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0.2.1 - release

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ValueSet: ERA PRD Codes (Experimental)

Official URL: https://kip.rkkp.dk/fhir/ValueSet/PRDcodes Version: 0.2.1
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)

Generated Narrative: ValueSet PRDcodes

  • 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

ValueSet

Expansion performed internally based on codesystem ERA PRD Codes v0.2.1 (CodeSystem)

This value set contains 284 concepts

CodeSystemDisplay (en-US)Definition
  prd2513https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

AA amyloid secondary to chronic inflammation

  prd1768https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Acquired obstructive nephropathy due to neurogenic bladder

  prd1752https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Acquired obstructive uropathy / nephropathy

  prd3442https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Acute cortical necrosis

  prd3380https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Acute kidney injury

  prd3403https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Acute kidney injury due to circulatory failure

  prd3398https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Acute kidney injury due to hypovolaemia

  prd3435https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Acute kidney injury due to nephrotoxicity

  prd3426https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Acute kidney injury due to rhabdomyolysis

  prd3419https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Acute kidney injury due to sepsis

  prd3457https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Acute pyelonephritis

  prd2196https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Acute urate nephropathy - histologically proven

  prd2183https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Acute urate nephropathy - no histology

  prd1003https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Adult nephrotic syndrome - no histology

  prd2392https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Ageing kidney - no histology

  prd2521https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

AL amyloid secondary to plasma cell dyscrasia

  prd3071https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Alagille syndrome

  prd2760https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Alport syndrome - histologically proven

  prd2756https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Alport syndrome - no histology

  prd1472https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - histologically proven

  prd1464https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - no histology

  prd3118https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Apparent mineralocorticoid excess

  prd1995https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Aristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - histologically proven

  prd1982https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Aristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - no histology

  prd2448https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Atheroembolic renal disease - histologically proven

  prd2430https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Atheroembolic renal disease - no histology

  prd2623https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Atypical haemolytic uraemic syndrome (HUS) - diarrhoea negative

  prd2718https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Autosomal dominant (AD) polycystic kidney disease

  prd2725https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Autosomal dominant (AD) polycystic kidney disease type I

  prd2739https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Autosomal dominant (AD) polycystic kidney disease type II

  prd2741https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Autosomal recessive (AR) polycystic kidney disease

  prd3085https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Bartter syndrome

  prd2773https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Benign familial haematuria

  prd1710https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Bladder exstrophy

  prd3322https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Branchio-oto-renal syndrome

  prd1845https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Calcium oxalate urolithiasis

  prd1832https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Calculus nephropathy / urolithiasis

  prd2482https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Cardiorenal syndrome

  prd2363https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Chronic hypertensive nephropathy - histologically proven

  prd2359https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Chronic hypertensive nephropathy - no histology

  prd3564https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Chronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - histologically proven

  prd3555https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Chronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - no histology

  prd3529https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Chronic kidney disease (CKD) / chronic renal failure (CRF) caused by tumour nephrectomy

  prd3540https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Chronic kidney disease (CKD) / chronic renal failure (CRF) due to donor nephrectomy

  prd3538https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Chronic kidney disease (CKD) / chronic renal failure (CRF) due to traumatic loss of kidney

  prd3708https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Chronic renal failure

  prd3643https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Chronic renal failure due to systemic infection

  prd2203https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Chronic urate nephropathy - histologically proven

  prd3636https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Chronic urate nephropathy - no histology

  prd1440https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Churg-Strauss syndrome - histologically proven

  prd1438https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Churg-Strauss syndrome - no histology

  prd1625https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Congenital dysplasia / hypoplasia

  prd2652https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Congenital haemolytic uraemic syndrome (HUS)

  prd1088https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Congenital nephrotic syndrome (CNS) - congenital infection

  prd1057https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Congenital nephrotic syndrome (CNS) - diffuse mesangial sclerosis

  prd1042https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Congenital nephrotic syndrome (CNS) - Finnish type - histologically proven

  prd1035https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Congenital nephrotic syndrome (CNS) - Finnish type - no histology

  prd1061https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Congenital nephrotic syndrome (CNS) - focal segmental glomerulosclerosis (FSGS)

  prd1026https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Congenital nephrotic syndrome (CNS) - no histology

  prd1706https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Congenital neurogenic bladder

  prd1660https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Congenital pelvi-ureteric junction obstruction

  prd1673https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Congenital vesico-ureteric junction obstruction

  prd1570https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Cryoglobulinaemia secondary to hepatitis C - histologically proven

  prd1562https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Cryoglobulinaemia secondary to hepatitis C - no histology

