Code |
xs:string
(restricted)
Enumeration:
- 0 (Chronic Renal Failure, Aetiology uncertain)
- 10 (Glomerulonephritis, historically not examined)
- 11 (Severe nephoritic syndrome with focal sclerosis (Paediatric))
- 12 (IgA nephropathy proven by immunofluoresence)
- 13 (Dense deposite disease, membrano-prolif. GN Type II)
- 14 (Membranous nephropathy)
- 15 (Membrano-proliferative GN Type I)
- 16 (Rapidly progressive GN without systemic disease (crescentic))
- 17 (Focal segmental glomeruloscerosis with nephrotic syndrome in adults)
- 19 (Glomerulonephritis, historically examined)
- 20 (Pyelo/Interstital nephritis - cause not specified)
- 21 (Pyelo/Interstital nephritis - with neurogenic bladder)
- 22 (Pyelo/Interstital nephritis - congen. obst. uropathy +/- reflux)
- 23 (Pyelo/Interstital nephritis - acquired obst. uropathy)
- 24 (Pyelo/Interstital nephritis - vesico-ureteric reflux no obstruction)
- 25 (Pyelo/Interstital nephritis - due to urolithiasis)
- 29 (Pyelo/Interstital nephritis - due to other cause (please specify))
- 30 (Tubulo interstital nephritis (not pyelonephritis))
- 31 (Nephropathy due to analgesic drugs)
- 32 (Nephropathy due to cis-platinum)
- 33 (Nephropathy due to Cyclosporin A)
- 34 (Lead induced nephropathy (interstitial))
- 39 (Nephroapthy caused by other specific drug)
- 40 (Cystic Kidney Disease - Type Unspecified)
- 41 (Polycystic Kidneys - Adult Type (Dominant))
- 42 (Polycystic Kidneys = Infantile (Recessive))
- 43 (Medullary Cystic Disease - including Nephoronophthisis)
- 49 (Cystic Kidney Disease - Other Specified Type)
- 50 (Hereditary/Familial Nephropathy - Typoe Unspecified)
- 51 (Hereditary Nephritis with Nerve Deafness (Alport's))
- 52 (Cystinosis)
- 53 (Primary Oxalosis)
- 54 (Fabry's disease)
- 59 (Hereditary Nephropathy - Other)
- 60 (congenital Renal Hypoplasia - Type Unspecified)
- 61 (Oligomeganephronic Hypoplasia)
- 63 (Congenital Renal Dysplasia +/- Urinary Tract Malformation)
- 66 (Syndrome of Agenesis of Abdo. muscles - Prune Belly Syndrome)
- 70 (Renal Vascular Disease - Type Unspecified)
- 71 (Renal Vascular Disease due to MALIGNANT Hypertension)
- 72 (Renal Vascular Disease due to Hypertension)
- 73 (Renal Vascular Disease due to Polyarteritis)
- 74 (Wegener's Granulomatosis)
- 75 (Ischaemic Renal Disease/Cholesterol Embolism)
- 76 (Glomerulonephritis related to liver cirrhosis)
- 78 (Cryoglobulinaemic Glomerulonephritis)
- 79 (Renal Vascular Disease - Classified (Please Specify))
- 80 (Diabetes Type 1 (Insulin Dependent))
- 81 (Diabetes Type 2 (Non-Insulin Dependent))
- 82 (Myelomatosis)
- 83 (Amyloid)
- 84 (Systemic Lupus Erythematosus)
- 85 (Henoch-Schonlein Purpura)
- 86 (Goodpastures Syndrome)
- 87 (Scleroderma)
- 88 (Haemolytic Uraemic Syndrome)
- 89 (Multu-System Diseased - Type Unspecified)
- 90 (Cortical or Tubula Necrosis)
- 91 (Tuberculosis)
- 92 (Gout)
- 93 (Nephrocalcinosis / Hypercalcaemic Nephropathy)
- 94 (Balkan Nephropathy)
- 95 (Kidney Tumour)
- 96 (Traumatic or Surgical Loss of Kidney)
- 99 (Other identified Renal Disorders - Please Specify)
- 1003 (Adult Nephrotic Syndrome - No Histology)
- 1019 (Nephrotic Syndrome Of Childhood - Steroid Sensitive - No Histology)
- 1026 (Congenital Nephrotic Syndrome (Cns) - No Histology)
- 1035 (Congenital Nephrotic Syndrome (Cns) - Finnish Type - No Histology)
- 1042 (Congenital Nephrotic Syndrome (Cns) - Finnish Type - Histologically Proven)
- 1057 (Congenital Nephrotic Syndrome (Cns) - Diffuse Mesangial Sclerosis)
- 1061 (Congenital Nephrotic Syndrome (Cns) - Focal Segmental Glomerulosclerosis (Fsgs))
- 1074 (Denys-Drash Syndrome)
- 1088 (Congenital Nephrotic Syndrome (Cns) - Congenital Infection)
- 1090 (Minimal Change Nephropathy - No Histology)
- 1100 (Minimal Change Nephropathy - Histologically Proven)
- 1116 (Iga Nephropathy - No Histology)
- 1128 (Iga Nephropathy - Histologically Proven)
- 1137 (Familial Iga Nephropathy - No Histology)
- 1144 (Familial Iga Nephropathy - Histologically Proven)
- 1159 (Iga Nephropathy Secondary To Liver Cirrhosis - No Histology)
