| Disease | Prevalence Estimate | US people estimate | Statistic Used for Calculation |
| Kidney damage -- 1,2-Dichloromethane |
N/A |
N/A |
No information
|
| Kidney damage -- Acetaminophen |
N/A |
N/A |
No information
|
| Kidney damage -- Aminoglycosides |
N/A |
N/A |
No information
|
| Kidney damage -- Aminosalicylic Acid |
N/A |
N/A |
No information
|
| Kidney damage -- Amphotericin B |
N/A |
N/A |
No information
|
| Kidney damage -- Amyl Alcohol |
N/A |
N/A |
No information
|
| Kidney damage -- analgesics |
N/A |
N/A |
No information
|
| Kidney damage -- Anti-cancer drugs |
N/A |
N/A |
No information
|
| Kidney damage -- antibiotics |
N/A |
N/A |
No information
|
| Kidney damage -- Aristolochic acid |
N/A |
N/A |
No information
|
| Kidney damage -- Arsenic |
N/A |
N/A |
No information
|
| Kidney damage -- Aspirin |
N/A |
N/A |
No information
|
| Kidney damage -- Automobile exhaust |
N/A |
N/A |
No information
|
| Kidney damage -- Bacitracin |
N/A |
N/A |
No information
|
| Kidney damage -- Bismuth |
N/A |
N/A |
No information
|
| Kidney damage -- Cadmium |
N/A |
N/A |
No information
|
| Kidney damage -- Carbon Tetrachloride |
N/A |
N/A |
No information
|
| Kidney damage -- Cephaloridine |
N/A |
N/A |
No information
|
| Kidney damage -- Chloroform |
N/A |
N/A |
No information
|
| Kidney damage -- Chromium |
N/A |
N/A |
No information
|
| Kidney damage -- Cisplatin |
N/A |
N/A |
No information
|
| Kidney damage -- Contrast agents |
N/A |
N/A |
No information
|
| Kidney damage -- Copper |
N/A |
N/A |
No information
|
| Kidney damage -- Cyclophosphamide |
N/A |
N/A |
No information
|
| Kidney damage -- Cyclosporin |
N/A |
N/A |
No information
|
| Kidney damage -- Degreasing solvents |
N/A |
N/A |
No information
|
| Kidney damage -- Dichloroacetylene |
N/A |
N/A |
No information
|
| Kidney damage -- Diethylene glycol |
N/A |
N/A |
No information
|
| Kidney damage -- Dioxane |
N/A |
N/A |
No information
|
| Kidney damage -- Ethylene Glycol |
N/A |
N/A |
No information
|
| Kidney damage -- Ethylene glycol ethers |
N/A |
N/A |
No information
|
| Kidney damage -- Fuels |
N/A |
N/A |
No information
|
| Kidney damage -- Gasoline |
N/A |
N/A |
No information
|
| Kidney damage -- Germanium |
N/A |
N/A |
No information
|
| Kidney damage -- Glue solvent vapors |
N/A |
N/A |
No information
|
| Kidney damage -- Glues |
N/A |
N/A |
No information
|
| Kidney damage -- Gold |
N/A |
N/A |
No information
|
| Kidney damage -- Hairdressing solvents |
N/A |
N/A |
No information
|
| Kidney damage -- Hairdressing sprays |
N/A |
N/A |
No information
|
| Kidney damage -- Heavy metals |
N/A |
N/A |
No information
|
| Kidney damage -- Herbicide |
N/A |
N/A |
No information
|
| Kidney damage -- Hexachloro-1,3-butadiene |
N/A |
N/A |
No information
|
| Kidney damage -- Hydrocarbons |
N/A |
N/A |
No information
|
| Kidney damage -- Ibuprofen |
N/A |
N/A |
No information
|
| Kidney damage -- Lead |
N/A |
N/A |
No information
|
| Kidney damage -- Lithium |
N/A |
N/A |
No information
|
| Kidney damage -- Mercury |
N/A |
N/A |
No information
|
| Kidney damage -- Methanol |
N/A |
N/A |
No information
|
| Kidney damage -- Methemoglobin-producing agents |
N/A |
N/A |
No information
|
| Kidney damage -- Methicillin |
N/A |
N/A |
No information
|
| Kidney damage -- Neomycin |
N/A |
N/A |
No information
|
| Kidney damage -- Nonsteroidal anti-inflammatory drugs |
N/A |
N/A |
No information
|
| Kidney damage -- Oxytetracycline |
N/A |
N/A |
No information
|
| Kidney damage -- Paint thinners |
N/A |
N/A |
No information
|
| Kidney damage -- Paints |
N/A |
N/A |
No information
|
| Kidney damage -- Paraquat ochratoxin A |
N/A |
N/A |
No information
|
| Kidney damage -- Perchloroethylene |
N/A |
N/A |
No information
|
| Kidney damage -- Pesticide solvents |
N/A |
N/A |
No information
|
| Kidney damage -- Pesticides |
N/A |
N/A |
No information
|
| Kidney damage -- Platinum |
N/A |
N/A |
No information
|
| Kidney damage -- Polymyxin |
N/A |
N/A |
No information
|
| Kidney damage -- Prostaglandin synthetase inhibitors |
N/A |
N/A |
No information
|
| Kidney damage -- Rifampin |
N/A |
N/A |
No information
|
| Kidney damage -- Silica |
N/A |
N/A |
No information
|
| Kidney damage -- Silicon compounds |
N/A |
N/A |
No information
|
| Kidney damage -- Silver |
N/A |
N/A |
No information
|
| Kidney damage -- Styrene |
N/A |
N/A |
No information
|
| Kidney damage -- Sulphonamides |
N/A |
N/A |
No information
|
| Kidney damage -- Thallium |
N/A |
N/A |
No information
|
| Kidney damage -- Toluene |
N/A |
N/A |
No information
|
| Kidney damage -- Trichloroethane |
N/A |
N/A |
No information
|
| Kidney damage -- Trichloroethylene |
N/A |
N/A |
No information
|
| Kidney damage -- Trimethropin |
N/A |
N/A |
No information
|
| Kidney damage -- Uranium |
N/A |
N/A |
No information
|
| Kidney damage due to chemicals |