  prd1591https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Cryoglobulinaemia secondary to systemic disease - histologically proven

  prd1589https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Cryoglobulinaemia secondary to systemic disease - no histology

  prd2794https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Cystic kidney disease

  prd2964https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Cystinosis

  prd2955https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Cystinuria

  prd2929https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Dent disease

  prd1074https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Denys-Drash syndrome

  prd2328https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Diabetic nephropathy in type I diabetes - histologically proven

  prd2316https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Diabetic nephropathy in type I diabetes - no histology

  prd2344https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Diabetic nephropathy in type II diabetes - histologically proven

  prd2337https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Diabetic nephropathy in type II diabetes - no histology

  prd1331https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Diffuse endocapillary glomerulonephritis

  prd3028https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Distal renal tubular acidosis (RTA) - type I

  prd3037https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Distal renal tubular acidosis with sensorineural deafness - gene mutations

  prd2005https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Drug-induced tubulointerstitial nephritis - no histology

  prd2014https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Drug-induced tubulointerstitial nephritis - histologically proven

  prd1850https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Enteric hyperoxaluria

  prd1558https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Essential mixed cryoglobulinaemia - histologically proven

  prd1543https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Essential mixed cryoglobulinaemia - no histology

  prd3230https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Fabry disease - histologically proven

  prd3224https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Fabry disease - no histology

  prd2545https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Familial amyloid secondary to protein mutations - histologically proven

  prd2532https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Familial amyloid secondary to protein mutations - no histology

  prd1308https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Familial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - histologically proven

  prd1298https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Familial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - no histology

  prd1280https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Familial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - histologically proven

  prd1279https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Familial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - no histology

  prd2668https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Familial haemolytic uraemic syndrome (HUS)

  prd3173https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Familial hypercalciuric hypocalcaemia

  prd3160https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Familial hypocalciuric hypercalcaemia

  prd3187https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Familial hypomagnesaemia

  prd1144https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Familial IgA nephropathy - histologically proven

  prd1137https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Familial IgA nephropathy - no histology

  prd1911https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Familial interstitial nephropathy - histologically proven

  prd1907https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Familial interstitial nephropathy - no histology

  prd3379https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Familial nephropathy

  prd1618https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Familial reflux nephropathy

  prd2675https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Familial thrombotic thrombocytopenic purpura (TTP)

  prd2566https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Familial AA amyloid secondary to familial Mediterranean fever / TRAPS (Hibernian fever) - histologically proven

  prd2550https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Familial AA amyloid secondary to familial Mediterranean fever / TRAPS (Hibernian fever) - no histology

  prd2453https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Fibromuscular dysplasia of renal artery

  prd1354https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Focal and segmental proliferative glomerulonephritis

  prd3754https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Focal segmental glomerulosclerosis (FSGS) secondary to HIV

  prd3765https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Focal segmental glomerulosclerosis (FSGS) secondary to lithium

  prd1320https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Focal segmental glomerulosclerosis (FSGS) secondary to obesity - histologically proven

  prd1312https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Focal segmental glomerulosclerosis (FSGS) secondary to obesity - no histology

  prd3777https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Focal segmental glomerulosclerosis (FSGS) secondary to sickle cell

  prd3314https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Frasier syndrome

  prd3092https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Gitelman syndrome

  prd1656https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Glomerulocystic disease

  prd1377https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Glomerulonephritis - histologically indeterminate

  prd3749https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Glomerulonephritis - no histology

  prd1365https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Glomerulonephritis - secondary to systemic disease

  prd3125https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Glucocorticoid suppressible hyperaldosteronism

  prd1417https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Granulomatosis with polyangiitis - histologically proven

  prd1401https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Granulomatosis with polyangiitis - no histology

  prd3572https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Haematuria and proteinuria - no histology

  prd2610https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Haemolytic uraemic syndrome (HUS) - diarrhoea associated

  prd2647https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Haemolytic uraemic syndrome (HUS) secondary to systemic disease

  prd2257https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Hantavirus nephropathy

  prd1515https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Henoch-Schönlein purpura / nephritis - histologically proven

  prd1504https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Henoch-Schönlein purpura / nephritis - no histology

  prd2495https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Hepatorenal syndrome

  prd3305https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Horse-shoe kidney

  prd3662https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Hypercalcaemic nephropathy

  prd2993https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Hypophosphataemic rickets autosomal recessive (AR)

  prd2986https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Hypophosphataemic rickets X-linked (XL)

  prd1251https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Idiopathic rapidly progressive (crescentic) glomerulonephritis

  prd1813https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Idiopathic retroperitoneal fibrosis

