KIP Infrastructure
2.12.2 - 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 2.12.2 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

CodeSystem: ERA PRD Codes

Official URL: https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes Version: 2.12.2
Active as of 2024-01-10 Computable Name: PRDcodes

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

This Code system is referenced in the content logical definition of the following value sets:

This case-insensitive code system https://kip.rkkp.dk/fhir/CodeSystem/PRDcodes defines the following codes:

CodeDisplayDefinition
prd1003 Adult nephrotic syndrome - no histology (1003) Adult nephrotic syndrome - no histology
prd1019 Nephrotic syndrome of childhood - steroid sensitive - no histology (1019) Nephrotic syndrome of childhood - steroid sensitive - no histology
prd1026 Congenital nephrotic syndrome (CNS) - no histology (1026) Congenital nephrotic syndrome (CNS) - no histology
prd1035 Congenital nephrotic syndrome (CNS) - Finnish type - no histology (1035) Congenital nephrotic syndrome (CNS) - Finnish type - no histology
prd1042 Congenital nephrotic syndrome (CNS) - Finnish type - histologically proven (1042) Congenital nephrotic syndrome (CNS) - Finnish type - histologically proven
prd1057 Congenital nephrotic syndrome (CNS) - diffuse mesangial sclerosis (1057) Congenital nephrotic syndrome (CNS) - diffuse mesangial sclerosis
prd1061 Congenital nephrotic syndrome (CNS) - focal segmental glomerulosclerosis (FSGS) (1061) Congenital nephrotic syndrome (CNS) - focal segmental glomerulosclerosis (FSGS)
prd1074 Denys-Drash syndrome (1074) Denys-Drash syndrome
prd1088 Congenital nephrotic syndrome (CNS) - congenital infection (1088) Congenital nephrotic syndrome (CNS) - congenital infection
prd1090 Minimal change nephropathy - no histology (1090) Minimal change nephropathy - no histology
prd1100 Minimal change nephropathy - histologically proven (1100) Minimal change nephropathy - histologically proven
prd1116 IgA nephropathy - no histology (1116) IgA nephropathy - no histology
prd1128 IgA nephropathy - histologically proven (1128) IgA nephropathy - histologically proven
prd1137 Familial IgA nephropathy - no histology (1137) Familial IgA nephropathy - no histology
prd1144 Familial IgA nephropathy - histologically proven (1144) Familial IgA nephropathy - histologically proven
prd1159 IgA nephropathy secondary to liver cirrhosis - no histology (1159) IgA nephropathy secondary to liver cirrhosis - no histology
prd1163 IgA nephropathy secondary to liver cirrhosis - histologically proven (1163) IgA nephropathy secondary to liver cirrhosis - histologically proven
prd1171 IgM - associated nephropathy (1171) IgM - associated nephropathy
prd1185 Membranous nephropathy - idiopathic (1185) Membranous nephropathy - idiopathic
prd1192 Membranous nephropathy - malignancy associated (1192) Membranous nephropathy - malignancy associated
prd1205 Membranous nephropathy - drug induced (1205) Membranous nephropathy - drug induced
prd1214 Membranous nephropathy - infection associated (1214) Membranous nephropathy - infection associated
prd1222 Mesangiocapillary glomerulonephritis type 1 (1222) Mesangiocapillary glomerulonephritis type 1
prd1233 Mesangiocapillary glomerulonephritis type 2 (dense deposit disease) (1233) Mesangiocapillary glomerulonephritis type 2 (dense deposit disease)
prd1246 Mesangiocapillary glomerulonephritis type 3 (1246) Mesangiocapillary glomerulonephritis type 3
prd1251 Idiopathic rapidly progressive (crescentic) glomerulonephritis (1251) Idiopathic rapidly progressive (crescentic) glomerulonephritis
prd1267 Primary focal segmental glomerulosclerosis (FSGS) (1267) Primary focal segmental glomerulosclerosis (FSGS)
