuriaCystinuria
  prd2929https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2929 - Dent diseaseDent disease
  prd1074https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1074 - Denys-Drash syndromeDenys-Drash syndrome
  prd2328https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2328 - Diabetic nephropathy in type I diabetes - histologically provenDiabetic nephropathy in type I diabetes - histologically proven
  prd2316https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2316 - Diabetic nephropathy in type I diabetes - no histologyDiabetic nephropathy in type I diabetes - no histology
  prd2344https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2344 - Diabetic nephropathy in type II diabetes - histologically provenDiabetic nephropathy in type II diabetes - histologically proven
  prd2337https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2337 - Diabetic nephropathy in type II diabetes - no histologyDiabetic nephropathy in type II diabetes - no histology
  prd1331https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1331 - Diffuse endocapillary glomerulonephritisDiffuse endocapillary glomerulonephritis
  prd3028https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3028 - Distal renal tubular acidosis - type IDistal renal tubular acidosis (RTA) - type I
  prd3037https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3037 - Distal renal tubular acidosis with sensorineural deafness - gene mutationsDistal renal tubular acidosis with sensorineural deafness - gene mutations
  prd2005https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2005 - Drug-induced tubulointerstitial nephritis - no histologyDrug-induced tubulointerstitial nephritis - no histology
  prd2014https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2014 - Drug-induced tubulointerstitial nephritis - histologically provenDrug-induced tubulointerstitial nephritis - histologically proven
  prd1850https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1850 - Enteric hyperoxaluriaEnteric hyperoxaluria
  prd1558https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1558 - Essential mixed cryoglobulinaemia - histologically provenEssential mixed cryoglobulinaemia - histologically proven
  prd1543https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1543 - Essential mixed cryoglobulinaemia - no histologyEssential mixed cryoglobulinaemia - no histology
  prd3230https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3230 - Fabry disease - histologically provenFabry disease - histologically proven
  prd3224https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3224 - Fabry disease - no histologyFabry disease - no histology
  prd2545https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2545 - Familial amyloid secondary to protein mutations - histologically provenFamilial amyloid secondary to protein mutations - histologically proven
  prd2532https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2532 - Familial amyloid secondary to protein mutations - no histologyFamilial amyloid secondary to protein mutations - no histology
  prd1308https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1308 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - histologically provenFamilial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - histologically proven
  prd1298https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1298 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - no histologyFamilial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - no histology
  prd1280https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1280 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - histologically provenFamilial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - histologically proven
  prd1279https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1279 - Familial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - no histologyFamilial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - no histology
  prd2668https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2668 - Familial haemolytic uraemic syndrome (HUS)Familial haemolytic uraemic syndrome (HUS)
  prd3173https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3173 - Familial hypercalciuric hypocalcaemiaFamilial hypercalciuric hypocalcaemia
  prd3160https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3160 - Familial hypocalciuric hypercalcaemiaFamilial hypocalciuric hypercalcaemia
  prd3187https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3187 - Familial hypomagnesaemiaFamilial hypomagnesaemia
  prd1144https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1144 - Familial IgA nephropathy - histologically provenFamilial IgA nephropathy - histologically proven
  prd1137https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1137 - Familial IgA nephropathy - no histologyFamilial IgA nephropathy - no histology
  prd1911https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1911 - Familial interstitial nephropathy - histologically provenFamilial interstitial nephropathy - histologically proven
  prd1907https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1907 - Familial interstitial nephropathy - no histologyFamilial interstitial nephropathy - no histology
  prd3379https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3379 - Familial nephropathyFamilial nephropathy
  prd1618https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1618 - Familial reflux nephropathyFamilial reflux nephropathy
  prd2675https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2675 - Familial thrombotic thrombocytopenic purpura(2675)Familial thrombotic thrombocytopenic purpura (TTP)
  prd2566https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2566 - 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