  prd1128https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

IgA nephropathy - histologically proven

  prd1116https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

IgA nephropathy - no histology

  prd1163https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

IgA nephropathy secondary to liver cirrhosis - histologically proven

  prd1159https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

IgA nephropathy secondary to liver cirrhosis - no histology

  prd1171https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

IgM - associated nephropathy

  prd2606https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Immunotactoid / fibrillary nephropathy

  prd3823https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Infiltration by lymphoma - histologically proven

  prd3139https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Inherited / genetic diabetes mellitus type II

  prd2940https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Inherited aminoaciduria

  prd2972https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Inherited renal glycosuria

  prd2407https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Ischaemic nephropathy - no histology

  prd2411https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Ischaemic nephropathy / microvascular disease - histologically proven

  prd3712https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Isolated haematuria - no histology

  prd3720https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Isolated proteinuria - no histology

  prd3810https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Kidney stones due to ARPT deficiency

  prd3461https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Kidney tumour

  prd3351https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Lawrence-Moon-Biedl / Bardet-Biedl syndrome

  prd2177https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Lead induced nephropathy - histologically proven

  prd2165https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Lead induced nephropathy - no histology

  prd2242https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Leptospirosis

  prd3059https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Lesch Nyhan syndrome - hypoxanthine guanine phosphoribosyl transferase deficiency

  prd3102https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Liddle syndrome

  prd2597https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Light chain deposition disease

  prd2938https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Lowe syndrome (oculocerebrorenal syndrome)

  prd1866https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Magnesium ammonium phosphate (struvite) urolithiasis

  prd2385https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - histologically proven

  prd2371https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - no histology

  prd2804https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Medullary cystic kidney disease type I

  prd2815https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Medullary cystic kidney disease type II

  prd3295https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Medullary sponge kidneys

  prd1723https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Megacystis-megaureter

  prd1205https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Membranous nephropathy - drug induced

  prd1185https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Membranous nephropathy - idiopathic

  prd1214https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Membranous nephropathy - infection associated

  prd1192https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Membranous nephropathy - malignancy associated

  prd1349https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Mesangial proliferative glomerulonephritis

  prd1222https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Mesangiocapillary glomerulonephritis type 1

  prd1233https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Mesangiocapillary glomerulonephritis type 2 (dense deposit disease)

  prd1246https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Mesangiocapillary glomerulonephritis type 3

  prd3501https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Mesoblastic nephroma - histologically proven

  prd1429https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Microscopic polyangiitis - histologically proven

  prd1100https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Minimal change nephropathy - histologically proven

  prd1090https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Minimal change nephropathy - no histology

  prd3367https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Mitochondrial cytopathy

  prd1639https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Multicystic dysplastic kidneys

  prd2584https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Myeloma cast nephropathy - histologically proven

  prd2578https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Myeloma kidney - no histology

  prd3253https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nail-patella syndrome

  prd3044https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephrogenic diabetes insipidus

  prd2836https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephronophthisis

  prd2843https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephronophthisis - type 1 (juvenile type)

  prd2858https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephronophthisis - type 2 (infantile type)

  prd2862https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephronophthisis - type 3 (adolescent type)

  prd2870https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephronophthisis - type 4 (juvenile type)

  prd2889https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephronophthisis - type 5

  prd2891https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephronophthisis - type 6

  prd2098https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephropathy due to aminoglycosides - histologically proven

  prd2080https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephropathy due to aminoglycosides - no histology

  prd2112https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephropathy due to amphotericin - histologically proven

  prd2108https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephropathy due to amphotericin - no histology

  prd2033https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephropathy due to analgesic drugs - histologically proven

  prd2022https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephropathy due to analgesic drugs - no histology

  prd2051https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephropathy due to ciclosporin - histologically proven

  prd2046https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephropathy due to ciclosporin - no histology

  prd2131https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephropathy due to cisplatin - histologically proven

  prd2120https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephropathy due to cisplatin - no histology

  prd2681https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephropathy due to eclampsia

  prd2154https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephropathy due to lithium - histologically proven

  prd2149https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephropathy due to lithium - no histology

  prd3834https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephropathy due to pre-eclampsia

  prd2079https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephropathy due to tacrolimus - histologically proven

  prd2067https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephropathy due to tacrolimus - no histology

  prd2288https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephropathy related to HIV - histologically proven

  prd2274https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephropathy related to HIV - no histology

  prd3615https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephrotic syndrome of childhood - no trial of steroids - no histology

  prd3604https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephrotic syndrome of childhood - steroid resistant - no histology

