Chronic Renal Failure, Aetiology uncertain Glomerulonephritis, historically not examined Severe nephoritic syndrome with focal sclerosis (Paediatric) IgA nephropathy proven by immunofluoresence Dense deposite disease, membrano-prolif. GN Type II Membranous nephropathy Membrano-proliferative GN Type I Rapidly progressive GN without systemic disease (crescentic) Focal segmental glomeruloscerosis with nephrotic syndrome in adults Glomerulonephritis, historically examined Pyelo/Interstital nephritis - cause not specified Pyelo/Interstital nephritis - with neurogenic bladder Pyelo/Interstital nephritis - congen. obst. uropathy +/- reflux Pyelo/Interstital nephritis - acquired obst. uropathy Pyelo/Interstital nephritis - vesico-ureteric reflux no obstruction Pyelo/Interstital nephritis - due to urolithiasis Pyelo/Interstital nephritis - due to other cause (please specify) Tubulo interstital nephritis (not pyelonephritis) Nephropathy due to analgesic drugs Nephropathy due to cis-platinum Nephropathy due to Cyclosporin A Lead induced nephropathy (interstitial) Nephroapthy caused by other specific drug Cystic Kidney Disease - Type Unspecified Polycystic Kidneys - Adult Type (Dominant) Polycystic Kidneys = Infantile (Recessive) Medullary Cystic Disease - including Nephoronophthisis Cystic Kidney Disease - Other Specified Type Hereditary/Familial Nephropathy - Typoe Unspecified Hereditary Nephritis with Nerve Deafness (Alport's) Cystinosis Primary Oxalosis Fabry's disease Hereditary Nephropathy - Other congenital Renal Hypoplasia - Type Unspecified Oligomeganephronic Hypoplasia Congenital Renal Dysplasia +/- Urinary Tract Malformation Syndrome of Agenesis of Abdo. muscles - Prune Belly Syndrome Renal Vascular Disease - Type Unspecified Renal Vascular Disease due to MALIGNANT Hypertension Renal Vascular Disease due to Hypertension Renal Vascular Disease due to Polyarteritis Wegener's Granulomatosis Ischaemic Renal Disease/Cholesterol Embolism Glomerulonephritis related to liver cirrhosis Cryoglobulinaemic Glomerulonephritis Renal Vascular Disease - Classified (Please Specify) Diabetes Type 1 (Insulin Dependent) Diabetes Type 2 (Non-Insulin Dependent) Myelomatosis Amyloid Systemic Lupus Erythematosus Henoch-Schonlein Purpura Goodpastures Syndrome Scleroderma Haemolytic Uraemic Syndrome Multu-System Diseased - Type Unspecified Cortical or Tubula Necrosis Tuberculosis Gout Nephrocalcinosis / Hypercalcaemic Nephropathy Balkan Nephropathy Kidney Tumour Traumatic or Surgical Loss of Kidney Other identified Renal Disorders - Please Specify Adult Nephrotic Syndrome - No Histology Nephrotic Syndrome Of Childhood - Steroid Sensitive - No Histology Congenital Nephrotic Syndrome (Cns) - No Histology Congenital Nephrotic Syndrome (Cns) - Finnish Type - No Histology Congenital Nephrotic Syndrome (Cns) - Finnish Type - Histologically Proven Congenital Nephrotic Syndrome (Cns) - Diffuse Mesangial Sclerosis Congenital Nephrotic Syndrome (Cns) - Focal Segmental Glomerulosclerosis (Fsgs) Denys-Drash Syndrome Congenital Nephrotic Syndrome (Cns) - Congenital Infection Minimal Change Nephropathy - No Histology Minimal Change Nephropathy - Histologically Proven Iga Nephropathy - No Histology Iga Nephropathy - Histologically Proven Familial Iga Nephropathy - No Histology Familial Iga Nephropathy - Histologically Proven Iga Nephropathy Secondary To Liver Cirrhosis - No Histology Iga Nephropathy Secondary To Liver Cirrhosis - Histologically Proven Igm - Associated Nephropathy Membranous Nephropathy - Idiopathic Membranous Nephropathy - Malignancy Associated Membranous Nephropathy - Drug Induced Membranous Nephropathy - Infection Associated Mesangiocapillary Glomerulonephritis Type 1 Mesangiocapillary Glomerulonephritis Type 2 (Dense Deposit Disease) Mesangiocapillary