N/A |
N/A |
No information
|
| Kidney Cancer |
N/A |
N/A |
No information
|
| Renal cancer |
N/A |
N/A |
No information
|
| Urethral cancer |
N/A |
N/A |
No information
|
| Urachal cancer |
N/A |
N/A |
No information
|
| Cardiomyopathy -- renal anomalies |
N/A |
N/A |
No information
|
| Renal cancer, familial |
N/A |
N/A |
No information
|
| Diabetic Nephropathy |
N/A |
N/A |
No information
|
| Kidney conditions |
approx 1 in 66 or 1.50% or 4.1 million people in USA |
4,080,000 |
15 per 1000 (NHIS95: "kidney trouble")
|
| Kidney disease |
approx 1 in 36 or 2.72% or 7.4 million people in USA |
7,399,999 |
7.4 million adults in the USA 1988-94 (American Journal of Kidney Disease)
|
| Proximal tubulopathy -- diabetes mellitus -- cerebellar ataxia |
N/A |
N/A |
No information
|
| Bladder conditions |
N/A |
N/A |
No information
|
| Bladder Incontinence (Pregnancy) |
approx 1 in 203 or 0.49% or 1.3 million people in USA |
1,333,333 |
1-in-3 pregnant women approximately
|
| Urinary incontinence in children |
N/A |
N/A |
No information
|
| Cystitis |
approx 1 in 43 or 2.28% or 6.2 million people in USA |
6,200,000 |
6.2 million adults self-reported having a bladder infection for more than 3 months in the US 1988-1994 (Weighted Analysis of 1988-1994, NHANES, NIDDK)
|
| Interstitial cystitis |
approx 1 in 321 or 0.31% or 847,000 people in USA |
846,999 |
847,000 in the USA 1988-1994 (Weighted Analysis of 1988-1994 National Health and Nutrition Survey, 2003)
|
| Urinary tract infections |
N/A |
N/A |
No information
|
| Urinary tract infections (child) |
approx 1 in 33 or 3.00% or 8.2 million people in USA |
8,160,000 |
3% of girls and 1% of boys before age 11
|
| Urinary stones |
approx 1 in 19 or 5.20% or 14.1 million people in USA |
14,143,999 |
5.2% of adults in the USA 1988-1994 (Weighted Analysis of 1988-1994 National Health and Nutrition Survey, 2003)
|
| Vesicoureteral reflux |
N/A |
N/A |
No information
|
| Neurogenic bladder |
N/A |
N/A |
No information
|
| Incontinence |
N/A |
N/A |
No information
|
| Urine retention |
N/A |
N/A |
No information
|
| Acute urinary conditions |
N/A |
N/A |
No information
|
| Acute urinary retention |
N/A |
N/A |
No information
|
| Proteinuria |
N/A |
N/A |
No information
|
| Bedwetting |
N/A |
N/A |
No information
|
| Nephritis |
N/A |
N/A |
No information
|
| Pyelonephritis |
N/A |
N/A |
No information
|
| Urethritis |
N/A |
N/A |
No information
|
| Urinary Incontinence |
approx 1 in 20 or 4.78% or 13 million people in USA |
13,000,000 |
13 million adults (NIDDK); 1 in 10 over 65 (NWHIC).
|
| Stress incontinence |
N/A |
N/A |
No information
|
| Urge incontinence |
N/A |
N/A |
No information
|
| Overflow incontinence |
N/A |
N/A |
No information
|
| Nocturnal enuresis |
N/A |
N/A |
No information
|
| Urinary disorders |
N/A |
N/A |
No information
|
| Anuria |
N/A |
N/A |
No information
|
| Urethral stricture |
N/A |
N/A |
No information
|
| Urethral syndrome |
N/A |
N/A |
No information
|
| Nephrocalcinosis |
N/A |
N/A |
No information
|
| Simple kidney cysts |
N/A |
N/A |
No information
|
| Polycystic kidney disease |
approx 1 in 453 or 0.22% or 600,000 people in USA |
600,000 |
600,000 Americans
|
| Acquired Cystic Kidney Disease |
N/A |
N/A |
No information
|
| Autosomal dominant polycystic kidney disease |
approx 1 in 503 or 0.20% or 540,000 people in USA |
539,999 |
540,000 Americans approximately (90% of PKD)
|
| Autosomal Recessive Polycystic Kidney Disease |
approx 1 in 20,000 or 0.00% or 13,600 people in USA |
13,599 |
estimated 1 per 20,000 - 40,000 people suffer from the autosomal recessive type of polycystic kidney disease, Genetics Home Reference website
|
| Diabetes Insipidus |
N/A |
N/A |
No information
|
| Kidney Dialysis |
approx 1 in 946 or 0.11% or 287,493 people in USA |
287,493 |
287,494 people in the USA 2001 (United States Renal Data System 2003 Annual Data Report, 2003)
|
| Urinary system cancer |
N/A |
N/A |
No information
|
| Bladder Cancer |
N/A |
N/A |
bladder cancer is the fourth most common type of cancer in men in the US, Genetics Home Reference website
|
| Bladder papilloma |
N/A |
N/A |
No information
|
| Ureter cancer |
N/A |
N/A |
No information
|
| Wilms' tumor |
N/A |
N/A |
No information
|
| Systemic Lupus Erythematosus with Nephritis, Susceptibility to, 1 |
N/A |
N/A |
No information
|
| Hemolytic Uremic Syndrome, Atypical, Susceptibility to, 6 |
N/A |
N/A |
No information
|
| Hemolytic Uremic Syndrome, Atypical, Susceptibility to, 5 |
N/A |
N/A |
No information
|
| Hemolytic Uremic Syndrome, Atypical, Susceptibility to, 4 |
N/A |
N/A |
No information
|
| Hemolytic Uremic Syndrome, Atypical, Susceptibility to, 3 |
N/A |
N/A |
No information
|
| Hemolytic Uremic Syndrome, Atypical, Susceptibility to, 2 |
N/A |
N/A |
No information
|
| Hemolytic Uremic Syndrome, Atypical, Susceptibility to, 1 |