- 1163 (Iga Nephropathy Secondary To Liver Cirrhosis - Histologically Proven)
- 1171 (Igm - Associated Nephropathy)
- 1185 (Membranous Nephropathy - Idiopathic)
- 1192 (Membranous Nephropathy - Malignancy Associated)
- 1205 (Membranous Nephropathy - Drug Induced)
- 1214 (Membranous Nephropathy - Infection Associated)
- 1222 (Mesangiocapillary Glomerulonephritis Type 1)
- 1233 (Mesangiocapillary Glomerulonephritis Type 2 (Dense Deposit Disease))
- 1246 (Mesangiocapillary Glomerulonephritis Type 3)
- 1251 (Idiopathic Rapidly Progressive (Crescentic) Glomerulonephritis)
- 1267 (Primary Focal Segmental Glomerulosclerosis (Fsgs))
- 1279 (Familial Focal Segmental Glomerulosclerosis (Fsgs) - Autosomal Recessive - No Histology)
- 1280 (Familial Focal Segmental Glomerulosclerosis (Fsgs) - Autosomal Recessive - Histologically Proven)
- 1298 (Familial Focal Segmental Glomerulosclerosis (Fsgs) - Autosomal Dominant - No Histology)
- 1308 (Familial Focal Segmental Glomerulosclerosis (Fsgs) - Autosomal Dominant - Histologically Proven)
- 1312 (Focal Segmental Glomerulosclerosis (Fsgs) Secondary To Obesity - No Histology)
- 1320 (Focal Segmental Glomerulosclerosis (Fsgs) Secondary To Obesity - Histologically Proven)
- 1331 (Diffuse Endocapillary Glomerulonephritis)
- 1349 (Mesangial Proliferative Glomerulonephritis)
- 1354 (Focal And Segmental Proliferative Glomerulonephritis)
- 1365 (Glomerulonephritis - Secondary To Other Systemic Disease)
- 1377 (Glomerulonephritis - Histologically Indeterminate)
- 1383 (Systemic Vasculitis - Anca Negative - Histologically Proven)
- 1396 (Systemic Vasculitis - Anca Positive - No Histology)
- 1401 (Granulomatosis With Polyangiitis - No Histology)
- 1417 (Granulomatosis With Polyangiitis - Histologically Proven)
- 1429 (Microscopic Polyangiitis - Histologically Proven)
- 1438 (Churg-Strauss Syndrome - No Histology)
- 1440 (Churg-Strauss Syndrome - Histologically Proven)
- 1455 (Polyarteritis Nodosa)
- 1464 (Anti-Glomerular Basement Membrane (Gbm) Disease / Goodpasture'S Syndrome - No Histology)
- 1472 (Anti-Glomerular Basement Membrane (Gbm) Disease / Goodpasture'S Syndrome - Histologically Proven)
- 1486 (Systemic Lupus Erythematosus / Nephritis - No Histology)
- 1493 (Systemic Lupus Erythematosus / Nephritis - Histologically Proven)
- 1504 (Henoch-Schonlein Purpura / Nephritis - No Histology)
- 1515 (Henoch-Schonlein Purpura / Nephritis - Histologically Proven)
- 1527 (Renal Scleroderma / Systemic Sclerosis - No Histology)
- 1536 (Renal Scleroderma / Systemic Sclerosis - Histologically Proven)
- 1543 (Essential Mixed Cryoglobulinaemia - No Histology)
- 1558 (Essential Mixed Cryoglobulinaemia - Histologically Proven)
- 1562 (Cryoglobulinaemia Secondary To Hepatitis C - No Histology)
- 1570 (Cryoglobulinaemia Secondary To Hepatitis C - Histologically Proven)
- 1589 (Cryoglobulinaemia Secondary To Systemic Disease - No Histology)
- 1591 (Cryoglobulinaemia Secondary To Systemic Disease - Histologically Proven)
- 1602 (Primary Reflux Nephropathy - Sporadic)
- 1618 (Familial Reflux Nephropathy)
- 1625 (Congenital Dysplasia / Hypoplasia)
- 1639 (Multicystic Dysplastic Kidneys)
- 1641 (Dysplasia Due To Fetal Ace-Inhibitor Exposure)
- 1656 (Glomerulocystic Disease)
- 1660 (Congenital Pelvi-Ureteric Junction Obstruction)
- 1673 (Congenital Vesico-Ureteric Junction Obstruction)
- 1687 (Posterior Urethral Valves)
- 1694 (Syndrome Of Agenesis Of Abdominal Muscles - Prune Belly Syndrome)
- 1706 (Congenital Neurogenic Bladder)
- 1710 (Bladder Exstrophy)
- 1723 (Megacystis-Megaureter)
- 1734 (Oligomeganephronia)
- 1747 (Renal Papillary Necrosis - Cause Unknown)
- 1752 (Acquired Obstructive Uropathy / Nephropathy)
- 1768 (Acquired Obstructive Nephropathy Due To Neurogenic Bladder)
- 1775 (Obstructive Nephropathy Due To Prostatic Hypertrophy)
- 1781 (Obstructive Nephropathy Due To Prostate Cancer)
- 1799 (Obstructive Nephropathy Due To Bladder Cancer)
- 1809 (Obstructive Nephropathy Due To Other Malignancies)
- 1813 (Idiopathic Retroperitoneal Fibrosis)
- 1821 (Retroperitoneal Fibrosis Secondary To Malignancies)