prd1279 Familial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - no histology (1279) Familial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - no histology
prd1280 Familial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - histologically proven (1280) Familial focal segmental glomerulosclerosis (FSGS) - autosomal recessive - histologically proven
prd1298 Familial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - no histology (1298) Familial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - no histology
prd1308 Familial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - histologically proven (1308) Familial focal segmental glomerulosclerosis (FSGS) - autosomal dominant - histologically proven
prd1312 Focal segmental glomerulosclerosis (FSGS) secondary to obesity - no histology (1312) Focal segmental glomerulosclerosis (FSGS) secondary to obesity - no histology
prd1320 Focal segmental glomerulosclerosis (FSGS) secondary to obesity - histologically proven (1320) Focal segmental glomerulosclerosis (FSGS) secondary to obesity - histologically proven
prd1331 Diffuse endocapillary glomerulonephritis (1331) Diffuse endocapillary glomerulonephritis
prd1349 Mesangial proliferative glomerulonephritis (1349) Mesangial proliferative glomerulonephritis
prd1354 Focal and segmental proliferative glomerulonephritis (1354) Focal and segmental proliferative glomerulonephritis
prd1365 Glomerulonephritis - secondary to systemic disease (1365) Glomerulonephritis - secondary to systemic disease
prd1377 Glomerulonephritis - histologically indeterminate (1377) Glomerulonephritis - histologically indeterminate
prd1383 Systemic vasculitis - ANCA negative - histologically proven (1383) Systemic vasculitis - ANCA negative - histologically proven
prd1396 Systemic vasculitis - ANCA positive - no histology (1396) Systemic vasculitis - ANCA positive - no histology
prd1401 Granulomatosis with polyangiitis - no histology (1401) Granulomatosis with polyangiitis - no histology
prd1417 Granulomatosis with polyangiitis - histologically proven (1417) Granulomatosis with polyangiitis - histologically proven
prd1429 Microscopic polyangiitis - histologically proven (1429) Microscopic polyangiitis - histologically proven
prd1438 Churg-Strauss syndrome - no histology (1438) Churg-Strauss syndrome - no histology
prd1440 Churg-Strauss syndrome - histologically proven (1440) Churg-Strauss syndrome - histologically proven
prd1455 Polyarteritis nodosa (1455) Polyarteritis nodosa
prd1464 Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - no histology (1464) Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - no histology
prd1472 Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - histologically proven (1472) Anti-Glomerular basement membrane (GBM) disease / Goodpasture's syndrome - histologically proven
prd1486 Systemic lupus erythematosus / nephritis - no histology (1486) Systemic lupus erythematosus / nephritis - no histology
prd1493 Systemic lupus erythematosus / nephritis - histologically proven (1493) Systemic lupus erythematosus / nephritis - histologically proven
prd1504 Henoch-Schönlein purpura / nephritis - no histology (1504) Henoch-Schönlein purpura / nephritis - no histology
prd1515 Henoch-Schönlein purpura / nephritis - histologically proven (1515) Henoch-Schönlein purpura / nephritis - histologically proven
prd1527 Renal scleroderma / systemic sclerosis - no histology (1527) Renal scleroderma / systemic sclerosis - no histology
prd1536 Renal scleroderma / systemic sclerosis - histologically proven (1536) Renal scleroderma / systemic sclerosis - histologically proven
prd1543 Essential mixed cryoglobulinaemia - no histology (1543) Essential mixed cryoglobulinaemia - no histology
prd1558 Essential mixed cryoglobulinaemia - histologically proven (1558) Essential mixed cryoglobulinaemia - histologically proven