Glomerulonephritis Type 3 Idiopathic Rapidly Progressive (Crescentic) Glomerulonephritis Primary Focal Segmental Glomerulosclerosis (Fsgs) Familial Focal Segmental Glomerulosclerosis (Fsgs) - Autosomal Recessive - No Histology Familial Focal Segmental Glomerulosclerosis (Fsgs) - Autosomal Recessive - Histologically Proven Familial Focal Segmental Glomerulosclerosis (Fsgs) - Autosomal Dominant - No Histology Familial Focal Segmental Glomerulosclerosis (Fsgs) - Autosomal Dominant - Histologically Proven Focal Segmental Glomerulosclerosis (Fsgs) Secondary To Obesity - No Histology Focal Segmental Glomerulosclerosis (Fsgs) Secondary To Obesity - Histologically Proven Diffuse Endocapillary Glomerulonephritis Mesangial Proliferative Glomerulonephritis Focal And Segmental Proliferative Glomerulonephritis Glomerulonephritis - Secondary To Other Systemic Disease Glomerulonephritis - Histologically Indeterminate Systemic Vasculitis - Anca Negative - Histologically Proven Systemic Vasculitis - Anca Positive - No Histology Granulomatosis With Polyangiitis - No Histology Granulomatosis With Polyangiitis - Histologically Proven Microscopic Polyangiitis - Histologically Proven Churg-Strauss Syndrome - No Histology Churg-Strauss Syndrome - Histologically Proven Polyarteritis Nodosa Anti-Glomerular Basement Membrane (Gbm) Disease / Goodpasture'S Syndrome - No Histology Anti-Glomerular Basement Membrane (Gbm) Disease / Goodpasture'S Syndrome - Histologically Proven Systemic Lupus Erythematosus / Nephritis - No Histology Systemic Lupus Erythematosus / Nephritis - Histologically Proven Henoch-Schonlein Purpura / Nephritis - No Histology Henoch-Schonlein Purpura / Nephritis - Histologically Proven Renal Scleroderma / Systemic Sclerosis - No Histology Renal Scleroderma / Systemic Sclerosis - Histologically Proven Essential Mixed Cryoglobulinaemia - No Histology Essential Mixed Cryoglobulinaemia - Histologically Proven Cryoglobulinaemia Secondary To Hepatitis C - No Histology Cryoglobulinaemia Secondary To Hepatitis C - Histologically Proven Cryoglobulinaemia Secondary To Systemic Disease - No Histology Cryoglobulinaemia Secondary To Systemic Disease - Histologically Proven Primary Reflux Nephropathy - Sporadic Familial Reflux Nephropathy Congenital Dysplasia / Hypoplasia Multicystic Dysplastic Kidneys Dysplasia Due To Fetal Ace-Inhibitor Exposure Glomerulocystic Disease Congenital Pelvi-Ureteric Junction Obstruction Congenital Vesico-Ureteric Junction Obstruction Posterior Urethral Valves Syndrome Of Agenesis Of Abdominal Muscles - Prune Belly Syndrome Congenital Neurogenic Bladder Bladder Exstrophy Megacystis-Megaureter Oligomeganephronia Renal Papillary Necrosis - Cause Unknown Acquired Obstructive Uropathy / Nephropathy Acquired Obstructive Nephropathy Due To Neurogenic Bladder Obstructive Nephropathy Due To Prostatic Hypertrophy Obstructive Nephropathy Due To Prostate Cancer Obstructive Nephropathy Due To Bladder Cancer Obstructive Nephropathy Due To Other Malignancies Idiopathic Retroperitoneal Fibrosis Retroperitoneal Fibrosis Secondary To Malignancies Calculus Nephropathy / Urolithiasis Calcium Oxalate Urolithiasis Enteric Hyperoxaluria Magnesium Ammonium Phosphate (Struvite) Urolithiasis Uric Acid Urolithiasis Tubulointerstitial Nephritis - No Histology Tubulointerstitial Nephritis - Histologically Proven Familial Interstitial Nephropathy - No Histology Familial Interstitial Nephropathy - Histologically Proven Tubulointerstitial Nephritis Associated With Autoimmune Disease - No Histology Tubulointerstitial Nephritis Associated With Autoimmune Disease - Histologically Proven Tubulointerstitial Nephritis With Uveitis (Tinu) - No Histology Tubulointerstitial Nephritis With Uveitis (Tinu) - Histologically Proven Renal Sarcoidosis - No Histology Renal