  prd2550https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2550 - 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
  prd2453https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2453 - Fibromuscular dysplasia of renal arteryFibromuscular dysplasia of renal artery
  prd1354https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1354 - Focal and segmental proliferative glomerulonephritisFocal and segmental proliferative glomerulonephritis
  prd3754https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3754 - Focal segmental glomerulosclerosis (FSGS) secondary to HIV Focal segmental glomerulosclerosis (FSGS) secondary to HIV
  prd3765https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3765 - Focal segmental glomerulosclerosis (FSGS) secondary to lithium Focal segmental glomerulosclerosis (FSGS) secondary to lithium
  prd1320https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1320 - Focal segmental glomerulosclerosis (FSGS) secondary to obesity - histologically provenFocal segmental glomerulosclerosis (FSGS) secondary to obesity - histologically proven
  prd1312https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1312 - Focal segmental glomerulosclerosis (FSGS) secondary to obesity - no histologyFocal segmental glomerulosclerosis (FSGS) secondary to obesity - no histology
  prd3777https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3777 - Focal segmental glomerulosclerosis secondary to sickle cellFocal segmental glomerulosclerosis (FSGS) secondary to sickle cell
  prd3314https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3314 - Frasier syndromeFrasier syndrome
  prd3092https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3092 - Gitelman syndromeGitelman syndrome
  prd1656https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1656 - Glomerulocystic diseaseGlomerulocystic disease
  prd1377https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1377 - Glomerulonephritis - histologically indeterminateGlomerulonephritis - histologically indeterminate
  prd3749https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3749 - Glomerulonephritis - no histologyGlomerulonephritis - no histology
  prd1365https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1365 - Glomerulonephritis - secondary to systemic diseaseGlomerulonephritis - secondary to systemic disease
  prd3125https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3125 - Glucocorticoid suppressible hyperaldosteronismGlucocorticoid suppressible hyperaldosteronism
  prd1417https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1417 - Granulomatosis with polyangiitis - histologically provenGranulomatosis with polyangiitis - histologically proven
  prd1401https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1401 - Granulomatosis with polyangiitis - no histologyGranulomatosis with polyangiitis - no histology
  prd3572https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3572 - Haematuria and proteinuria - no histologyHaematuria and proteinuria - no histology
  prd2610https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2610 - Haemolytic uraemic syndrome (HUS) - diarrhoea associatedHaemolytic uraemic syndrome (HUS) - diarrhoea associated
  prd2647https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2647 - Haemolytic uraemic syndrome (HUS) secondary to systemic diseaseHaemolytic uraemic syndrome (HUS) secondary to systemic disease
  prd2257https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2257 - Hantavirus nephropathyHantavirus nephropathy
  prd1515https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1515 - Henoch-Schönlein purpura / nephritis - histologically provenHenoch-Schönlein purpura / nephritis - histologically proven
  prd1504https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1504 - Henoch-Schönlein purpura / nephritis - no histologyHenoch-Schönlein purpura / nephritis - no histology
  prd2495https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2495 - Hepatorenal syndromeHepatorenal syndrome
  prd3305https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3305 - Horse-shoe kidneyHorse-shoe kidney
  prd3662https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3662 - Hypercalcaemic nephropathyHypercalcaemic nephropathy
  prd2993https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2993 - Hypophosphataemic rickets autosomal recessive (AR)Hypophosphataemic rickets autosomal recessive (AR)
  prd2986https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2986 - Hypophosphataemic rickets X-linked (XL)Hypophosphataemic rickets X-linked (XL)
  prd1251https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1251 - Idiopathic rapidly progressive (crescentic) glomerulonephritisIdiopathic rapidly progressive (crescentic) glomerulonephritis
  prd1813https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1813 - Idiopathic retroperitoneal fibrosisIdiopathic retroperitoneal fibrosis
  prd1128https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1128 - IgA nephropathy - histologically provenIgA nephropathy - histologically proven
  prd1116https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1116 - IgA nephropathy - no histologyIgA nephropathy - no histology
  prd1163https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1163 - IgA nephropathy secondary to liver cirrhosis - histologically provenIgA nephropathy secondary to liver cirrhosis - histologically proven
  prd1159https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1159 - IgA nephropathy secondary to liver cirrhosis - no histologyIgA nephropathy secondary to liver cirrhosis - no histology
  prd1171https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1171 - IgM - associated nephropathyIgM - associated nephropathy