prd1562 Cryoglobulinaemia secondary to hepatitis C - no histology (1562) Cryoglobulinaemia secondary to hepatitis C - no histology
prd1570 Cryoglobulinaemia secondary to hepatitis C - histologically proven (1570) Cryoglobulinaemia secondary to hepatitis C - histologically proven
prd1589 Cryoglobulinaemia secondary to systemic disease - no histology (1589) Cryoglobulinaemia secondary to systemic disease - no histology
prd1591 Cryoglobulinaemia secondary to systemic disease - histologically proven (1591) Cryoglobulinaemia secondary to systemic disease - histologically proven
prd1602 Primary reflux nephropathy - sporadic (1602) Primary reflux nephropathy - sporadic
prd1618 Familial reflux nephropathy (1618) Familial reflux nephropathy
prd1625 Congenital dysplasia / hypoplasia (1625) Congenital dysplasia / hypoplasia
prd1639 Multicystic dysplastic kidneys (1639) Multicystic dysplastic kidneys
prd1641 Renal dysplasia due to fetal ACE-inhibitor exposure (1641) Renal dysplasia due to fetal ACE-inhibitor exposure
prd1656 Glomerulocystic disease (1656) Glomerulocystic disease
prd1660 Congenital pelvi-ureteric junction obstruction (1660) Congenital pelvi-ureteric junction obstruction
prd1673 Congenital vesico-ureteric junction obstruction (1673) Congenital vesico-ureteric junction obstruction
prd1687 Posterior urethral valves (1687) Posterior urethral valves
prd1694 Syndrome of agenesis of abdominal muscles - prune belly syndrome (1694) Syndrome of agenesis of abdominal muscles - prune belly syndrome
prd1706 Congenital neurogenic bladder (1706) Congenital neurogenic bladder
prd1710 Bladder exstrophy (1710) Bladder exstrophy
prd1723 Megacystis-megaureter (1723) Megacystis-megaureter
prd1734 Oligomeganephronia (1734) Oligomeganephronia
prd1747 Renal papillary necrosis (1747) Renal papillary necrosis
prd1752 Acquired obstructive uropathy / nephropathy (1752) Acquired obstructive uropathy / nephropathy
prd1768 Acquired obstructive nephropathy due to neurogenic bladder (1768) Acquired obstructive nephropathy due to neurogenic bladder
prd1775 Obstructive nephropathy due to prostatic hypertrophy (1775) Obstructive nephropathy due to prostatic hypertrophy
prd1781 Obstructive nephropathy due to prostate cancer (1781) Obstructive nephropathy due to prostate cancer
prd1799 Obstructive nephropathy due to bladder cancer (1799) Obstructive nephropathy due to bladder cancer
prd1809 Obstructive nephropathy due to other malignancies (1809) Obstructive nephropathy due to other malignancies
prd1813 Idiopathic retroperitoneal fibrosis (1813) Idiopathic retroperitoneal fibrosis
prd1821 Retroperitoneal fibrosis secondary to malignancies (1821) Retroperitoneal fibrosis secondary to malignancies
prd1832 Calculus nephropathy / urolithiasis (1832) Calculus nephropathy / urolithiasis
prd1845 Calcium oxalate urolithiasis (1845) Calcium oxalate urolithiasis
prd1850 Enteric hyperoxaluria (1850) Enteric hyperoxaluria
prd1866 Magnesium ammonium phosphate (struvite) urolithiasis (1866) Magnesium ammonium phosphate (struvite) urolithiasis
prd1878 Uric acid urolithiasis (1878) Uric acid urolithiasis
prd1884 Tubulointerstitial nephritis - no histology (1884) Tubulointerstitial nephritis - no histology
prd1897 Tubulointerstitial nephritis - histologically proven (1897) Tubulointerstitial nephritis - histologically proven
prd1907 Familial interstitial nephropathy - no histology (1907) Familial interstitial nephropathy - no histology
prd1911 Familial interstitial nephropathy - histologically proven (1911) Familial interstitial nephropathy - histologically proven
prd1924 Tubulointerstitial nephritis associated with autoimmune disease - no histology (1924) Tubulointerstitial nephritis associated with autoimmune disease - no histology