- 1832 (Calculus Nephropathy / Urolithiasis)
- 1845 (Calcium Oxalate Urolithiasis)
- 1850 (Enteric Hyperoxaluria)
- 1866 (Magnesium Ammonium Phosphate (Struvite) Urolithiasis)
- 1878 (Uric Acid Urolithiasis)
- 1884 (Tubulointerstitial Nephritis - No Histology)
- 1897 (Tubulointerstitial Nephritis - Histologically Proven)
- 1907 (Familial Interstitial Nephropathy - No Histology)
- 1911 (Familial Interstitial Nephropathy - Histologically Proven)
- 1924 (Tubulointerstitial Nephritis Associated With Autoimmune Disease - No Histology)
- 1930 (Tubulointerstitial Nephritis Associated With Autoimmune Disease - Histologically Proven)
- 1948 (Tubulointerstitial Nephritis With Uveitis (Tinu) - No Histology)
- 1953 (Tubulointerstitial Nephritis With Uveitis (Tinu) - Histologically Proven)
- 1969 (Renal Sarcoidosis - No Histology)
- 1976 (Renal Sarcoidosis - Histologically Proven)
- 1982 (Aristolochic Acid Nephropathy (Balkan / Chinese Herb / Endemic Nephropathy) - No Histology)
- 1995 (Aristolochic Acid Nephropathy (Balkan / Chinese Herb / Endemic Nephropathy) - Histologically Proven)
- 2005 (Drug-Induced Tubulointerstitial Nephritis - No Histology)
- 2014 (Drug-Induced Tubulointerstitial Nephritis - Histologically Proven)
- 2022 (Nephropathy Due To Analgesic Drugs - No Histology)
- 2033 (Nephropathy Due To Analgesic Drugs - Histologically Proven)
- 2046 (Nephropathy Due To Ciclosporin - No Histology)
- 2051 (Nephropathy Due To Ciclosporin - Histologically Proven)
- 2067 (Nephropathy Due To Tacrolimus - No Histology)
- 2079 (Nephropathy Due To Tacrolimus - Histologically Proven)
- 2080 (Nephropathy Due To Aminoglycosides - No Histology)
- 2098 (Nephropathy Due To Aminoglycosides - Histologically Proven)
- 2108 (Nephropathy Due To Amphotericin - No Histology)
- 2112 (Nephropathy Due To Amphotericin - Histologically Proven)
- 2120 (Nephropathy Due To Cisplatin - No Histology)
- 2131 (Nephropathy Due To Cisplatin - Histologically Proven)
- 2149 (Nephropathy Due To Lithium - No Histology)
- 2154 (Nephropathy Due To Lithium - Histologically Proven)
- 2165 (Lead Induced Nephropathy - No Histology)
- 2177 (Lead Induced Nephropathy - Histologically Proven)
- 2183 (Acute Urate Nephropathy - No Histology)
- 2196 (Acute Urate Nephropathy - Histologically Proven)
- 2203 (Chronic Urate Nephropathy - Histologically Proven)
- 2219 (Radiation Nephritis)
- 2226 (Renal / Perinephric Abscess)
- 2235 (Renal Tuberculosis)
- 2242 (Leptospirosis)
- 2257 (Hantavirus Nephropathy)
- 2261 (Xanthogranulomatous Pyelonephritis)
- 2274 (Nephropathy Related To Hiv - No Histology)
- 2288 (Nephropathy Related To Hiv - Histologically Proven)
- 2290 (Schistosomiasis)
- 2300 (Other Specific Infection)
- 2316 (Diabetic Nephropathy In Type I Diabetes - No Histology)
- 2328 (Diabetic Nephropathy In Type I Diabetes - Histologically Proven)
- 2337 (Diabetic Nephropathy In Type Ii Diabetes - No Histology)
- 2344 (Diabetic Nephropathy In Type Ii Diabetes - Histologically Proven)
- 2359 (Chronic Hypertensive Nephropathy - No Histology)
- 2363 (Chronic Hypertensive Nephropathy - Histologically Proven)
- 2371 (Malignant Hypertensive Nephropathy / Accelerated Hypertensive Nephropathy - No Histology)
- 2385 (Malignant Hypertensive Nephropathy / Accelerated Hypertensive Nephropathy - Histologically Proven)
- 2392 (Ageing Kidney - No Histology)
- 2407 (Ischaemic Nephropathy - No Histology)
- 2411 (Ischaemic Nephropathy / Microvascular Disease - Histologically Proven)
- 2424 (Renal Artery Stenosis)
- 2430 (Atheroembolic Renal Disease - No Histology)
- 2448 (Atheroembolic Renal Disease - Histologically Proven)
- 2453 (Fibromuscular Dysplasia Of Renal Artery)
- 2469 (Renal Arterial Thrombosis / Occlusion)
- 2476 (Renal Vein Thrombosis)
- 2482 (Cardiorenal Syndrome)
- 2495 (Hepatorenal Syndrome)
- 2509 (Renal Amyloidosis)
- 2513 (Aa Amyloid Secondary To Chronic Inflammation)
- 2521 (Al Amyloid Secondary To Plasma Cell Dyscrasia)
- 2532 (Familial Amyloid Secondary To Protein Mutations - No Histology)