  prd2606https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2606 - Immunotactoid / fibrillary nephropathyImmunotactoid / fibrillary nephropathy
  prd3823https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3823 - Infiltration by lymphoma - histologically provenInfiltration by lymphoma - histologically proven
  prd3139https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3139 - Inherited / genetic diabetes mellitus type IIInherited / genetic diabetes mellitus type II
  prd2940https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2940 - Inherited aminoaciduriaInherited aminoaciduria
  prd2972https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2972 - Inherited renal glycosuriaInherited renal glycosuria
  prd2407https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2407 - Ischaemic nephropathy - no histologyIschaemic nephropathy - no histology
  prd2411https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2411 - Ischaemic nephropathy / microvascular disease - histologically provenIschaemic nephropathy / microvascular disease - histologically proven
  prd3712https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3712 - Isolated haematuria - no histologyIsolated haematuria - no histology
  prd3720https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3720 - Isolated proteinuria - no histologyIsolated proteinuria - no histology
  prd3810https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3810 - Kidney stones due to ARPT deficiencyKidney stones due to ARPT deficiency
  prd3461https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3461 - Kidney tumourKidney tumour
  prd3351https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3351 - Lawrence-Moon-Biedl / Bardet-Biedl syndromeLawrence-Moon-Biedl / Bardet-Biedl syndrome
  prd2177https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2177 - Lead induced nephropathy - histologically provenLead induced nephropathy - histologically proven
  prd2165https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2165 - Lead induced nephropathy - no histologyLead induced nephropathy - no histology
  prd2242https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2242 - LeptospirosisLeptospirosis
  prd3059https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3059 - Lesch Nyhan syndrome - hypoxanthine guanine phosphoribosyl transferase deficiencyLesch Nyhan syndrome - hypoxanthine guanine phosphoribosyl transferase deficiency
  prd3102https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3102 - Liddle syndromeLiddle syndrome
  prd2597https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2597 - Light chain deposition diseaseLight chain deposition disease
  prd2938https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2938 - Lowe syndrome (oculocerebrorenal syndrome)Lowe syndrome (oculocerebrorenal syndrome)
  prd1866https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1866 - Magnesium ammonium phosphate (struvite) urolithiasisMagnesium ammonium phosphate (struvite) urolithiasis
  prd2385https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2385 - Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - histologically provenMalignant hypertensive nephropathy / accelerated hypertensive nephropathy - histologically proven
  prd2371https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2371 - Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - no histologyMalignant hypertensive nephropathy / accelerated hypertensive nephropathy - no histology
  prd2804https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2804 - Medullary cystic kidney disease type IMedullary cystic kidney disease type I
  prd2815https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2815 - Medullary cystic kidney disease type IIMedullary cystic kidney disease type II
  prd3295https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3295 - Medullary sponge kidneysMedullary sponge kidneys
  prd1723https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1723 - Megacystis-megaureterMegacystis-megaureter
  prd1205https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1205 - Membranous nephropathy - drug inducedMembranous nephropathy - drug induced
  prd1185https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1185 - Membranous nephropathy - idiopathicMembranous nephropathy - idiopathic
  prd1214https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1214 - Membranous nephropathy - infection associatedMembranous nephropathy - infection associated
  prd1192https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1192 - Membranous nephropathy - malignancy associatedMembranous nephropathy - malignancy associated
  prd1349https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1349 - Mesangial proliferative glomerulonephritis Mesangial proliferative glomerulonephritis
  prd1222https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1222 - Mesangiocapillary glomerulonephritis type 1Mesangiocapillary glomerulonephritis type 1
  prd1233https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1233 - Mesangiocapillary glomerulonephritis type 2 (dense deposit disease)Mesangiocapillary glomerulonephritis type 2 (dense deposit disease)
  prd1246https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1246 - Mesangiocapillary glomerulonephritis type 3Mesangiocapillary glomerulonephritis type 3
  prd3501https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3501 - Mesoblastic nephroma - histologically provenMesoblastic nephroma - histologically proven
  prd1429https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1429 - Microscopic polyangiitis - histologically provenMicroscopic polyangiitis - histologically proven