Sarcoidosis - Histologically Proven Aristolochic Acid Nephropathy (Balkan / Chinese Herb / Endemic Nephropathy) - No Histology Aristolochic Acid Nephropathy (Balkan / Chinese Herb / Endemic Nephropathy) - Histologically Proven Drug-Induced Tubulointerstitial Nephritis - No Histology Drug-Induced Tubulointerstitial Nephritis - Histologically Proven Nephropathy Due To Analgesic Drugs - No Histology Nephropathy Due To Analgesic Drugs - Histologically Proven Nephropathy Due To Ciclosporin - No Histology Nephropathy Due To Ciclosporin - Histologically Proven Nephropathy Due To Tacrolimus - No Histology Nephropathy Due To Tacrolimus - Histologically Proven Nephropathy Due To Aminoglycosides - No Histology Nephropathy Due To Aminoglycosides - Histologically Proven Nephropathy Due To Amphotericin - No Histology Nephropathy Due To Amphotericin - Histologically Proven Nephropathy Due To Cisplatin - No Histology Nephropathy Due To Cisplatin - Histologically Proven Nephropathy Due To Lithium - No Histology Nephropathy Due To Lithium - Histologically Proven Lead Induced Nephropathy - No Histology Lead Induced Nephropathy - Histologically Proven Acute Urate Nephropathy - No Histology Acute Urate Nephropathy - Histologically Proven Chronic Urate Nephropathy - Histologically Proven Radiation Nephritis Renal / Perinephric Abscess Renal Tuberculosis Leptospirosis Hantavirus Nephropathy Xanthogranulomatous Pyelonephritis Nephropathy Related To Hiv - No Histology Nephropathy Related To Hiv - Histologically Proven Schistosomiasis Other Specific Infection Diabetic Nephropathy In Type I Diabetes - No Histology Diabetic Nephropathy In Type I Diabetes - Histologically Proven Diabetic Nephropathy In Type Ii Diabetes - No Histology Diabetic Nephropathy In Type Ii Diabetes - Histologically Proven Chronic Hypertensive Nephropathy - No Histology Chronic Hypertensive Nephropathy - Histologically Proven Malignant Hypertensive Nephropathy / Accelerated Hypertensive Nephropathy - No Histology Malignant Hypertensive Nephropathy / Accelerated Hypertensive Nephropathy - Histologically Proven Ageing Kidney - No Histology Ischaemic Nephropathy - No Histology Ischaemic Nephropathy / Microvascular Disease - Histologically Proven Renal Artery Stenosis Atheroembolic Renal Disease - No Histology Atheroembolic Renal Disease - Histologically Proven Fibromuscular Dysplasia Of Renal Artery Renal Arterial Thrombosis / Occlusion Renal Vein Thrombosis Cardiorenal Syndrome Hepatorenal Syndrome Renal Amyloidosis Aa Amyloid Secondary To Chronic Inflammation Al Amyloid Secondary To Plasma Cell Dyscrasia Familial Amyloid Secondary To Protein Mutations - No Histology Familial Amyloid Secondary To Protein Mutations - Histologically Proven Familial Aa Amyloid Secondary To Familial Mediterranean Fever / Traps (Hibernian Fever) - No Histology Familial Aa Amyloid Secondary To Familial Mediterranean Fever / Traps (Hibernian Fever) - Histologically Proven Myeloma Kidney - No Histology Myeloma Cast Nephropathy - Histologically Proven Light Chain Deposition Disease Immunotactoid / Fibrillary Nephropathy Haemolytic Uraemic Syndrome (Hus) - Diarrhoea Associated Atypical Haemolytic Uraemic Syndrome (Hus) - Diarrhoea Negative Thrombotic Thrombocytopenic Purpura (Ttp) Haemolytic Uraemic Syndrome (Hus) Secondary To Systemic Disease Congenital Haemolytic Uraemic Syndrome (Hus) Familial Haemolytic Uraemic Syndrome (Hus) Familial Thrombotic Thrombocytopenic Purpura (Ttp) Nephropathy Due To Pre-Eclampsia / Eclampsia Sickle Cell Nephropathy - No Histology Sickle Cell Nephropathy - Histologically Proven Autosomal Dominant (Ad) Polycystic Kidney Disease Autosomal Dominant (Ad) Polycystic Kidney Disease Type I Autosomal Dominant (Ad) Polycystic Kidney Disease Type Ii Autosomal Recessive (Ar) Polycystic Kidney