- 2545 (Familial Amyloid Secondary To Protein Mutations - Histologically Proven)
- 2550 (Familial Aa Amyloid Secondary To Familial Mediterranean Fever / Traps (Hibernian Fever) - No Histology)
- 2566 (Familial Aa Amyloid Secondary To Familial Mediterranean Fever / Traps (Hibernian Fever) - Histologically Proven)
- 2578 (Myeloma Kidney - No Histology)
- 2584 (Myeloma Cast Nephropathy - Histologically Proven)
- 2597 (Light Chain Deposition Disease)
- 2606 (Immunotactoid / Fibrillary Nephropathy)
- 2610 (Haemolytic Uraemic Syndrome (Hus) - Diarrhoea Associated)
- 2623 (Atypical Haemolytic Uraemic Syndrome (Hus) - Diarrhoea Negative)
- 2634 (Thrombotic Thrombocytopenic Purpura (Ttp))
- 2647 (Haemolytic Uraemic Syndrome (Hus) Secondary To Systemic Disease)
- 2652 (Congenital Haemolytic Uraemic Syndrome (Hus))
- 2668 (Familial Haemolytic Uraemic Syndrome (Hus))
- 2675 (Familial Thrombotic Thrombocytopenic Purpura (Ttp))
- 2681 (Nephropathy Due To Pre-Eclampsia / Eclampsia)
- 2699 (Sickle Cell Nephropathy - No Histology)
- 2702 (Sickle Cell Nephropathy - Histologically Proven)
- 2718 (Autosomal Dominant (Ad) Polycystic Kidney Disease)
- 2725 (Autosomal Dominant (Ad) Polycystic Kidney Disease Type I)
- 2739 (Autosomal Dominant (Ad) Polycystic Kidney Disease Type Ii)
- 2741 (Autosomal Recessive (Ar) Polycystic Kidney Disease)
- 2756 (Alport Syndrome - No Histology)
- 2760 (Alport Syndrome - Histologically Proven)
- 2773 (Benign Familial Haematuria)
- 2787 (Thin Basement Membrane Disease)
- 2794 (Cystic Kidney Disease)
- 2804 (Medullary Cystic Kidney Disease Type I)
- 2815 (Medullary Cystic Kidney Disease Type Ii)
- 2827 (Uromodulin-Associated Nephropathy (Familial Juvenile Hyperuricaemic Nephropathy))
- 2836 (Nephronophthisis)
- 2843 (Nephronophthisis - Type 1 (Juvenile Type))
- 2858 (Nephronophthisis - Type 2 (Infantile Type))
- 2862 (Nephronophthisis - Type 3 (Adolescent Type))
- 2870 (Nephronophthisis - Type 4 (Juvenile Type))
- 2889 (Nephronophthisis - Type 5)
- 2891 (Nephronophthisis - Type 6)
- 2901 (Primary Fanconi Syndrome)
- 2917 (Tubular Disorder As Part Of Inherited Metabolic Diseases)
- 2929 (Dent Disease)
- 2938 (Lowe Syndrome (Oculocerebrorenal Syndrome))
- 2940 (Inherited Aminoaciduria)
- 2955 (Cystinuria)
- 2964 (Cystinosis)
- 2972 (Inherited Renal Glycosuria)
- 2986 (Hypophosphataemic Rickets X-Linked (Xl))
- 2993 (Hypophosphataemic Rickets Autosomal Recessive (Ar))
- 3000 (Primary Renal Tubular Acidosis (Rta))
- 3016 (Proximal Renal Tubular Acidosis (Rta) - Type Ii)
- 3028 (Distal Renal Tubular Acidosis (Rta) - Type I)
- 3037 (Distal Renal Tubular Acidosis With Sensorineural Deafness - Gene Mutations)
- 3044 (Nephrogenic Diabetes Insipidus)
- 3059 (Lesch Nyhan Syndrome - Hypoxanthine Guanine Phosphoribosyl Transferase Deficiency)
- 3063 (Phosphoribosyl Pyrophosphate Synthetase (Prpps) Superactivity)
- 3071 (Alagille Syndrome)
- 3085 (Bartter Syndrome)
- 3092 (Gitelman Syndrome)
- 3102 (Liddle Syndrome)
- 3118 (Apparent Mineralocorticoid Excess)
- 3125 (Glucocorticoid Suppressible Hyperaldosteronism)
- 3139 (Inherited / Genetic Diabetes Mellitus Type Ii)
- 3141 (Pseudohypoaldosteronism Type 1)
- 3156 (Pseudohypoaldosteronism Type 2 (Gordon Syndrome))
- 3160 (Familial Hypocalciuric Hypercalcaemia)
- 3173 (Familial Hypercalciuric Hypocalcaemia)
- 3187 (Familial Hypomagnesaemia)
- 3194 (Primary Hyperoxaluria)
- 3207 (Primary Hyperoxaluria Type I)
- 3211 (Primary Hyperoxaluria Type Ii)
- 3224 (Fabry Disease - No Histology)
- 3230 (Fabry Disease - Histologically Proven)
- 3248 (Xanthinuria)
- 3253 (Nail-Patella Syndrome)
- 3269 (Rubinstein-Taybi Syndrome)
- 3276 (Tuberous Sclerosis)
- 3282 (Von Hippel-Lindau Disease)
- 3295 (Medullary Sponge Kidneys)
- 3305 (Horse-Shoe Kidney)
- 3314 (Frasier Syndrome)
- 3322 (Branchio-Oto-Renal Syndrome)
- 3333 (Williams Syndrome)
- 3346 (Townes-Brocks Syndrome)
- 3351 (Lawrence-Moon-Biedl / Bardet-Biedl Syndrome)
- 3367 (Mitochondrial Cytopathy)
- 3379 (Familial Nephropathy)
- 3380 (Acute Kidney Injury)
- 3398 (Acute Kidney Injury Due To Hypovolaemia)
