What cause chronic kidney disease?

Benign prostatic hyperplasia Hereditary onycho-osteodysplasia uracil plasmacytoma carmustine Lomustine Nitrosourea Alström Syndrome type 2 diabetes Bismuth Bardet-Biedl syndrome hydronephrosis diabetes mellitus type 1 Gaucher's disease IgA nephropathy Lesch-Nyhan syndrome Alport syndrome systemic scleroderma renal artery stenosis vesicoureteral reflux barbiturate dependence medullary sponge kidney cystinosis Schistosoma haematobium Autosomal dominant polycystic kidney glomerulosclerosis Denys-Drash syndrome Schulman-Upshaw syndrome reflux nephropathy familial Mediterranean fever Idiopathic multicentric osteolysis X-linked hypophosphataemia Hyperuricemic nephropathy, familial juvenile type 1 Light chain disease primary hyperoxaluria Jeune thoracic dystrophy syndrome Glycogenosis type 1b Xanthogranulomatous pyelonephritis X-linked recessive nephrolithiasis type 1 Dioctophyma renale Carnosine Dimethylglycine Polycystic kidney disease, autosomal recessive Allantoin Hippuric acid Hydroxykynurenine L-Hydroxykynurenine Creatinine 2,8 dihydroxy-adenine urolithiasis Frasier syndrome Balkan endemic nephropathy Galloway Mowat syndrome Senior-Løken syndrome Lecithin cholesterol acyltransferase deficiency Wegener granulomatosis Congenital nephrotic syndrome Townes-Brocks syndrome Glomerulocystic kidney disease Barakat syndrome Sensenbrenner syndrome Essential hypertension papillorenal syndrome Pyelonephritis, chronic Lowe syndrome Hyperoxaluria, primary type 2 Finnish congenital nephrotic syndrome.