prd1930 Tubulointerstitial nephritis associated with autoimmune disease - histologically proven (1930) Tubulointerstitial nephritis associated with autoimmune disease - histologically proven
prd1948 Tubulointerstitial nephritis with uveitis (TINU) - no histology (1948) Tubulointerstitial nephritis with uveitis (TINU) - no histology
prd1953 Tubulointerstitial nephritis with uveitis (TINU) - histologically proven (1953) Tubulointerstitial nephritis with uveitis (TINU) - histologically proven
prd1969 Renal sarcoidosis - no histology (1969) Renal sarcoidosis - no histology
prd1976 Renal sarcoidosis - histologically proven (1976) Renal sarcoidosis - histologically proven
prd1982 Aristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - no histology (1982) Aristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - no histology
prd1995 Aristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - histologically proven (1995) Aristolochic acid nephropathy (Balkan / Chinese herb / endemic nephropathy) - histologically proven
prd2005 Drug-induced tubulointerstitial nephritis - no histology (2005) Drug-induced tubulointerstitial nephritis - no histology
prd2014 Drug-induced tubulointerstitial nephritis - histologically proven (2014) Drug-induced tubulointerstitial nephritis - histologically proven
prd2022 Nephropathy due to analgesic drugs - no histology (2022) Nephropathy due to analgesic drugs - no histology
prd2033 Nephropathy due to analgesic drugs - histologically proven (2033) Nephropathy due to analgesic drugs - histologically proven
prd2046 Nephropathy due to ciclosporin - no histology (2046) Nephropathy due to ciclosporin - no histology
prd2051 Nephropathy due to ciclosporin - histologically proven (2051) Nephropathy due to ciclosporin - histologically proven
prd2067 Nephropathy due to tacrolimus - no histology (2067) Nephropathy due to tacrolimus - no histology
prd2079 Nephropathy due to tacrolimus - histologically proven (2079) Nephropathy due to tacrolimus - histologically proven
prd2080 Nephropathy due to aminoglycosides - no histology (2080) Nephropathy due to aminoglycosides - no histology
prd2098 Nephropathy due to aminoglycosides - histologically proven (2098) Nephropathy due to aminoglycosides - histologically proven
prd2108 Nephropathy due to amphotericin - no histology (2108) Nephropathy due to amphotericin - no histology
prd2112 Nephropathy due to amphotericin - histologically proven (2112) Nephropathy due to amphotericin - histologically proven
prd2120 Nephropathy due to cisplatin - no histology (2120) Nephropathy due to cisplatin - no histology
prd2131 Nephropathy due to cisplatin - histologically proven (2131) Nephropathy due to cisplatin - histologically proven
prd2149 Nephropathy due to lithium - no histology (2149) Nephropathy due to lithium - no histology
prd2154 Nephropathy due to lithium - histologically proven (2154) Nephropathy due to lithium - histologically proven
prd2165 Lead induced nephropathy - no histology (2165) Lead induced nephropathy - no histology
prd2177 Lead induced nephropathy - histologically proven (2177) Lead induced nephropathy - histologically proven
prd2183 Acute urate nephropathy - no histology (2183) Acute urate nephropathy - no histology
prd2196 Acute urate nephropathy - histologically proven (2196) Acute urate nephropathy - histologically proven
prd2203 Chronic urate nephropathy - histologically proven (2203) Chronic urate nephropathy - histologically proven
prd2219 Radiation nephritis (2219) Radiation nephritis
prd2226 Renal / perinephric abscess (2226) Renal / perinephric abscess
prd2235 Renal tuberculosis (2235) Renal tuberculosis
prd2242 Leptospirosis (2242) Leptospirosis
prd2257 Hantavirus nephropathy (2257) Hantavirus nephropathy
prd2261 Xanthogranulomatous pyelonephritis (2261) Xanthogranulomatous pyelonephritis
prd2274 Nephropathy related to HIV - no histology (2274) Nephropathy related to HIV - no histology