  prd1100https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1100 - Minimal change nephropathy - histologically provenMinimal change nephropathy - histologically proven
  prd1090https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1090 - Minimal change nephropathy - no histologyMinimal change nephropathy - no histology
  prd3367https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3367 - Mitochondrial cytopathyMitochondrial cytopathy
  prd1639https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1639 - Multicystic dysplastic kidneysMulticystic dysplastic kidneys
  prd2584https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2584 - Myeloma cast nephropathy - histologically provenMyeloma cast nephropathy - histologically proven
  prd2578https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2578 - Myeloma kidney - no histologyMyeloma kidney - no histology
  prd3253https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3253 - Nail-patella syndromeNail-patella syndrome
  prd3044https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3044 - Nephrogenic diabetes insipidusNephrogenic diabetes insipidus
  prd2836https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2836 - NephronophthisisNephronophthisis
  prd2843https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2843 - Nephronophthisis - type 1 (juvenile type)Nephronophthisis - type 1 (juvenile type)
  prd2858https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2858 - Nephronophthisis - type 2 (infantile type)Nephronophthisis - type 2 (infantile type)
  prd2862https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2862 - Nephronophthisis - type 3 (adolescent type)Nephronophthisis - type 3 (adolescent type)
  prd2870https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2870 - Nephronophthisis - type 4 (juvenile type)Nephronophthisis - type 4 (juvenile type)
  prd2889https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2889 - Nephronophthisis - type 5Nephronophthisis - type 5
  prd2891https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2891 - Nephronophthisis - type 6Nephronophthisis - type 6
  prd2098https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2098 - Nephropathy due to aminoglycosides - histologically provenNephropathy due to aminoglycosides - histologically proven
  prd2080https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2080 - Nephropathy due to aminoglycosides - no histologyNephropathy due to aminoglycosides - no histology
  prd2112https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2112 - Nephropathy due to amphotericin - histologically provenNephropathy due to amphotericin - histologically proven
  prd2108https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2108 - Nephropathy due to amphotericin - no histologyNephropathy due to amphotericin - no histology
  prd2033https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2033 - Nephropathy due to analgesic drugs - histologically provenNephropathy due to analgesic drugs - histologically proven
  prd2022https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2022 - Nephropathy due to analgesic drugs - no histologyNephropathy due to analgesic drugs - no histology
  prd2051https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2051 - Nephropathy due to ciclosporin - histologically provenNephropathy due to ciclosporin - histologically proven
  prd2046https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2046 - Nephropathy due to ciclosporin - no histologyNephropathy due to ciclosporin - no histology
  prd2131https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2131 - Nephropathy due to cisplatin - histologically provenNephropathy due to cisplatin - histologically proven
  prd2120https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2120 - Nephropathy due to cisplatin - no histologyNephropathy due to cisplatin - no histology
  prd2681https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2681 - Nephropathy due to eclampsiaNephropathy due to eclampsia
  prd2154https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2154 - Nephropathy due to lithium - histologically provenNephropathy due to lithium - histologically proven
  prd2149https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2149 - Nephropathy due to lithium - no histologyNephropathy due to lithium - no histology
  prd3834https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3834 - Nephropathy due to pre-eclampsiaNephropathy due to pre-eclampsia
  prd2079https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2079 - Nephropathy due to tacrolimus - histologically provenNephropathy due to tacrolimus - histologically proven
  prd2067https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2067 - Nephropathy due to tacrolimus - no histologyNephropathy due to tacrolimus - no histology
  prd2288https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2288 - Nephropathy related to HIV - histologically provenNephropathy related to HIV - histologically proven
  prd2274https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2274 - Nephropathy related to HIV - no histologyNephropathy related to HIV - no histology
  prd3615https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3615 - Nephrotic syndrome of childhood - no trial of steroids - no histologyNephrotic syndrome of childhood - no trial of steroids - no histology
  prd3604https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3604 - Nephrotic syndrome of childhood - steroid resistant - no histologyNephrotic syndrome of childhood - steroid resistant - no histology
  prd1019https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1019 - Nephrotic syndrome of childhood - steroid sensitive - no histologyNephrotic syndrome of childhood - steroid sensitive - no histology