Bardet-Biedl syndrome Bardet-Biedl syndrome (an autosomal recessive disorder characterized by retinitis pigmentosa; polydactyly; obesity; mental retardation; hypogenitalism; renal dysplasia; and short stature) hydronephrosis hydronephrosis, distention and dilation of the renal pelvis, usually caused by obstruction of the free flow of urine from the kidney wikipedia diabetes mellitus type 1 Diabetes mellitus type 1, a form of diabetes mellitus wikipedia Gaucher's disease Gaucher's disease, a most common of the lysosomal storage diseases wikipedia IgA nephropathy IgA nephropathy, a form of glomerulonephritis wikipedia Lesch-Nyhan syndrome Lesch-Nyhan syndrome (an X-linked inherited syndrome caused by mutations in the gene that encodes the enzyme hypoxanthine-guanine phosphoribosyltransferase, resulting in accumulation of uric acid in the body) wikipedia Alport syndrome Alport syndrome, a genetic disorder characterized by glomerulonephritis, endstage kidney disease, and hearing loss wikipedia systemic scleroderma Systemic sclerosis or systemic scleroderma, the autoimmune or connective tissue disease wikipedia renal artery stenosis renal artery stenosis, a narrowing of the renal artery, most often caused by atherosclerosis or fibromuscular dysplasia wikipedia vesicoureteral reflux vesicoureteral reflux, an abnormal movement of urine from the bladder into ureters or kidneys wikipedia barbiturate dependence membranous glomerulonephritis, also known as membranous nephropathy, a slowly progressive disease of the kidney affecting mostly patients between ages of 30 and 50 years wikipedia medullary sponge kidney Also known as Cacchi-Ricci disease, Medullary sponge kidney, a congenital disorder of the kidneys characterized by a cystic dilatation of the collecting tubules in one or both kidneys wikipedia cystinosis cystinosis, an autosomal recessive genetic disorder of the renal tubules, characterized by the presence of carbohydrates and amino acids in the urine, excessive urination, and low blood levels of potassium and phosphates wikipedia Schistosoma haematobium Schistosoma haematobium, an important digenetic trematode, and found in the Middle East, India, Portugal and Africa wikipedia Autosomal dominant polycystic kidney Autosomal dominant polycystic kidney disease, the most prevalent, potentially lethal, monogenic human disorder wikipedia glomerulosclerosis glomerulosclerosis, referring to a hardening of the glomerulus in the kidney wikipedia Denys-Drash syndrome Denys-Drash syndrome, a syndrome characterized by the following conditions: * gonadal dysgenesis * nephropathy * Wilms tumor Denys-Drash Syndrome is a very rare disorder wikipedia Schulman-Upshaw syndrome thrombotic thrombocytopenic purpura, a rare disorder of the blood coagulation system wikipedia reflux nephropathy Reflux nephropathy, RN, a term applied when small and scarred kidneys, associated with vesico-ureteric reflux wikipedia familial Mediterranean fever familial Mediterranean fever, a hereditary inflammatory disorder that affects groups of patients originating from around the Mediterranean Sea wikipedia Idiopathic multicentric osteolysis Idiopathic multicentric osteolysis, the cause and medical concept with Mesh code "D010015" and DiseasesDB code "33388" X-linked hypophosphataemia X-linked hypophosphataemia (group of disorders characterized by rickets but not responding to high doses of vitamin D; most are forms of familial hypophosphatemic rickets) Hyperuricemic nephropathy, familial juvenile type 1 Hyperuricemic nephropathy, familial juvenile type 1, the cause and medical condition with DiseasesDB code "33754" Light chain disease Light chain disease (a condition in which plasma cells secrete immunoglobulin light chains of only one type, kappa or lambda) primary hyperoxaluria Hyperoxaluria, primary type 1 (a genetic disorder characterized by excretion of large amounts of oxalates in urine; nephrolithiasis; nephrocalcinosis; early onset of renal failure; and often a generalized deposit of calcium oxalate) wikipedia Jeune thoracic dystrophy syndrome Jeune thoracic dystrophy syndrome (congenital polychondrodystrophy in which narrow and rigid thoracic cage results in asphyxia, ranging in severity from mild cases with minimal respiratory symptoms to fatal asphyxiation) Glycogenosis type 1b Glycogenosis type 1b, the cause and medical concept with DiseasesDB code "32132" Xanthogranulomatous pyelonephritis Xanthogranulomatous pyelonephritis (a chronic inflammatory condition of the kidney resulting in diffuse renal destruction, a grossly enlarged and nonfunctioning kidney associated with nephrolithiasis and kidney stones) X-linked recessive nephrolithiasis type 1 X-linked recessive nephrolithiasis type 1, the cause and medical condition with DiseasesDB code "31323" Dioctophyma renale Dioctophyma renale, the cause and medical concept with Mesh code "D017189" and DiseasesDB code "33912" Carnosine Carnosine, the chemical compound, a cause of the phenomenon chronic renal failure Dimethylglycine Dimethylglycine, the chemical compound, a cause of the phenomenon Barrett's esophagus and coronary artery disease Polycystic kidney disease, autosomal recessive Polycystic kidney disease, autosomal recessive (a genetic disorder with autosomal recessive inheritance, characterized by multiple cysts in both kidneys and associated liver lesions) Allantoin Allantoin, the chemical compound, a cause of the phenomenon multiple sclerosis and Guillain-Barré syndrome Hippuric acid Hippuric acid, the chemical compound, a cause of the phenomenon asthma and lung cancer Hydroxykynurenine Hydroxykynurenine, the chemical compound, a cause of the phenomenon Huntington's disease and chronic renal failure L-Hydroxykynurenine L-Hydroxykynurenine, the chemical compound, a cause of the phenomenon Huntington's disease and chronic renal failure Creatinine Creatinine, the chemical compound, a cause of the phenomenon cystinosis and Isovaleric acidemia 2,8 dihydroxy-adenine urolithiasis Adenine phosphoribosyltransferase deficiency, an autosomal recessive metabolic disorder resulting in accumulation and urinary excretion of the insoluble purine 2,8-dihydroxyadenine wikipedia Frasier syndrome Frasier syndrome, the urogenital anomaly associated with the WT1 gene wikipedia Balkan endemic nephropathy Balkan nephropathy, a form of interstitial nephritis wikipedia Galloway Mowat syndrome Galloway Mowat syndrome, a very rare autosomal recessive genetic disorder, consisting of a variety of features including hiatal hernia, microcephaly and nephrotic syndrome wikipedia Senior-Løken syndrome Senior-Løken syndrome, a congenital eye disorder, first characterized in 1961 wikipedia Lecithin cholesterol acyltransferase deficiency Lecithin cholesterol acyltransferase deficiency (disease characterized by abnormally low levels of plasma lecithin cholesterol acyl transferase; clinical manifestations include corneal opacity, anemia, and proteinuria) wikipedia Wegener granulomatosis Wegener granulomatosis (a multisystemic disease of a complex genetic background) Congenital nephrotic syndrome Congenital nephrotic syndrome, an inherited disorder characterized by protein in the urine and swelling of the body wikipedia Townes-Brocks syndrome Townes-Brocks syndrome, a rare genetic disease that affects fewer than 200 people in the entire world wikipedia Glomerulocystic kidney disease Glomerulocystic kidney disease, the cause and medical concept with DiseasesDB code "30689" Barakat syndrome Barakat syndrome, the rare disease characterized by hypoparathyroidism, sensorineural deafness and renal disease, and hence also known as HDR syndrome wikipedia Sensenbrenner syndrome Sensenbrenner syndrome (defects of ectoderm-derived structures (sparse, slow-growing, fine and hyperpigmented hair, and tooth abnormalities) in association with bone anomalies) Essential hypertension Essential hypertension (hypertension occurring without preexisting renal disease or known organic cause) papillorenal syndrome Papillorenal syndrome, also called Renal-coloboma syndrome, an autosomal dominant genetic disorder marked by underdevelopment of the kidney and colobomas of the optic nerve wikipedia Pyelonephritis, chronic Pyelonephritis, chronic, the Phenomenon and medical condition with DiseasesDB code "11052" Lowe syndrome Lowe syndrome (a syndrome of congenital cataracts, hydrophthalmia, delayed growth and mental development, vitamin D-resistant rickets, aminoaciduria, and reduced production of ammonia by the kidneys) Hyperoxaluria, primary type 2 Hyperoxaluria, primary type 2, the cause and medical concept with DiseasesDB code "29828" Finnish congenital nephrotic syndrome Finnish congenital nephrotic syndrome, the cause and medical concept with DiseasesDB code "29909.

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