N/A |
N/A |
No information
|
| Nephritis, Familial, without Deafness or Ocular Defect |
N/A |
N/A |
No information
|
| Adult-onset Renal Failure |
N/A |
N/A |
No information
|
| Nephropathy, Familial |
N/A |
N/A |
No information
|
| Renal Failure, Progressive, with Hypertension |
N/A |
N/A |
No information
|
| Progressive nephropathy with hypertension, autosomal dominant |
N/A |
N/A |
No information
|
| Decreased urine chloride |
N/A |
N/A |
No information
|
| Decreased urine output |
N/A |
N/A |
No information
|
| Decreased urine stream |
N/A |
N/A |
No information
|
| Decreased urine specific gravity |
N/A |
N/A |
No information
|
| Hypercalcuria |
N/A |
N/A |
No information
|
| Kidney disease-Induced Hypertension |
N/A |
N/A |
No information
|
| Chronic pyelonephritis |
N/A |
N/A |
No information
|
| Primary Glomerulonephritis |
approx 1 in 4,428 or 0.02% or 61,422 people in USA |
61,422 |
61,423 people with Primary Glomerulonephritis in the USA 1996 1
|
| Glomerulonephritis |
N/A |
N/A |
No information
|
| Kidney stones |
N/A |
N/A |
No information
|
| Glomerular Disease |
N/A |
N/A |
No information
|
| Glomerulosclerosis |
N/A |
N/A |
No information
|
| Lupus nephritis |
N/A |
N/A |
No information
|
| End-stage renal disease |
approx 1 in 693 or 0.14% or 392,022 people in USA |
392,022 |
392,023 people in the USA 2001 (United States Renal Data System 2003 Annual Data Report, 2003)
|
| IgA nephropathy |
approx 1 in 4,428 or 0.02% or 61,422 people in USA |
61,422 |
61,423 people in the USA 1996 1
|
| Nephrotic syndrome |
N/A |
N/A |
No information
|
| Childhood nephrotic syndrome |
N/A |
N/A |
No information
|
| Renal Tubular Acidosis |
N/A |
N/A |
No information
|
| Proximal Renal Tubular Acidosis |
N/A |
N/A |
No information
|
| Renal carbuncle |
N/A |
N/A |
No information
|
| Renal osteodystrophy |
N/A |
N/A |
No information
|
| Renal tuberculosis |
N/A |
N/A |
No information
|
| Nephropathy |
N/A |
N/A |
No information
|
| Chronic renal insufficiency |
N/A |
N/A |
No information
|
| Classic Distal Renal Tubular Acidosis |
N/A |
N/A |
No information
|
| Hyperkalemic Renal Tubular Acidosis |
N/A |
N/A |
No information
|
| Cystine stone |
N/A |
N/A |
No information
|
| Kidney transplant |
N/A |
N/A |
No information
|
| Hemodialysis |
N/A |
N/A |
No information
|
| Interstitial nephritis |
N/A |
N/A |
No information
|
| Obstructive nephropathy |
N/A |
N/A |
No information
|
| Reflux nephropathy |
N/A |
N/A |
No information
|
| Continuous incontinence |
N/A |
N/A |
No information
|
| Acute (or transient) urinary incontinence |
N/A |
N/A |
No information
|
| Post streptococcal glomerulonephritis |
N/A |
N/A |
No information
|
| Mesangial proliferative glomerulonephritis |
N/A |
N/A |
No information
|
| Autoimmune Interstitial Cystitis |
N/A |
N/A |
No information
|
| Autoimmune Diabetes Insipidus |
N/A |
N/A |
No information
|
| Gonorrhea |
N/A |
N/A |
No information
|
| Medullary Sponge Kidney |
N/A |
N/A |
No information
|
| Chronic Kidney Disease |
N/A |
N/A |
No information
|
| Overactive bladder/urinary incontinence |
N/A |
N/A |
No information
|
| Alkaptonuria |
approx 1 in 19,000 or 0.01% or 14,315 people in USA |
14,315 |
1 per 19,000 people suffer from alkaptonuria in parts of Slovakia, Genetics Home Reference website
|
| The Primary Hyperoxalurias |
N/A |
N/A |
No information
|
| Trimethylaminuria |
N/A |
N/A |
No information
|
| Aspartylglucosaminuria |
N/A |
N/A |
No information
|
| Cystinuria |
approx 1 in 10,000 or 0.01% or 27,200 people in USA |
27,199 |
approximately 1 per 10,000 people are affected by cystinuria, Genetics Home Reference website
|
| Dicarboxylicaminoaciduria |
N/A |
N/A |
No information
|
| Nephrotic syndrome-like albuminuria |
N/A |
N/A |
No information
|
| Sudden compelling urge to urinate similar to that of benign prostatic hyperplasia |
N/A |
N/A |
No information
|
| Oliguria as in case of renal failure |
N/A |
N/A |
No information
|
| Renal failure-like electrolyte imbalances |
N/A |
N/A |
No information
|
| Urinary outflow obstruction |
N/A |
N/A |
No information
|
| Glomerulonephritis-like microscopic hematuria |
N/A |
N/A |
No information
|
| Uremic encephalopathy |
N/A |
N/A |
No information
|
| AIDS-Associated Nephropathy |
N/A |
N/A |
No information
|
| Maple syrup urine disease, type 1B |
N/A |
N/A |
No information
|
| Eosinophilic cystitis |
N/A |
N/A |
No information
|
| Hematuria |
N/A |
N/A |
No information
|
| Chronic interstitial cystitis |
N/A |
N/A |
No information
|
| Glutaricaciduria type 1 |
N/A |
N/A |
No information
|
| Glutaric aciduria 1 |
N/A |
N/A |
No information
|
| Uremic pericarditis |
N/A |
N/A |
No information
|
| Bartter Syndrome type 4 |
N/A |
N/A |
No information
|
| Bartter Syndrome type 4A |
N/A |
N/A |
No information
|
| Bartter Syndrome type 4B |
N/A |