prd2288 Nephropathy related to HIV - histologically proven (2288) Nephropathy related to HIV - histologically proven
prd2290 Schistosomiasis (2290) Schistosomiasis
prd2300 Other specific infection (2300) Other specific infection
prd2316 Diabetic nephropathy in type I diabetes - no histology (2316) Diabetic nephropathy in type I diabetes - no histology
prd2328 Diabetic nephropathy in type I diabetes - histologically proven (2328) Diabetic nephropathy in type I diabetes - histologically proven
prd2337 Diabetic nephropathy in type II diabetes - no histology (2337) Diabetic nephropathy in type II diabetes - no histology
prd2344 Diabetic nephropathy in type II diabetes - histologically proven (2344) Diabetic nephropathy in type II diabetes - histologically proven
prd2359 Chronic hypertensive nephropathy - no histology (2359) Chronic hypertensive nephropathy - no histology
prd2363 Chronic hypertensive nephropathy - histologically proven (2363) Chronic hypertensive nephropathy - histologically proven
prd2371 Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - no histology (2371) Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - no histology
prd2385 Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - histologically proven (2385) Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - histologically proven
prd2392 Ageing kidney - no histology (2392) Ageing kidney - no histology
prd2407 Ischaemic nephropathy - no histology (2407) Ischaemic nephropathy - no histology
prd2411 Ischaemic nephropathy / microvascular disease - histologically proven (2411) Ischaemic nephropathy / microvascular disease - histologically proven
prd2424 Renal artery stenosis (2424) Renal artery stenosis
prd2430 Atheroembolic renal disease - no histology (2430) Atheroembolic renal disease - no histology
prd2448 Atheroembolic renal disease - histologically proven (2448) Atheroembolic renal disease - histologically proven
prd2453 Fibromuscular dysplasia of renal artery (2453) Fibromuscular dysplasia of renal artery
prd2469 Renal arterial thrombosis / occlusion (2469) Renal arterial thrombosis / occlusion
prd2476 Renal vein thrombosis (2476) Renal vein thrombosis
prd2482 Cardiorenal syndrome (2482) Cardiorenal syndrome
prd2495 Hepatorenal syndrome (2495) Hepatorenal syndrome
prd2509 Renal amyloidosis (2509) Renal amyloidosis
prd2513 AA amyloid secondary to chronic inflammation (2513) AA amyloid secondary to chronic inflammation
prd2521 AL amyloid secondary to plasma cell dyscrasia (2521) AL amyloid secondary to plasma cell dyscrasia
prd2532 Familial amyloid secondary to protein mutations - no histology (2532) Familial amyloid secondary to protein mutations - no histology
prd2545 Familial amyloid secondary to protein mutations - histologically proven (2545) Familial amyloid secondary to protein mutations - histologically proven
prd2550 Familial AA amyloid secondary to familial Mediterranean fever / TRAPS (Hibernian fever) - no histology (2550) Familial AA amyloid secondary to familial Mediterranean fever / TRAPS (Hibernian fever) - no histology
prd2566 Familial AA amyloid secondary to familial Mediterranean fever / TRAPS (Hibernian fever) - histologically proven (2566) Familial AA amyloid secondary to familial Mediterranean fever / TRAPS (Hibernian fever) - histologically proven
prd2578 Myeloma kidney - no histology (2578) Myeloma kidney - no histology
prd2584 Myeloma cast nephropathy - histologically proven (2584) Myeloma cast nephropathy - histologically proven
prd2597 Light chain deposition disease (2597) Light chain deposition disease
prd2606 Immunotactoid / fibrillary nephropathy (2606) Immunotactoid / fibrillary nephropathy
prd2610 Haemolytic uraemic syndrome (HUS) - diarrhoea associated (2610) Haemolytic uraemic syndrome (HUS) - diarrhoea associated