- 3403 (Acute Kidney Injury Due To Circulatory Failure)
- 3419 (Acute Kidney Injury Due To Sepsis)
- 3426 (Acute Kidney Injury Due To Rhabdomyolysis)
- 3435 (Acute Kidney Injury Due To Nephrotoxicity)
- 3442 (Acute Cortical Necrosis)
- 3457 (Acute Pyelonephritis)
- 3461 (Kidney Tumour)
- 3474 (Renal Cell Carcinoma - Histologically Proven)
- 3488 (Transitional Cell Carcinoma - Histologically Proven)
- 3490 (Wilms Tumour - Histologically Proven)
- 3501 (Mesoblastic Nephroma - Histologically Proven)
- 3517 (Single Kidney Identified In Adulthood)
- 3529 (Chronic Kidney Disease (Ckd) / Chronic Renal Failure (Crf) Caused By Tumour Nephrectomy)
- 3538 (Chronic Kidney Disease (Ckd) / Chronic Renal Failure (Crf) Due To Traumatic Loss Of Kidney)
- 3540 (Chronic Kidney Disease (Ckd) / Chronic Renal Failure (Crf) Due To Donor Nephrectomy)
- 3555 (Chronic Kidney Disease (Ckd) / Chronic Renal Failure (Crf) - Aetiology Uncertain / Unknown - No Histology)
- 3564 (Chronic Kidney Disease (Ckd) / Chronic Renal Failure (Crf) - Aetiology Uncertain / Unknown - Histologically Proven)
- 3572 (Haematuria And Proteinuria - No Histology)
- 3604 (Nephrotic Syndrome Of Childhood - Steroid Resistant - No Histology)
- 3615 (Nephrotic Syndrome Of Childhood - No Trial Of Steroids - No Histology)
- 3627 (Renal Cysts And Diabetes Syndrome)
- 3636 (Chronic Urate Nephropathy - No Histology)
- 3643 (Chronic Renal Failure Due To Systemic Infection)
- 3658 (Renal Coloboma Syndrome)
- 3662 (Hypercalcaemic Nephropathy)
- 3670 (Retroperitoneal Fibrosis Secondary To Peri-Aortitis)
- 3689 (Retroperitoneal Fibrosis Secondary To Drugs)
- 3691 (Renal Failure)
- 3708 (Chronic Renal Failure)
- 3712 (Isolated Haematuria - No Histology)
- 3720 (Isolated Proteinuria - No Histology)
- 3731 (Primary Hyperoxaluria Type Iii)
- 3749 (Glomerulonephritis - No Histology)
- 3754 (Focal segmental glomerulosclerosis (FSGS) secondary to HIV)
- 3765 (Focal segmental glomerulosclerosis (FSGS) secondary to lithium)
- 3777 (Focal segmental glomerulosclerosis (FSGS) secondary to sickle cell)
- 3783 (Renal papillary necrosis caused by diabetes)
- 3796 (Renal papillary necrosis caused by analgesics)
- 3806 (Renal papillary necrosis caused by sickle cell)
- 3810 (Kidney stones due to ARPT deficiency)
- 3823 (Infiltration by lymphoma - histologically proven)
- 3834 (Nephropathy due to pre-eclampsia)
- 3847 (Systemic vasculitis - ANCA negative - no histology)
- 3852 (Systemic vasculitis - ANCA positive - histologically proven)
- 36171008 (Glomerulonephritis (disorder))
- 52254009 (Nephrotic syndrome (disorder))
- 445119005 (Steroid sensitive nephrotic syndrome of childhood (disorder))
- 449820008 (Steroid resistant nephrotic syndrome of childhood (disorder))
- 705065000 (Childhood nephrotic syndrome (disorder))
- 48796009 (Congenital nephrotic syndrome (disorder))
- 197601003 (Finnish congenital nephrotic syndrome (disorder))
- 722369003 (Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder))
- 236384008 (Congenital nephrotic syndrome with focal glomerulosclerosis (disorder))
- 236385009 (Drash syndrome (disorder))
- 722118005 (Congenital nephrotic syndrome due to congenital infection (disorder))
- 44785005 (Minimal change disease (disorder))
- 236407003 (Immunoglobulin A nephropathy (disorder))
- 445404003 (Familial immunoglobulin A nephropathy (disorder))
- 282364005 (Immunoglobulin A nephropathy associated with liver disease (disorder))
- 236411009 (Immunoglobulin M nephropathy (disorder))
- 722119002 (Idiopathic membranous glomerulonephritis (disorder))
- 722086002 (Membranous glomerulonephritis due to malignant neoplastic disease (disorder))
- 722120008 (Membranous glomerulonephritis caused by drug (disorder))
- 722168002 (Membranous glomerulonephritis co-occurrent with infectious disease (disorder))
- 75888001 (Mesangiocapillary glomerulonephritis, type I (disorder))
- 59479006 (Mesangiocapillary glomerulonephritis, type II (disorder))
- 236409000 (Mesangiocapillary glomerulonephritis type III (disorder))
- 236398000 (Crescentic glomerulonephritis (disorder))