N/A |
No information
|
| Bartter Syndrome |
N/A |
N/A |
No information
|
| Bartter's syndrome, antenatal type 1 |
N/A |
N/A |
No information
|
| Bartters syndrome, antenatal , type 2 |
N/A |
N/A |
No information
|
| Bartter's syndrome, type 3 |
N/A |
N/A |
No information
|
| Familial Wilms tumor 2 |
N/A |
N/A |
No information
|
| Diabetes Insipidus, Neurogenic |
N/A |
N/A |
No information
|
| Hypospadias 1, X-linked |
N/A |
N/A |
No information
|
| Hypospadias 2, X-linked |
N/A |
N/A |
No information
|
| Hypospadias 3, Autosomal |
N/A |
N/A |
No information
|
| Hypospadias |
N/A |
N/A |
No information
|
| Epispadias |
N/A |
N/A |
No information
|
| Hydronephrosis |
N/A |
N/A |
No information
|
| Nocturia |
N/A |
N/A |
No information
|
| Hypertelorism with esophageal abnormality and hypospadias |
N/A |
N/A |
No information
|
| Spina bifida -- hypospadias |
N/A |
N/A |
No information
|
| Myopathy -- growth and mental retardation -- hypospadias |
N/A |
N/A |
No information
|
| Preaxial deficiency, postaxial polydactyly and hypospadias |
N/A |
N/A |
No information
|
| Tracheoesophageal fistula -- hypospadias |
N/A |
N/A |
No information
|
| Hypospadias familial |
N/A |
N/A |
No information
|
| Preaxial deficiency postaxial polydactyly hypospadias |
N/A |
N/A |
No information
|
| Hypertelorism -- esophageal abnormalities -- hypospadias |
N/A |
N/A |
No information
|
| Hypospadias -- hypertelorism |
N/A |
N/A |
No information
|
| Cataract -- intellectual deficit -- anal atresia -- urinary defects |
N/A |
N/A |
No information
|
| Myopathy -- growth delay -- mental retardation -- hypospadias |
N/A |
N/A |
No information
|
| Ichthyosis mental retardation dwarfism renal impairment |
N/A |
N/A |
No information
|
| Hypotelorism -- cleft palate -- hypospadias |
N/A |
N/A |
No information
|
| Deafness -- hypospadias -- metacarpal and metatarsal synostosis |
N/A |
N/A |
No information
|
| Deafness -- nephritis -- anorectal malformation |
N/A |
N/A |
No information
|
| Overactive Bladder |
N/A |
N/A |
No information
|
| Bladder distention |
N/A |
N/A |
No information
|
| Grasbeck-Imerslund Disease |
N/A |
N/A |
No information
|
| Cobalamin malabsorption, selective, with proteinuria |
N/A |
N/A |
No information
|
| Renovascular stenosis |
N/A |
N/A |
No information
|
| Renal infarction |
N/A |
N/A |
No information
|
| Albuminuria |
N/A |
N/A |
No information
|
| Nonspecific genitourinary infections |
N/A |
N/A |
No information
|
| Uremic frost |
N/A |
N/A |
No information
|
| Renal-hepatic-pancreatic dysplasia -- Dandy Walker cyst |
N/A |
N/A |
No information
|
| Leiomyomatosis of esophagus, cataract and hematuria |
N/A |
N/A |
No information
|
| Horseshoe kidney |
N/A |
N/A |
No information
|
| Wilms tumor 3 |
N/A |
N/A |
No information
|
| Galloway-Mowat Syndrome |
N/A |
N/A |
No information
|
| Galloway syndrome |
N/A |
N/A |
No information
|
| Nephrosis neuronal dysmigration Syndrome |
N/A |
N/A |
No information
|
| Wilms tumor -- aniridia -- genitourinary anomalies -- mental retardation |
N/A |
N/A |
No information
|
| WAGR Syndrome |
N/A |
N/A |
No information
|
| Branchio-oto-renal (BOR) syndrome, type 2 |
N/A |
N/A |
No information
|
| Branchio-Oto-Renal Syndrome |
N/A |
N/A |
No information
|
| Branchio-otoureteral syndrome |
N/A |
N/A |
No information
|
| Bacteriuria |
N/A |
N/A |
No information
|
| Cataract, juvenile, with microcornea and glucosuria |
N/A |
N/A |
No information
|
| Homocystinuria |
approx 1 in 200,000 or 0.00% or 1,360 people in USA |
1,360 |
at least 1 per 200,000 - 335,000 people are affected by homocystinuria worldwide, Genetics Home Reference website
|
| Homocystinuria syndrome |
N/A |
N/A |
No information
|
| Homocystinuria due to defect in methylation (cbl g) |
N/A |
N/A |
No information
|
| Homocystinuria due to defect in methylation cbl e |
N/A |
N/A |
No information
|
| Homocystinuria due to cystathionine beta-synthase deficiency |
N/A |
N/A |
No information
|
| Diabetes insipidus, nephrogenic, recessive type |
N/A |
N/A |
No information
|
| Analgesic nephropathy syndrome |
N/A |
N/A |
No information
|
| Wilms tumour and radial bilateral aplasia |
N/A |
N/A |
No information
|
| Amyloidosis, familial visceral |
N/A |
N/A |
No information
|
| Oliguria |
N/A |
N/A |
No information
|
| Beeturia |
N/A |
N/A |
No information
|
| Bladder diverticulum |
N/A |
N/A |
No information
|
| Osteopetrosis -- renal tubular acidosis |
N/A |
N/A |
No information
|
| Osteopetrosis with renal tubular acidosis |
N/A |
N/A |
No information
|
| Vasopressin-resistant diabetes insipidus |
N/A |
N/A |
No information
|
| Nephrogenic diabetes insipidus |
N/A |
N/A |
No information
|
| Diabetes insipidus primary central |
N/A |
N/A |
No information
|
| Diabetes insipidus, nephrogenic, dominant type |
N/A |
N/A |
No information
|
| Diabetes insipidus, nephrogenic type 2 |