prd2623 Atypical haemolytic uraemic syndrome (HUS) - diarrhoea negative (2623) Atypical haemolytic uraemic syndrome (HUS) - diarrhoea negative
prd2634 Thrombotic thrombocytopenic purpura (TTP) (2634) Thrombotic thrombocytopenic purpura (TTP)
prd2647 Haemolytic uraemic syndrome (HUS) secondary to systemic disease (2647) Haemolytic uraemic syndrome (HUS) secondary to systemic disease
prd2652 Congenital haemolytic uraemic syndrome (HUS) (2652) Congenital haemolytic uraemic syndrome (HUS)
prd2668 Familial haemolytic uraemic syndrome (HUS) (2668) Familial haemolytic uraemic syndrome (HUS)
prd2675 Familial thrombotic thrombocytopenic purpura (TTP) (2675) Familial thrombotic thrombocytopenic purpura (TTP)
prd2681 Nephropathy due to eclampsia (2681) Nephropathy due to eclampsia
prd2699 Sickle cell nephropathy - no histology (2699) Sickle cell nephropathy - no histology
prd2702 Sickle cell nephropathy - histologically proven (2702) Sickle cell nephropathy - histologically proven
prd2718 Autosomal dominant (AD) polycystic kidney disease (2718) Autosomal dominant (AD) polycystic kidney disease
prd2725 Autosomal dominant (AD) polycystic kidney disease type I (2725) Autosomal dominant (AD) polycystic kidney disease type I
prd2739 Autosomal dominant (AD) polycystic kidney disease type II (2739) Autosomal dominant (AD) polycystic kidney disease type II
prd2741 Autosomal recessive (AR) polycystic kidney disease (2741) Autosomal recessive (AR) polycystic kidney disease
prd2756 Alport syndrome - no histology (2756) Alport syndrome - no histology
prd2760 Alport syndrome - histologically proven (2760) Alport syndrome - histologically proven
prd2773 Benign familial haematuria (2773) Benign familial haematuria
prd2787 Thin basement membrane disease (2787) Thin basement membrane disease
prd2794 Cystic kidney disease (2794) Cystic kidney disease
prd2804 Medullary cystic kidney disease type I (2804) Medullary cystic kidney disease type I
prd2815 Medullary cystic kidney disease type II (2815) Medullary cystic kidney disease type II
prd2827 Uromodulin-associated nephropathy (familial juvenile hyperuricaemic nephropathy) (2827) Uromodulin-associated nephropathy (familial juvenile hyperuricaemic nephropathy)
prd2836 Nephronophthisis (2836) Nephronophthisis
prd2843 Nephronophthisis - type 1 (juvenile type) (2843) Nephronophthisis - type 1 (juvenile type)
prd2858 Nephronophthisis - type 2 (infantile type) (2858) Nephronophthisis - type 2 (infantile type)
prd2862 Nephronophthisis - type 3 (adolescent type) (2862) Nephronophthisis - type 3 (adolescent type)
prd2870 Nephronophthisis - type 4 (juvenile type) (2870) Nephronophthisis - type 4 (juvenile type)
prd2889 Nephronophthisis - type 5 (2889) Nephronophthisis - type 5
prd2891 Nephronophthisis - type 6 (2891) Nephronophthisis - type 6
prd2901 Primary Fanconi syndrome (2901) Primary Fanconi syndrome
prd2917 Tubular disorder as part of inherited metabolic diseases (2917) Tubular disorder as part of inherited metabolic diseases
prd2929 Dent disease (2929) Dent disease
prd2938 Lowe syndrome (oculocerebrorenal syndrome) (2938) Lowe syndrome (oculocerebrorenal syndrome)
prd2940 Inherited aminoaciduria (2940) Inherited aminoaciduria
prd2955 Cystinuria (2955) Cystinuria
prd2964 Cystinosis (2964) Cystinosis
prd2972 Inherited renal glycosuria (2972) Inherited renal glycosuria
prd2986 Hypophosphataemic rickets X-linked (XL) (2986) Hypophosphataemic rickets X-linked (XL)
prd2993 Hypophosphataemic rickets autosomal recessive (AR) (2993) Hypophosphataemic rickets autosomal recessive (AR)
prd3000 Primary renal tubular acidosis (RTA) (3000) Primary renal tubular acidosis (RTA)
prd3016 Proximal renal tubular acidosis (RTA) - type II (3016) Proximal renal tubular acidosis (RTA) - type II
prd3028 Distal renal tubular acidosis (RTA) - type I (3028) Distal renal tubular acidosis (RTA) - type I