- 236403004 (Focal segmental glomerulosclerosis (disorder))
- 445388002 (Autosomal recessive focal segmental glomerulosclerosis (disorder))
- 445388002 (Autosomal recessive focal segmental glomerulosclerosis (disorder))
- 444977005 (Autosomal dominant focal segmental glomerulosclerosis (disorder))
- 444977005 (Autosomal dominant focal segmental glomerulosclerosis (disorder))
- 236403004 (Focal segmental glomerulosclerosis (disorder))
- 713887002 (FSGS co-occurrent with human immunodefiency virus infection (disorder))
- 722139003 (Focal segmental glomerulosclerosis caused by lithium (disorder))
- 722147003 (Focal segmental glomerulosclerosis due to sickle cell disease (disorder))
- 3704008 (Diffuse endocapillary proliferative glomerulonephritis (disorder))
- 35546006 (Mesangial proliferative glomerulonephritis (disorder))
- 83866005 (Focal AND segmental proliferative glomerulonephritis (disorder))
- 36171008 (Glomerulonephritis (disorder))
- 46956008 (Systemic vasculitis (disorder))
- 195353004 (Wegener's granulomatosis (disorder))
- 239928004 (Microscopic polyarteritis nodosa (disorder))
- 82275008 (Allergic granulomatosis angiitis (disorder))
- 155441006 (Polyarteritis nodosa (disorder))
- 236506009 (Goodpasture's disease (disorder))
- 50581000 (Goodpasture's syndrome (disorder))
- 68815009 (Systemic lupus erythematosus glomerulonephritis syndrome (disorder))
- 68815009 (Systemic lupus erythematosus glomerulonephritis syndrome (disorder))
- 191306005 (Henoch-Schönlein purpura (disorder))
- 236502006 (Renal involvement in scleroderma (disorder))
- 239947001 (Essential mixed cryoglobulinemia (disorder))
- 239947001 (Essential mixed cryoglobulinemia (disorder))
- 128971000119101 (Cryoglobulinemia due to chronic hepatitis C (disorder))
- 28807005 (Secondary cryoglobulinemia (disorder))
- 197764002 (Non-obstructive reflux-associated chronic pyelonephritis (disorder))
- 707208009 (Familial non-obstructive reflux-associated chronic pyelonephritis (disorder))
- 204949001 (Renal dysplasia (disorder))
- 737562008 (Multicystic renal dysplasia (disorder))
- 710571007 (Renal dysplasia due to fetal exposure to angiotensin converting enzyme inhibitor (disorder))
- 609572000 (Maturity-onset diabetes of the young, type 5 (disorder))
- 253864004 (Familial hypoplastic, glomerulocystic kidney (disorder))
- 373584008 (Congenital pelviureteric junction obstruction (disorder))
- 373585009 (Congenital ureterovesical obstruction (disorder))
- 253900005 (Congenital posterior urethral valves (disorder))
- 5187006 (Prune belly syndrome (disorder))
- 445387007 (Congenital neurogenic urinary bladder (finding))
- 61758007 (Exstrophy of bladder sequence (disorder))
- 253904001 (Megacystis-megaureter syndrome (disorder))
- 18417009 (Oligomeganephronic hypoplasia of kidney (disorder))
- 90241004 (Papillary necrosis (disorder))
- 723074006 (Renal papillary necrosis due to diabetes mellitus (disorder))
- 722077007 (Renal papillary necrosis caused by analgesic drug (disorder))
- 722085003 (Renal papillary necrosis due to sickle cell disease (disorder))
- 698757009 (Nephropathy due to acquired urinary tract obstruction (disorder))
- 722078002 (Obstructive nephropathy due to neurogenic bladder (disorder))
- 722082000 (Obstructive nephropathy due to benign prostatic hyperplasia (disorder))
- 722081007 (Obstructive nephropathy due to carcinoma of prostate (disorder))
- 722089009 (Obstructive nephropathy due to bladder cancer (disorder))
- 722088001 (Obstructive nephropathy due to malignancy (disorder))
- 197808006 (Idiopathic retroperitoneal fibrosis (disorder))
- 236017004 (Malignant retroperitoneal fibrosis (disorder))
- 236015007 (Drug-induced retroperitoneal fibrosis (disorder))
- 49120005 (Retroperitoneal fibrosis (disorder))
- 95566004 (Urolithiasis (disorder))
- 444717006 (Calcium oxalate urolithiasis (disorder))
- 37497004 (Enteric hyperoxaluria (disorder))
- 444690001 (Magnesium ammonium phosphate urolithiasis (disorder))
- 267441009 (Uric acid urolithiasis (disorder))
- 28689008 (Interstitial nephritis (disorder))