N/A |
N/A |
No information
|
| Diabetes insipidus, diabetes mellitus, optic atrophy |
N/A |
N/A |
No information
|
| Diabetes insipidus, diabetes mellitus, optic atrophy, deafness, mitochondrial form |
N/A |
N/A |
No information
|
| Corpus callosum agenesis double urinary collecting system and trigonocephaly |
N/A |
N/A |
No information
|
| Corpus callosum agenesis double urinary collecting |
N/A |
N/A |
No information
|
| Nephrotic syndrome, idiopathic, steroid-resistant |
N/A |
N/A |
No information
|
| Atherosclerosis- deafness -- diabetes -- epilepsy -- nephropathy |
N/A |
N/A |
No information
|
| Atherosclerosis, premature -- deafness -- diabetes mellitus -- photomyoclonus -- nephropathy -- degenerative neurologic disease |
N/A |
N/A |
No information
|
| Spastic paraplegia nephritis deafness |
N/A |
N/A |
No information
|
| Diabetes, neonatal -- congenital hypothyroidism -- congenital glaucoma -- hepatic fibrosis -- polycystic kidneys |
N/A |
N/A |
No information
|
| Renal tubulopathy -- diabetes mellitus -- cerebellar ataxia |
N/A |
N/A |
No information
|
| Nephrosis, idiopathic, sporadic |
N/A |
N/A |
No information
|
| Serratia urinary tract infection |
N/A |
N/A |
No information
|
| Leukonychia totalis -- trichilemmal cysts -- cilliary dystrophy |
N/A |
N/A |
No information
|
| Arthrogryposis -- renal dysfunction -- cholestasis syndrome |
N/A |
N/A |
No information
|
| Congenital giant megaureter |
N/A |
N/A |
No information
|
| Renal Magnesium Wasting -- hypercalciuria -- nephrocalcinosis -- Ocular disorders |
N/A |
N/A |
No information
|
| Renal hypomagnesemia -- hypercalciuria -- nephrocalcinosis |
N/A |
N/A |
No information
|
| Ischio-spinal dysostosis with cystic kidney disease |
N/A |
N/A |
No information
|
| Ischio-spinal dysostosis -- rib gaps -- nephroblastomatosis |
N/A |
N/A |
No information
|
| Renal abscess |
N/A |
N/A |
No information
|
| Selective Vitamin B12 malabsorption with Proteinuria |
N/A |
N/A |
No information
|
| Renal cell carcinoma, papillary, familial |
N/A |
N/A |
No information
|
| Renal cell carcinoma, papillary, hereditary |
N/A |
N/A |
No information
|
| Renal cell carcinoma, papillary, sporadic |
N/A |
N/A |
No information
|
| Non-Specific Urethritis |
N/A |
N/A |
No information
|
| Perineal hemangioma -- external genitalia malformations -- lipomyelomeningocele -- vesicorenal abnormalities -- imperforate anus |
N/A |
N/A |
No information
|
| Wilms tumor 2 |
N/A |
N/A |
No information
|
| Renal tubular transport disorders, inborn |
N/A |
N/A |
No information
|
| Renal tubular acidosis, distal |
N/A |
N/A |
No information
|
| Renal tubular acidosis progressive nerve deafness |
N/A |
N/A |
No information
|
| Renal tubular acidosis, distal -- type III |
N/A |
N/A |
No information
|
| Renal tubular acidosis, distal -- type I |
N/A |
N/A |
No information
|
| Renal tubular acidosis, distal, type 4 |
N/A |
N/A |
No information
|
| Renal tubular acidosis, distal, autosomal recessive |
N/A |
N/A |
No information
|
| Neuroaxonal dystrophy -- renal tubular acidosis |
N/A |
N/A |
No information
|
| Renal tubular acidosis, distal, autosomal dominant |
N/A |
N/A |
No information
|
| Histidinuria, renal tubular defect |
N/A |
N/A |
No information
|
| Cholestatic jaundice -renal tubular insufficiency |
N/A |
N/A |
No information
|
| Wilms tumor and radial bilateral aplasia |
N/A |
N/A |
No information
|
| Medullary cystic kidney disease, dominant |
N/A |
N/A |
No information
|
| Medullary cystic kidney disease |
N/A |
N/A |
No information
|
| Nephronophthisis, autosomal dominant |
N/A |
N/A |
No information
|
| Nephronophthisis 7 |
N/A |
N/A |
No information
|
| Nephronophthisis 4 |
N/A |
N/A |
No information
|
| Nephronophthisis 3 |
N/A |
N/A |
No information
|
| Nephronophthisis 2 |
N/A |
N/A |
No information
|
| Nephronophthisis -- hepatic fibrosis |
N/A |
N/A |
No information
|
| Juvenile nephronophthisis |
N/A |
N/A |
No information
|
| Nephronophthisis familial, adult -- spastic quadriparesis |
N/A |
N/A |
No information
|
| Benign familial hematuria |
N/A |
N/A |
No information
|
| Polycystic ovaries urethral sphincter dysfunction |
N/A |
N/A |
No information
|
| Polycystic kidney disease, type 2 |
N/A |
N/A |
No information
|
| Polycystic kidneys, severe infantile, with tuberous sclerosis |
N/A |
N/A |
No information
|
| Serpentine fibula -- polycystic kidney syndrome |
N/A |
N/A |
No information
|
| Polycystic kidney disease, adult type |
N/A |
N/A |
No information
|
| Polycystic kidney disease, infantile type |
N/A |
N/A |
No information
|
| Polycystic kidney disease type 1 |
approx 1 in 20,000 or 0.00% or 13,600 people in USA |
13,599 |
estimated 1 per 20,000 - 40,000 people are affected by autosomal dominant polycystic kidney disease, Genetics Home Reference website
|
| Maple syrup urine disease, type II |