prd3037 Distal renal tubular acidosis with sensorineural deafness - gene mutations (3037) Distal renal tubular acidosis with sensorineural deafness - gene mutations
prd3044 Nephrogenic diabetes insipidus (3044) Nephrogenic diabetes insipidus
prd3059 Lesch Nyhan syndrome - hypoxanthine guanine phosphoribosyl transferase deficiency (3059) Lesch Nyhan syndrome - hypoxanthine guanine phosphoribosyl transferase deficiency
prd3063 Phosphoribosyl pyrophosphate synthetase (PRPPS) superactivity (3063) Phosphoribosyl pyrophosphate synthetase (PRPPS) superactivity
prd3071 Alagille syndrome (3071) Alagille syndrome
prd3085 Bartter syndrome (3085) Bartter syndrome
prd3092 Gitelman syndrome (3092) Gitelman syndrome
prd3102 Liddle syndrome (3102) Liddle syndrome
prd3118 Apparent mineralocorticoid excess (3118) Apparent mineralocorticoid excess
prd3125 Glucocorticoid suppressible hyperaldosteronism (3125) Glucocorticoid suppressible hyperaldosteronism
prd3139 Inherited / genetic diabetes mellitus type II (3139) Inherited / genetic diabetes mellitus type II
prd3141 Pseudohypoaldosteronism type 1 (3141) Pseudohypoaldosteronism type 1
prd3156 Pseudohypoaldosteronism type 2 (Gordon syndrome) (3156) Pseudohypoaldosteronism type 2 (Gordon syndrome)
prd3160 Familial hypocalciuric hypercalcaemia (3160) Familial hypocalciuric hypercalcaemia
prd3173 Familial hypercalciuric hypocalcaemia (3173) Familial hypercalciuric hypocalcaemia
prd3187 Familial hypomagnesaemia (3187) Familial hypomagnesaemia
prd3194 Primary hyperoxaluria (3194) Primary hyperoxaluria
prd3207 Primary hyperoxaluria type I (3207) Primary hyperoxaluria type I
prd3211 Primary hyperoxaluria type II (3211) Primary hyperoxaluria type II
prd3224 Fabry disease - no histology (3224) Fabry disease - no histology
prd3230 Fabry disease - histologically proven (3230) Fabry disease - histologically proven
prd3248 Xanthinuria (3248) Xanthinuria
prd3253 Nail-patella syndrome (3253) Nail-patella syndrome
prd3269 Rubinstein-Taybi syndrome (3269) Rubinstein-Taybi syndrome
prd3276 Tuberous sclerosis (3276) Tuberous sclerosis
prd3282 Von Hippel-Lindau disease (3282) Von Hippel-Lindau disease
prd3295 Medullary sponge kidneys (3295) Medullary sponge kidneys
prd3305 Horse-shoe kidney (3305) Horse-shoe kidney
prd3314 Frasier syndrome (3314) Frasier syndrome
prd3322 Branchio-oto-renal syndrome (3322) Branchio-oto-renal syndrome
prd3333 Williams syndrome (3333) Williams syndrome
prd3346 Townes-Brocks syndrome (3346) Townes-Brocks syndrome
prd3351 Lawrence-Moon-Biedl / Bardet-Biedl syndrome (3351) Lawrence-Moon-Biedl / Bardet-Biedl syndrome
prd3367 Mitochondrial cytopathy (3367) Mitochondrial cytopathy
prd3379 Familial nephropathy (3379) Familial nephropathy
prd3380 Acute kidney injury (3380) Acute kidney injury
prd3398 Acute kidney injury due to hypovolaemia (3398) Acute kidney injury due to hypovolaemia
prd3403 Acute kidney injury due to circulatory failure (3403) Acute kidney injury due to circulatory failure
prd3419 Acute kidney injury due to sepsis (3419) Acute kidney injury due to sepsis
prd3426 Acute kidney injury due to rhabdomyolysis (3426) Acute kidney injury due to rhabdomyolysis
prd3435 Acute kidney injury due to nephrotoxicity (3435) Acute kidney injury due to nephrotoxicity
prd3442 Acute cortical necrosis (3442) Acute cortical necrosis
prd3457 Acute pyelonephritis (3457) Acute pyelonephritis
prd3461 Kidney tumour (3461) Kidney tumour
prd3474 Renal cell carcinoma - histologically proven (3474) Renal cell carcinoma - histologically proven
prd3488 Transitional cell carcinoma - histologically proven (3488) Transitional cell carcinoma - histologically proven
prd3490 Wilms tumour - histologically proven (3490) Wilms tumour - histologically proven