  prd1799https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1799 - Obstructive nephropathy due to bladder cancerObstructive nephropathy due to bladder cancer
  prd1809https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1809 - Obstructive nephropathy due to other malignanciesObstructive nephropathy due to other malignancies
  prd1781https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1781 - Obstructive nephropathy due to prostate cancerObstructive nephropathy due to prostate cancer
  prd1775https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1775 - Obstructive nephropathy due to prostatic hypertrophyObstructive nephropathy due to prostatic hypertrophy
  prd1734https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1734 - OligomeganephroniaOligomeganephronia
  prd2300https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2300 - Other specific infectionOther specific infection
  prd3063https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3063 - Phosphoribosyl pyrophosphate synthetase (PRPPS) superactivityPhosphoribosyl pyrophosphate synthetase (PRPPS) superactivity
  prd1455https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1455 - Polyarteritis nodosaPolyarteritis nodosa
  prd1687https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1687 - Posterior urethral valvesPosterior urethral valves
  prd2901https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2901 - Primary Fanconi syndromePrimary Fanconi syndrome
  prd1267https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1267 - Primary focal segmental glomerulosclerosis (FSGS)Primary focal segmental glomerulosclerosis (FSGS)
  prd3194https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3194 - Primary hyperoxaluriaPrimary hyperoxaluria
  prd3207https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3207 - Primary hyperoxaluria type IPrimary hyperoxaluria type I
  prd3211https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3211 - Primary hyperoxaluria type IIPrimary hyperoxaluria type II
  prd3731https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3731 - Primary hyperoxaluria type IIIPrimary hyperoxaluria type III
  prd1602https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1602 - Primary reflux nephropathy - sporadicPrimary reflux nephropathy - sporadic
  prd3000https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3000 - Primary renal tubular acidosis (RTA)Primary renal tubular acidosis (RTA)
  prd3016https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3016 - Proximal renal tubular acidosis (RTA) - type IIProximal renal tubular acidosis (RTA) - type II
  prd3141https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3141 - Pseudohypoaldosteronism type 1Pseudohypoaldosteronism type 1
  prd3156https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3156 - Pseudohypoaldosteronism type 2 (Gordon syndrome)Pseudohypoaldosteronism type 2 (Gordon syndrome)
  prd2219https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2219 - Radiation nephritisRadiation nephritis
  prd2226https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2226 - Renal / perinephric abscessRenal / perinephric abscess
  prd2509https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2509 - Renal amyloidosisRenal amyloidosis
  prd2469https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2469 - Renal arterial thrombosis / occlusionRenal arterial thrombosis / occlusion
  prd2424https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2424 - Renal artery stenosisRenal artery stenosis
  prd3474https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3474 - Renal cell carcinoma - histologically provenRenal cell carcinoma - histologically proven
  prd3658https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3658 - Renal coloboma syndromeRenal coloboma syndrome
  prd3627https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3627 - Renal cysts and diabetes syndromeRenal cysts and diabetes syndrome
  prd1641https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1641 - Renal dysplasia due to fetal ACE-inhibitor exposureRenal dysplasia due to fetal ACE-inhibitor exposure
  prd3691https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3691 - Renal failureRenal failure
  prd1747https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1747 - Renal papillary necrosisRenal papillary necrosis
  prd3796https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3796 - Renal papillary necrosis caused by analgesicsRenal papillary necrosis caused by analgesics
  prd3783https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3783 - Renal papillary necrosis caused by diabetesRenal papillary necrosis caused by diabetes
  prd3806https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3806 - Renal papillary necrosis caused by sickle cellRenal papillary necrosis caused by sickle cell
  prd1976https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1976 - Renal sarcoidosis - histologically provenRenal sarcoidosis - histologically proven
  prd1969https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1969 - Renal sarcoidosis - no histologyRenal sarcoidosis - no histology
  prd1536https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1536 - Renal scleroderma / systemic sclerosis - histologically provenRenal scleroderma / systemic sclerosis - histologically proven
  prd1527https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1527 - Renal scleroderma / systemic sclerosis - no histologyRenal scleroderma / systemic sclerosis - no histology
  prd2235https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2235 - Renal tuberculosisRenal tuberculosis