N/A |
N/A |
No information
|
| Maple syrup urine disease, type 2 |
N/A |
N/A |
No information
|
| Maple syrup urine disease, type 3 |
N/A |
N/A |
No information
|
| Maple syrup urine disease, type III |
N/A |
N/A |
No information
|
| Maple syrup urine disease |
approx 1 in 384 or 0.26% or 706,493 people in USA |
706,493 |
estimated 1 per 385 infants suffer from maple syrup urine disease in the Old Order Mennonite population, Genetics Home Reference website
|
| Maple syrup urine disease, type 1A |
N/A |
N/A |
No information
|
| MGA 4 |
N/A |
N/A |
No information
|
| $2-methylglutaconic aciduria type 3$ |
approx 1 in 10,000 or 0.01% or 27,200 people in USA |
27,199 |
1 per 10,000 newborns from Iraqi Jewish populations suffer from 2-methylglutaconic aciduria type 3, Genetics Home Reference website
|
| $3-methylglutaconic aciduria, type 4$ |
N/A |
N/A |
No information
|
| $3-methylglutaconic aciduria, type 1$ |
approx 1 in 13,600,000 or 0.00% or 20 people in USA |
20 |
less than 20 cases of 2-methylglutaconic aciduria type 1 have been reported, Genetics Home Reference website
|
| $3 alpha methylglutaconicaciduria, type 3$ |
N/A |
N/A |
No information
|
| $3-methylglutaconic aciduria, type V$ |
N/A |
N/A |
No information
|
| Barth Syndrome |
approx 1 in 400,000 or 0.00% or 680 people in USA |
680 |
1 per 200,000 male infants suffer from 2-methylglutaconic aciduria type 2, Genetics Home Reference website
|
| Randall disease |
N/A |
N/A |
No information
|
| Glomerulonephritis -- sparse hair -- telangiectases |
N/A |
N/A |
No information
|
| Fanconi renotubular syndrome |
N/A |
N/A |
No information
|
| Nephrotic syndrome, idiopathic, steroid-resistant, familial |
N/A |
N/A |
No information
|
| Nephrosis, idiopathic form, familial |
N/A |
N/A |
No information
|
| Nephrotic syndrome, idiopathic, steroid-resistant, autosomal recessive |
N/A |
N/A |
No information
|
| Nephrotic syndrome type 2 |
N/A |
N/A |
No information
|
| Nephrotic syndrome, early onset, type 3 |
N/A |
N/A |
No information
|
| Nephrotic syndrome, steroid-sensitive |
N/A |
N/A |
No information
|
| Nephrosis, idiopathic, sporadic form |
N/A |
N/A |
No information
|
| Nephrotic syndrome, steroid-resistant, sporadic idiopathic |
N/A |
N/A |
No information
|
| Microcephaly, hiatal hernia and nephrotic syndrome |
N/A |
N/A |
No information
|
| Nephrotic syndrome ocular anomalies |
N/A |
N/A |
No information
|
| Polyomavirus allograft nephropathy |
N/A |
N/A |
No information
|
| Mesangial sclerosis, diffuse |
N/A |
N/A |
No information
|
| Renal dysplasia, diffuse cystic |
N/A |
N/A |
No information
|
| Nephrosclerosis |
N/A |
N/A |
No information
|
| Idiopathic minimal change nephrotic syndrome |
N/A |
N/A |
No information
|
| Papillary renal cell carcinoma |
N/A |
N/A |
No information
|
| Acute Renal Failure |
N/A |
N/A |
No information
|
| Patau syndrome |
N/A |
N/A |
No information
|
| Phenylketonuria |
approx 1 in 10,000 or 0.01% or 27,200 people in USA |
27,199 |
1 per 10,000 - 15,000 newborns are diagnosed with phenylketonuria in the US, Genetics Home Reference website
|
| Fructosuria |
N/A |
N/A |
No information
|
| Lipoprotein glomerulopathy |
N/A |
N/A |
No information
|
| Nephropathy familial with hyperuricemia |
N/A |
N/A |
No information
|
| Inborn branched chain aminoaciduria |
N/A |
N/A |
No information
|
| Chronic interstitial nephritis |
N/A |
N/A |
No information
|
| Hypomagnesemia 4, renal |
N/A |
N/A |
No information
|
| Glomerulonephritis, membranous congenital due to anti-maternal NEP alloimmunisation |
N/A |
N/A |
No information
|
| Medullary sponge kidney and anodontia of permanent dentition |
N/A |
N/A |
No information
|
| Glucosuria |
N/A |
N/A |
No information
|
| Megalocytic interstitial nephritis |
N/A |
N/A |
No information
|
| Mesangiocapillary glomerulonephritis type 1 |
N/A |
N/A |
No information
|
| Primary hyperoxaluria type 2 |
N/A |
N/A |
No information
|
| Primary hyperoxaluria type 1 |
N/A |
N/A |
No information
|
| Methylmalonic aciduria -- homocystinuria |
N/A |
N/A |
No information
|
| Hyperdibasic aminoaciduria type 2 |
N/A |
N/A |
No information
|
| Methylmalonic acidemia -- homocystinuria |
N/A |
N/A |
No information
|
| Methylmalonicaciduria, vitamin B12 unresponsive, mut 0 |
N/A |
N/A |
No information
|
| Methylmalonicaciduria, vitamin B12 unresponsive, mut - |
N/A |
N/A |
No information
|
| Aminoaciduria, Renal |
N/A |
N/A |
No information
|
| Beta-hydroxybutyric aciduria |
N/A |
N/A |
No information
|
| Isobutyric aciduria |
N/A |
N/A |
No information
|
| Glutaric aciduria 2 |
N/A |
N/A |
No information
|
| $2-Methylbutyric Aciduria$ |
N/A |
N/A |
No information
|
| Orotic aciduria purines-pyrimidines |
N/A |
N/A |
No information
|
| Aminoaciduria |
N/A |
N/A |
No information
|
| Argininosuccinic aciduria |
N/A |
N/A |
No information
|