- 428255004 (Tubulointerstitial nephritis (disorder))
- 37061001 (Granulomatous sarcoid nephropathy (disorder))
- 236514003 (Toxic nephropathy (disorder))
- 439990003 (Drug-induced interstitial nephritis (disorder))
- 59400006 (Analgesic nephropathy (disorder))
- 704203009 (Nephropathy induced by ciclosporin (disorder))
- 704205002 (Nephropathy induced by tacrolimus (disorder))
- 704206001 (Nephropathy induced by aminoglycoside (disorder))
- 704055002 (Nephropathy induced by amphotericin (disorder))
- 53556002 (Cis-platinum nephropathy (disorder))
- 4390004 (Lithium nephropathy (disorder))
- 704204003 (Nephropathy induced by lead (disorder))
- 236496000 (Acute urate nephropathy (disorder))
- 190829000 (Chronic urate nephropathy (disorder))
- 33763006 (Hypercalcemic nephropathy (disorder))
- 7725007 (Radiation nephritis (disorder))
- 3321001 (Renal abscess (disorder))
- 80640009 (Perirenal abscess (disorder))
- 44323002 (Tuberculosis of kidney (disorder))
- 77377001 (Leptospirosis (disorder))
- 102455002 (Hemorrhagic nephroso-nephritis (disorder))
- 38898003 (Xanthogranulomatous pyelonephritis (disorder))
- 713504001 (Disorder of kidney co-occurrent with human immunodeficiency virus infection (disorder))
- 236706006 (Urinary schistosomiasis (disorder))
- 40733004 (Infectious disease (disorder))
- 421893009 (Renal disorder associated with type I diabetes mellitus (disorder))
- 420279001 (Renal disorder due to type 2 diabetes mellitus (disorder))
- 38481006 (Hypertensive renal disease (disorder))
- 65443008 (Malignant hypertensive renal disease (disorder))
- 65443008 (Malignant hypertensive renal disease (disorder))
- 445108007 (Age related reduction of renal function (finding))
- 710565001 (Nephropathy due to ischemia (disorder))
- 302233006 (Renal artery stenosis (disorder))
- 51677000 (Atheroembolism of renal arteries (disorder))
- 51677000 (Atheroembolism of renal arteries (disorder))
- 2900003 (Hyperplasia of renal artery (disorder))
- 236488005 (Renal artery occlusion (disorder))
- 15842009 (Thrombosis of renal vein (disorder))
- 445236007 (Cardiorenal syndrome (disorder))
- 51292008 (Hepatorenal syndrome (disorder))
- 48713002 (Amyloid nephropathy (disorder))
- 274945004 (AA amyloidosis (disorder))
- 23132008 (AL amyloidosis (disorder))
- 66451004 (Familial visceral amyloidosis, Ostertag type (disorder))
- 367528006 (Amyloid of familial Mediterranean fever (disorder))
- 32278006 (Myeloma kidney (disorder))
- 373604002 (Light chain deposition disease (disorder))
- 73305009 (Fibrillary glomerulonephritis (disorder))
- 373421000 (Diarrhea-associated hemolytic uremic syndrome (disorder))
- 373422007 (Diarrhea-negative hemolytic uremic syndrome (disorder))
- 78129009 (Thrombotic thrombocytopenic purpura (disorder))
- 111407006 (Hemolytic uremic syndrome (disorder))
- 444976001 (Congenital hemolytic uremic syndrome (disorder))
- 722721004 (Familial hemolytic uremic syndrome (disorder))
- 373420004 (Upshaw-Schulman syndrome (disorder))
- 736993008 (Nephropathy following eclampsia (disorder))
- 736992003 (Nephropathy following pre-eclampsia (disorder))
- 13886001 (Sickle cell nephropathy (disorder))
- 28728008 (Polycystic kidney disease, adult type (disorder))
- 253878003 (Adult type polycystic kidney disease type 1 (disorder))
- 253879006 (Adult type polycystic kidney disease type 2 (disorder))
- 28770003 (Polycystic kidney disease, infantile type (disorder))
- 399340005 (Hereditary nephritis (disorder))
- 236421001 (Benign familial hematuria (disorder))
- 236418003 (Thin basement membrane disease (disorder))
- 236439005 (Cystic disease of kidney (disorder))
- 726017001 (Mucin 1 related autosomal dominant tubulointerstitial kidney disease (disorder))
- 723373006 (Autosomal dominant medullary cystic kidney disease with hyperuricemia (disorder))
- 46785007 (Familial juvenile gout (disorder))
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- 444830001 (Juvenile nephronophthisis (disorder))
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- 446991001 (Nephronophthisis type 5 (disorder))