prd3501 Mesoblastic nephroma - histologically proven (3501) Mesoblastic nephroma - histologically proven
prd3517 Single kidney identified in adulthood (3517) Single kidney identified in adulthood
prd3529 Chronic kidney disease (CKD) / chronic renal failure (CRF) caused by tumour nephrectomy (3529) Chronic kidney disease (CKD) / chronic renal failure (CRF) caused by tumour nephrectomy
prd3538 Chronic kidney disease (CKD) / chronic renal failure (CRF) due to traumatic loss of kidney (3538) Chronic kidney disease (CKD) / chronic renal failure (CRF) due to traumatic loss of kidney
prd3540 Chronic kidney disease (CKD) / chronic renal failure (CRF) due to donor nephrectomy (3540) Chronic kidney disease (CKD) / chronic renal failure (CRF) due to donor nephrectomy
prd3555 Chronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - no histology (3555) Chronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - no histology
prd3564 Chronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - histologically proven (3564) Chronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - histologically proven
prd3572 Haematuria and proteinuria - no histology (3572) Haematuria and proteinuria - no histology
prd3604 Nephrotic syndrome of childhood - steroid resistant - no histology (3604) Nephrotic syndrome of childhood - steroid resistant - no histology
prd3615 Nephrotic syndrome of childhood - no trial of steroids - no histology (3615) Nephrotic syndrome of childhood - no trial of steroids - no histology
prd3627 Renal cysts and diabetes syndrome (3627) Renal cysts and diabetes syndrome
prd3636 Chronic urate nephropathy - no histology (3636) Chronic urate nephropathy - no histology
prd3643 Chronic renal failure due to systemic infection (3643) Chronic renal failure due to systemic infection
prd3658 Renal coloboma syndrome (3658) Renal coloboma syndrome
prd3662 Hypercalcaemic nephropathy (3662) Hypercalcaemic nephropathy
prd3670 Retroperitoneal fibrosis secondary to peri-aortitis (3670) Retroperitoneal fibrosis secondary to peri-aortitis
prd3689 Retroperitoneal fibrosis secondary to drugs (3689) Retroperitoneal fibrosis secondary to drugs
prd3691 Renal failure (3691) Renal failure
prd3708 Chronic renal failure (3708) Chronic renal failure
prd3712 Isolated haematuria - no histology (3712) Isolated haematuria - no histology
prd3720 Isolated proteinuria - no histology (3720) Isolated proteinuria - no histology
prd3731 Primary hyperoxaluria type III (3731) Primary hyperoxaluria type III
prd3749 Glomerulonephritis - no histology (3749) Glomerulonephritis - no histology
prd3754 Focal segmental glomerulosclerosis (FSGS) secondary to HIV (3754) Focal segmental glomerulosclerosis (FSGS) secondary to HIV
prd3765 Focal segmental glomerulosclerosis (FSGS) secondary to lithium (3765) Focal segmental glomerulosclerosis (FSGS) secondary to lithium
prd3777 Focal segmental glomerulosclerosis (FSGS) secondary to sickle cell (3777) Focal segmental glomerulosclerosis (FSGS) secondary to sickle cell
prd3783 Renal papillary necrosis caused by diabetes (3783) Renal papillary necrosis caused by diabetes
prd3796 Renal papillary necrosis caused by analgesics (3796) Renal papillary necrosis caused by analgesics
prd3806 Renal papillary necrosis caused by sickle cell (3806) Renal papillary necrosis caused by sickle cell
prd3810 Kidney stones due to ARPT deficiency (3810) Kidney stones due to ARPT deficiency
prd3823 Infiltration by lymphoma - histologically proven (3823) Infiltration by lymphoma - histologically proven
prd3834 Nephropathy due to pre-eclampsia (3834) Nephropathy due to pre-eclampsia
prd3847 Systemic vasculitis - ANCA negative - no histology (3847) Systemic vasculitis - ANCA negative - no histology
prd3852 Systemic vasculitis - ANCA positive - histologically proven (3852) Systemic vasculitis - ANCA positive - histologically proven