| Ethylmalonic aciduria |
approx 1 in 200,000,000 or 0.00% or 1 people in USA |
1 |
about 30 cases of ethylmalonic encephalopathy have been reported worldwide, Genetics Home Reference website
|
| Malonic aciduria |
approx 1 in 13,600,000 or 0.00% or 20 people in USA |
20 |
less than 20 cases of malonic aciduria have been reported, Genetics Home Reference website
|
| Glutaricaciduria I |
approx 1 in 300 or 0.33% or 906,666 people in USA |
906,666 |
estimated 1 per 300 people from the Ojibwa population of Canada suffer from glutaric academia type I, Genetics Home Reference website
|
| Glutaric Aciduria, neonatal form of type II A |
N/A |
N/A |
No information
|
| Dibasic aminoaciduria 2 |
N/A |
N/A |
No information
|
| $2-Hydroxyglutaricaciduria$ |
N/A |
N/A |
No information
|
| Orotic aciduria hereditary |
N/A |
N/A |
No information
|
| $3-Hydroxyisobutyric aciduria$ |
N/A |
N/A |
No information
|
| Fumaric aciduria |
N/A |
N/A |
No information
|
| Dibasic aminoaciduria type 1 |
N/A |
N/A |
No information
|
| Glutaricaciduria type 3 |
N/A |
N/A |
No information
|
| $4-hydroxyphenylacetic aciduria$ |
N/A |
N/A |
No information
|
| Magnesium wasting renal |
N/A |
N/A |
No information
|
| Diffuse leiomyomatosis with Alport syndrome |
N/A |
N/A |
No information
|
| Methylmalonicacidemia with homocystinuria, cbl D |
N/A |
N/A |
No information
|
| Molybdenum, cofactor deficiency, inherited |
N/A |
N/A |
No information
|
| Oroticaciduria 1 |
N/A |
N/A |
No information
|
| Xanthinuria |
N/A |
N/A |
No information
|
| Glutaricaciduria 2B |
N/A |
N/A |
No information
|
| Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome |
N/A |
N/A |
estimated less than 100 people have been reportd with ornithine translocase deficiency worldwide, Genetics Home Reference website
|
| Glutathionuria |
N/A |
N/A |
No information
|
| Inherited Hemolytic-Uremic Syndrome |
N/A |
N/A |
No information
|
| Chromophobe renal cell carcinoma |
N/A |
N/A |
No information
|
| Clear cell renal cell carcinoma |
N/A |
N/A |
No information
|
| Chromophil renal cell carcinoma |
N/A |
N/A |
No information
|
| Familial renal cell carcinoma |
N/A |
N/A |
No information
|
| Renal Cell Carcinoma Associated with Neuroblastoma |
N/A |
N/A |
No information
|
| Hereditary Leiomyomatosis and Renal Cell Cancer |
N/A |
N/A |
No information
|
| Renal Cell Carcinoma 2 |
N/A |
N/A |
No information
|
| Renal Cell Carcinoma 3 |
N/A |
N/A |
No information
|
| Renal Cell Carcinoma 4 |
N/A |
N/A |
No information
|
| Intrathoracic kidney -- vertebral fusion |
N/A |
N/A |
No information
|
| Aplastic anemia -- paroxysmal nocturnal hemoglobinuria syndrome |
N/A |
N/A |
No information
|
| Hemoglobinuria |
N/A |
N/A |
No information
|
| Paroxysmal Nocturnal Hemoglobinuria |
N/A |
N/A |
No information
|
| Hemorragic fever with renal syndrome |
N/A |
N/A |
No information
|
| The clap |
N/A |
N/A |
No information
|
| Honeymoon Bladder |
N/A |
N/A |
No information
|
| Renal zygmycosis |
N/A |
N/A |
No information
|
| Hypomagnesemia with hypocalciuria |
N/A |
N/A |
No information
|
| Membranoproliferative glomerulonephritis (type 2) |
N/A |
N/A |
No information
|
| Membranoproliferative glomerulonephritis, X-linked |
N/A |
N/A |
No information
|
| Glomerulonephritis, membranous congenital due to anti-maternal neutral endopeptidase alloimmunisation |
N/A |
N/A |
No information
|
| Immunotactoid glomerulonephritis |
N/A |
N/A |
No information
|
| Membranoproliferative glomerulonephritis |
N/A |
N/A |
No information
|
| Cystinuria -- lysinuria |
N/A |
N/A |
No information
|
| Xanthic urolithiasis |
N/A |
N/A |
No information
|
| Nephrolithiasis type 1 |
N/A |
N/A |
No information
|
| Nephrolithiasis type 2 |
N/A |
N/A |
No information
|
| Glutaric aciduria type II |
N/A |
N/A |
No information
|
| Hyperimidodipeptiduria |
N/A |
N/A |
No information
|
| Mevalonic aciduria |
N/A |
N/A |
No information
|
| Vitamin D resistant rickets |
N/A |
N/A |
No information
|
| Rhabdoid tumor |
N/A |
N/A |
No information
|
| Wilms tumour and pseudohermaphroditism |
N/A |
N/A |
No information
|
| Collecting duct carcinoma |
N/A |
N/A |
No information
|
| Transitional cell carcinoma |
N/A |
N/A |
No information
|
| Urosepsis |
N/A |
N/A |
No information
|
| Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor |
N/A |
N/A |
No information
|
| Renal pelvis and ureter, transitional cell cancer |
N/A |
N/A |
No information
|
| Nephroblastomatosis -- fetal ascites -- macrosomia -- wilms tumor |
N/A |
N/A |
No information
|
| Gonococcal urethritis |
N/A |
N/A |
No information
|
| Hepatorenal tyrosinemia |
approx 1 in 1,845 or 0.05% or 147,345 people in USA |
147,345 |
1 per 1,846 people from the Saguenay-La St. Jean region of Quebec suffer from tyrosinemia type 1, Genetics Home Reference website
|
| Membranous nephropathy, idiopathic |
N/A |
N/A |
No information