  prd2476https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2476 - Renal vein thrombosisRenal vein thrombosis
  prd3689https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3689 - Retroperitoneal fibrosis secondary to drugsRetroperitoneal fibrosis secondary to drugs
  prd1821https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1821 - Retroperitoneal fibrosis secondary to malignanciesRetroperitoneal fibrosis secondary to malignancies
  prd3670https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3670 - Retroperitoneal fibrosis secondary to peri-aortitisRetroperitoneal fibrosis secondary to peri-aortitis
  prd3269https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3269 - Rubinstein-Taybi syndromeRubinstein-Taybi syndrome
  prd2290https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2290 - SchistosomiasisSchistosomiasis
  prd2702https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2702 - Sickle cell nephropathy - histologically provenSickle cell nephropathy - histologically proven
  prd2699https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2699 - Sickle cell nephropathy - no histologySickle cell nephropathy - no histology
  prd3517https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3517 - Single kidney identified in adulthoodSingle kidney identified in adulthood
  prd1694https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1694 - Syndrome of agenesis of abdominal muscles - prune belly syndromeSyndrome of agenesis of abdominal muscles - prune belly syndrome
  prd1493https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1493 - Systemic lupus erythematosus / nephritis - histologically provenSystemic lupus erythematosus / nephritis - histologically proven
  prd1486https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1486 - Systemic lupus erythematosus / nephritis - no histologySystemic lupus erythematosus / nephritis - no histology
  prd1383https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1383 - Systemic vasculitis - ANCA negative - histologically provenSystemic vasculitis - ANCA negative - histologically proven
  prd3847https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3847 - Systemic vasculitis - ANCA negative - no histologySystemic vasculitis - ANCA negative - no histology
  prd3852https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3852 - Systemic vasculitis - ANCA positive - histologically provenSystemic vasculitis - ANCA positive - histologically proven
  prd1396https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1396 - Systemic vasculitis - ANCA positive - no histologySystemic vasculitis - ANCA positive - no histology
  prd2787https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2787 - Thin basement membrane diseaseThin basement membrane disease
  prd2634https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2634 - Thrombotic thrombocytopenic purpura (TTP)Thrombotic thrombocytopenic purpura (TTP)
  prd3346https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3346 - Townes-Brocks syndromeTownes-Brocks syndrome
  prd3488https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3488 - Transitional cell carcinoma - histologically provenTransitional cell carcinoma - histologically proven
  prd3276https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3276 - Tuberous sclerosisTuberous sclerosis
  prd2917https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2917 - Tubular disorder as part of inherited metabolic diseasesTubular disorder as part of inherited metabolic diseases
  prd1897https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1897 - Tubulointerstitial nephritis - histologically provenTubulointerstitial nephritis - histologically proven
  prd1884https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1884 - Tubulointerstitial nephritis - no histologyTubulointerstitial nephritis - no histology
  prd1930https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1930 - Tubulointerstitial nephritis associated with autoimmune disease - histologically provenTubulointerstitial nephritis associated with autoimmune disease - histologically proven
  prd1924https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1924 - Tubulointerstitial nephritis associated with autoimmune disease - no histologyTubulointerstitial nephritis associated with autoimmune disease - no histology
  prd1953https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1953 - Tubulointerstitial nephritis with uveitis (TINU) - histologically provenTubulointerstitial nephritis with uveitis (TINU) - histologically proven
  prd1948https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1948 - Tubulointerstitial nephritis with uveitis (TINU) - no histologyTubulointerstitial nephritis with uveitis (TINU) - no histology
  prd1878https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes1878 - Uric acid urolithiasisUric acid urolithiasis
  prd2827https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2827 - Uromodulin-associated nephropathy (familial juvenile hyperuricaemic nephropathy)Uromodulin-associated nephropathy (familial juvenile hyperuricaemic nephropathy)
  prd3282https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3282 - Von Hippel-Lindau diseaseVon Hippel-Lindau disease
  prd3333https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3333 - Williams syndromeWilliams syndrome
  prd3490https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3490 - Wilms tumour - histologically provenWilms tumour - histologically proven
  prd3248https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes3248 - XanthinuriaXanthinuria
  prd2261https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes2261 - Xanthogranulomatous pyelonephritisXanthogranulomatous 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