- 447335007 (Nephronophthisis type 6 (disorder))
- 236466005 (Congenital Fanconi syndrome (disorder))
- 197744007 (Renal tubulo-interstitial disorders in metabolic diseases (disorder))
- 444645005 (Dent's disease (disorder))
- 79385002 (Lowe syndrome (disorder))
- 698953004 (Inherited aminoaciduria (disorder))
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- 82236004 (Familial x-linked hypophosphatemic vitamin D refractory rickets (disorder))
- 90505000 (Autosomal recessive hypophosphatemic vitamin D refractory rickets (disorder))
- 1776003 (Renal tubular acidosis (disorder))
- 24790002 (Proximal renal tubular acidosis (disorder))
- 236461000 (Distal renal tubular acidosis (disorder))
- 722468005 (Distal renal tubular acidosis co-occurrent with sensorineural deafness (disorder))
- 111395007 (Nephrogenic diabetes insipidus (disorder))
- 10406007 (Lesch-Nyhan syndrome (disorder))
- 35759001 (Ribose-phosphate pyrophosphokinase overactivity (disorder))
- 124274002 (Deficiency of adenine phosphoribosyl transferase (disorder))
- 31742004 (Arteriohepatic dysplasia (disorder))
- 707742001 (Bartter syndrome (disorder))
- 707756004 (Gitelman syndrome (disorder))
- 707747007 (Pseudoprimary hyperaldosteronism (disorder))
- 237770005 (Syndrome of apparent mineralocorticoid excess (disorder))
- 237743003 (Glucocorticoid-suppressible hyperaldosteronism (disorder))
- 237604008 (Maturity onset diabetes of the young, type 2 (disorder))
- 43941006 (Pseudohypoaldosteronism, type 1 (disorder))
- 15689008 (Pseudohypoaldosteronism, type 2 (disorder))
- 237885008 (Familial hypocalciuric hypercalcemia (disorder))
- 711152006 (Autosomal dominant hypocalcemia (disorder))
- 80710001 (Primary hypomagnesemia (disorder))
- 17901006 (Primary hyperoxaluria (disorder))
- 65520001 (Primary hyperoxaluria, type I (disorder))
- 40951006 (Primary hyperoxaluria, type II (disorder))
- 734990008 (Primary hyperoxaluria, type III (disorder))
- 16652001 (Fabry's disease (disorder))
- 190919008 (Xanthinuria (disorder))
- 236527004 (Nail patella-like renal disease (disorder))
- 45582004 (Rubinstein-Taybi syndrome (disorder))
- 7199000 (Tuberous sclerosis syndrome (disorder))
- 46659004 (Von Hippel-Lindau syndrome (disorder))
- 236443009 (Medullary sponge kidney (disorder))
- 41729002 (Horseshoe kidney (disorder))
- 445431000 (Frasier syndrome (disorder))
- 446449009 (Renal coloboma syndrome (disorder))
- 290006 (Melnick-Fraser syndrome (disorder))
- 63247009 (Williams syndrome (disorder))
- 24750000 (Townes syndrome (disorder))
- 232059000 (Laurence-Moon syndrome (disorder))
- 240096000 (Mitochondrial cytopathy (disorder))
- 236419006 (Progressive hereditary glomerulonephritis without deafness (disorder))
- 14669001 (Acute renal failure syndrome (disorder))
- 722096006 (Acute kidney injury due to hypovolemia (disorder))
- 722095005 (Acute kidney injury due to circulatory failure (disorder))
- 722278006 (Acute kidney injury due to sepsis (disorder))
- 23697004 (Crush syndrome (disorder))
- 236428007 (Nephrotoxic acute renal failure (disorder))
- 444794000 (Acute necrosis of cortex of kidney (disorder))
- 36689008 (Acute pyelonephritis (disorder))
- 126880001 (Neoplasm of kidney (disorder))
- 254915003 (Clear cell carcinoma of kidney (disorder))
- 408642003 (Transitional cell carcinoma of kidney (disorder))
- 302849000 (Nephroblastoma (disorder))
- 307604008 (Mesoblastic nephroma (disorder))
- 236513009 (Lymphomatous infiltrate of kidney)
- 249582007 (Absent kidney (finding))
- 722149000 (Chronic kidney disease following excision of renal neoplasm (disorder))
- 722467000 (Chronic kidney disease due to traumatic loss of kidney (disorder))
- 722098007 (Chronic kidney disease following donor nephrectomy (disorder))
- 90688005 (Chronic renal failure syndrome (disorder))
- 53298000 (Hematuria syndrome (disorder))
- 29738008 (Proteinuria (finding))
- 722150000 (Chronic kidney disease due to systemic infection (disorder))
- 42399005 (Renal failure syndrome (disorder))
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