Disease Alport Syndrome - No Histology Alport Syndrome - Histologically Proven Benign Familial Haematuria Thin Basement Membrane Disease Cystic Kidney Disease Medullary Cystic Kidney Disease Type I Medullary Cystic Kidney Disease Type Ii Uromodulin-Associated Nephropathy (Familial Juvenile Hyperuricaemic Nephropathy) Nephronophthisis Nephronophthisis - Type 1 (Juvenile Type) Nephronophthisis - Type 2 (Infantile Type) Nephronophthisis - Type 3 (Adolescent Type) Nephronophthisis - Type 4 (Juvenile Type) Nephronophthisis - Type 5 Nephronophthisis - Type 6 Primary Fanconi Syndrome Tubular Disorder As Part Of Inherited Metabolic Diseases Dent Disease Lowe Syndrome (Oculocerebrorenal Syndrome) Inherited Aminoaciduria Cystinuria Cystinosis Inherited Renal Glycosuria Hypophosphataemic Rickets X-Linked (Xl) Hypophosphataemic Rickets Autosomal Recessive (Ar) Primary Renal Tubular Acidosis (Rta) Proximal Renal Tubular Acidosis (Rta) - Type Ii Distal Renal Tubular Acidosis (Rta) - Type I Distal Renal Tubular Acidosis With Sensorineural Deafness - Gene Mutations Nephrogenic Diabetes Insipidus Lesch Nyhan Syndrome - Hypoxanthine Guanine Phosphoribosyl Transferase Deficiency Phosphoribosyl Pyrophosphate Synthetase (Prpps) Superactivity Alagille Syndrome Bartter Syndrome Gitelman Syndrome Liddle Syndrome Apparent Mineralocorticoid Excess Glucocorticoid Suppressible Hyperaldosteronism Inherited / Genetic Diabetes Mellitus Type Ii Pseudohypoaldosteronism Type 1 Pseudohypoaldosteronism Type 2 (Gordon Syndrome) Familial Hypocalciuric Hypercalcaemia Familial Hypercalciuric Hypocalcaemia Familial Hypomagnesaemia Primary Hyperoxaluria Primary Hyperoxaluria Type I Primary Hyperoxaluria Type Ii Fabry Disease - No Histology Fabry Disease - Histologically Proven Xanthinuria Nail-Patella Syndrome Rubinstein-Taybi Syndrome Tuberous Sclerosis Von Hippel-Lindau Disease Medullary Sponge Kidneys Horse-Shoe Kidney Frasier Syndrome Branchio-Oto-Renal Syndrome Williams Syndrome Townes-Brocks Syndrome Lawrence-Moon-Biedl / Bardet-Biedl Syndrome Mitochondrial Cytopathy Familial Nephropathy Acute Kidney Injury Acute Kidney Injury Due To Hypovolaemia Acute Kidney Injury Due To Circulatory Failure Acute Kidney Injury Due To Sepsis Acute Kidney Injury Due To Rhabdomyolysis Acute Kidney Injury Due To Nephrotoxicity Acute Cortical Necrosis Acute Pyelonephritis Kidney Tumour Renal Cell Carcinoma - Histologically Proven Transitional Cell Carcinoma - Histologically Proven Wilms Tumour - Histologically Proven Mesoblastic Nephroma - Histologically Proven Single Kidney Identified In Adulthood Chronic Kidney Disease (Ckd) / Chronic Renal Failure (Crf) Caused By Tumour Nephrectomy Chronic Kidney Disease (Ckd) / Chronic Renal Failure (Crf) Due To Traumatic Loss Of Kidney Chronic Kidney Disease (Ckd) / Chronic Renal Failure (Crf) Due To Donor Nephrectomy Chronic Kidney Disease (Ckd) / Chronic Renal Failure (Crf) - Aetiology Uncertain / Unknown - No Histology Chronic Kidney Disease (Ckd) / Chronic Renal Failure (Crf) - Aetiology Uncertain / Unknown - Histologically Proven Haematuria And Proteinuria - No Histology Nephrotic Syndrome Of Childhood - Steroid Resistant - No Histology Nephrotic Syndrome Of Childhood - No Trial Of Steroids - No Histology Renal Cysts And Diabetes Syndrome Chronic Urate Nephropathy - No Histology Chronic Renal Failure Due To Systemic Infection Renal Coloboma Syndrome Hypercalcaemic Nephropathy Retroperitoneal Fibrosis Secondary To Peri-Aortitis Retroperitoneal Fibrosis Secondary To Drugs Renal Failure Chronic Renal Failure Isolated Haematuria - No Histology Isolated Proteinuria - No Histology Primary Hyperoxaluria Type Iii Glomerulonephritis - No Histology Systemic vasculitis - ANCA negative - no histology Systemic vasculitis - ANCA positive - histologically proven