  prd1019https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Nephrotic syndrome of childhood - steroid sensitive - no histology

  prd1799https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Obstructive nephropathy due to bladder cancer

  prd1809https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Obstructive nephropathy due to other malignancies

  prd1781https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Obstructive nephropathy due to prostate cancer

  prd1775https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Obstructive nephropathy due to prostatic hypertrophy

  prd1734https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Oligomeganephronia

  prd2300https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Other specific infection

  prd3063https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Phosphoribosyl pyrophosphate synthetase (PRPPS) superactivity

  prd1455https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Polyarteritis nodosa

  prd1687https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Posterior urethral valves

  prd2901https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Primary Fanconi syndrome

  prd1267https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Primary focal segmental glomerulosclerosis (FSGS)

  prd3194https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Primary hyperoxaluria

  prd3207https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Primary hyperoxaluria type I

  prd3211https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Primary hyperoxaluria type II

  prd3731https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Primary hyperoxaluria type III

  prd1602https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Primary reflux nephropathy - sporadic

  prd3000https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Primary renal tubular acidosis (RTA)

  prd3016https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Proximal renal tubular acidosis (RTA) - type II

  prd3141https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Pseudohypoaldosteronism type 1

  prd3156https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Pseudohypoaldosteronism type 2 (Gordon syndrome)

  prd2219https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Radiation nephritis

  prd2226https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Renal / perinephric abscess

  prd2509https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Renal amyloidosis

  prd2469https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Renal arterial thrombosis / occlusion

  prd2424https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Renal artery stenosis

  prd3474https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Renal cell carcinoma - histologically proven

  prd3658https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Renal coloboma syndrome

  prd3627https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Renal cysts and diabetes syndrome

  prd1641https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Renal dysplasia due to fetal ACE-inhibitor exposure

  prd3691https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Renal failure

  prd1747https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Renal papillary necrosis

  prd3796https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Renal papillary necrosis caused by analgesics

  prd3783https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Renal papillary necrosis caused by diabetes

  prd3806https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Renal papillary necrosis caused by sickle cell

  prd1976https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Renal sarcoidosis - histologically proven

  prd1969https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Renal sarcoidosis - no histology

  prd1536https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Renal scleroderma / systemic sclerosis - histologically proven

  prd1527https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Renal scleroderma / systemic sclerosis - no histology

  prd2235https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Renal tuberculosis

  prd2476https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Renal vein thrombosis

  prd3689https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Retroperitoneal fibrosis secondary to drugs

  prd1821https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Retroperitoneal fibrosis secondary to malignancies

  prd3670https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Retroperitoneal fibrosis secondary to peri-aortitis

  prd3269https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Rubinstein-Taybi syndrome

  prd2290https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Schistosomiasis

  prd2702https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Sickle cell nephropathy - histologically proven

  prd2699https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Sickle cell nephropathy - no histology

  prd3517https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Single kidney identified in adulthood

  prd1694https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Syndrome of agenesis of abdominal muscles - prune belly syndrome

  prd1493https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Systemic lupus erythematosus / nephritis - histologically proven

  prd1486https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Systemic lupus erythematosus / nephritis - no histology

  prd1383https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Systemic vasculitis - ANCA negative - histologically proven

  prd3847https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Systemic vasculitis - ANCA negative - no histology

  prd3852https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Systemic vasculitis - ANCA positive - histologically proven

  prd1396https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Systemic vasculitis - ANCA positive - no histology

  prd2787https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Thin basement membrane disease

  prd2634https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Thrombotic thrombocytopenic purpura (TTP)

  prd3346https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Townes-Brocks syndrome

  prd3488https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Transitional cell carcinoma - histologically proven

  prd3276https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Tuberous sclerosis

  prd2917https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Tubular disorder as part of inherited metabolic diseases

  prd1897https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Tubulointerstitial nephritis - histologically proven

  prd1884https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Tubulointerstitial nephritis - no histology

  prd1930https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Tubulointerstitial nephritis associated with autoimmune disease - histologically proven

  prd1924https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Tubulointerstitial nephritis associated with autoimmune disease - no histology

  prd1953https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Tubulointerstitial nephritis with uveitis (TINU) - histologically proven

  prd1948https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Tubulointerstitial nephritis with uveitis (TINU) - no histology

  prd1878https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Uric acid urolithiasis

  prd2827https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Uromodulin-associated nephropathy (familial juvenile hyperuricaemic nephropathy)

  prd3282https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Von Hippel-Lindau disease

  prd3333https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Williams syndrome

  prd3490https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Wilms tumour - histologically proven

  prd3248https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

Xanthinuria

  prd2261https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes

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