Types

Complex Types

CF_EDTA_PRD
CodingStandard xs:string (restricted)
Enumeration:
  • EDTA ()
  • EDTA2 ()
  • SNOMED ()
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))
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