|
| Hyperphenylalaninemia with primapterinuria |
N/A |
N/A |
No information
|
| Oncocytoma, renal |
N/A |
N/A |
No information
|
| Hypoketonemic hypoglycemia |
N/A |
N/A |
No information
|
| Classical Potter syndrome |
N/A |
N/A |
No information
|
| Potter syndrome type 2 |
N/A |
N/A |
No information
|
| Potter syndrome type 4 |
N/A |
N/A |
No information
|
| Potter syndrome |
N/A |
N/A |
No information
|
| Hypomagnesemia with normocalciuria |
N/A |
N/A |
No information
|
| Saccharopinuria |
N/A |
N/A |
No information
|
| Aspartylglycosaminuria |
N/A |
N/A |
No information
|
| Renal glycosuria |
N/A |
N/A |
No information
|
| Homocytsinuria due to defect in methylation cbl e |
N/A |
N/A |
No information
|
| Phenylketonuria type 2 |
N/A |
N/A |
No information
|
| Sialuria syndrome |
N/A |
N/A |
No information
|
| Hydroxykynureninuria |
N/A |
N/A |
No information
|
| Hypercalciuria, childhood idiopathic |
N/A |
N/A |
No information
|
| Iminoglycinuria |
N/A |
N/A |
No information
|
| Sialuria, French type |
N/A |
N/A |
No information
|
| Methylmalonic aciduria -- microcephaly -- cataract |
N/A |
N/A |
No information
|
| Inborn renal aminoaciduria |
N/A |
N/A |
No information
|
| Pentosuria |
N/A |
N/A |
No information
|
| Mauriac syndrome |
N/A |
N/A |
No information
|
| Renal glucosuria |
N/A |
N/A |
No information
|
| Seizures -- intellectual deficit due to hydroxylysinuria |
N/A |
N/A |
No information
|
| Hypotonia-cystinuria syndrome |
N/A |
N/A |
No information
|
| Sialuria, Finnish type |
N/A |
N/A |
No information
|
| Urinary tract neoplasm |
N/A |
N/A |
No information
|
| Cope's syndrome |
N/A |
N/A |
No information
|
| Medullary cystic kidney disease 1 |
N/A |
N/A |
No information
|
| Medullary cystic kidney disease 2 |
N/A |
N/A |
No information
|
| Medullary cystic kidney disease, autosomal recessive |
N/A |
N/A |
No information
|
| Toni-Fanconi syndrome type 1 |
N/A |
N/A |
No information
|
| Spondyloepiphyseal dysplasia -- nephrotic syndrome |
N/A |
N/A |
No information
|
| Spondyloepiphyseal dysplasia -- nephritic syndrome |
N/A |
N/A |
No information
|
| Armani-Ebstein nephropathy |
N/A |
N/A |
No information
|
| Acute tubulointerstitial nephritis and uveitis syndrome |
N/A |
N/A |
No information
|
| Angiopathy, hereditary, with nephropathy, aneurysms and muscle cramps |
N/A |
N/A |
No information
|
| Coloboma porencephaly hydronephrosis |
N/A |
N/A |
No information
|
| Nephronophtisis familial, adult form -- spastic quadriparesia |
N/A |
N/A |
No information
|
| Mesangiocapillary glomerulonephritis type III |
N/A |
N/A |
No information
|
| Nephropathic cystinosis |
N/A |
N/A |
No information
|
| Finnish nephrosis syndrome |
N/A |
N/A |
No information
|
| Congenital mesoblastic nephroma |
N/A |
N/A |
No information
|
| Tubulointerstitial nephritis and uveitis |
N/A |
N/A |
No information
|
| Oligomeganephronic renal hypoplasia |
N/A |
N/A |
No information
|
| Nephrogenic Fibrosing Dermopathy |
N/A |
N/A |
No information
|
| Hydronephrosis congenital |
N/A |
N/A |
No information
|
| Multicystic renal dysplasia, bilateral |
N/A |
N/A |
No information
|
| Danubian endemic familial nephropathy |
N/A |
N/A |
No information
|
| Inverted smile -- occult nephropathic bladder |
N/A |
N/A |
No information
|
| Hydronephrosis with Peculiar Facies |
N/A |
N/A |
No information
|
| Renal dysplasia diffuse autosomal recessive |
N/A |
N/A |
No information
|
| Multicystic Renal Dysplasia |
N/A |
N/A |
No information
|
| Collagen type III glomerulopathy |
N/A |
N/A |
No information
|
| Renal colic |
N/A |
N/A |
No information
|
| Bilateral Renal Agenesis |
N/A |
N/A |
No information
|
| Optic nerve coloboma with renal disease |
N/A |
N/A |
No information
|
| Renal dysplasia -- limb defects syndrome |
N/A |
N/A |
No information
|
| Renal adysplasia dominant type |
N/A |
N/A |
No information
|
| Renal rickets |
N/A |
N/A |
No information
|
| Bilateral renal agenesis dominant type |
N/A |
N/A |
No information
|
| Renal agenesis, bilateral |
N/A |
N/A |
No information
|
| Renal nutcracker syndrome |
N/A |
N/A |
No information
|
| Glomerulopathy with fibronectin deposits |
N/A |
N/A |
No information
|
| Focal segmental glomerulosclerosis |
N/A |
N/A |
No information
|
| Anti-glomerular basement membrane antibody-mediated disease |
N/A |
N/A |
No information
|
| Pseudohypoaldosteronism type 1, autosomal dominant |
N/A |
N/A |
No information
|
| Pseudohypoaldosteronism type 1, autosomal recessive |
N/A |
N/A |
No information
|
| Vesicoureteral Reflux 2 |
N/A |
N/A |
No information
|
| Vesicoureteral Reflux 1 |
N/A |
N/A |
No information
|
| Aphalangy -- hemivertebrae -- urogenital-intestinal dysgenesis |
N/A |
N/A |
No information
|
| Gullner Syndrome |
N/A |
N/A |
No information
|
| Apparent mineralocorticoid excess |
N/A |
N/A |
No information
|
| Precalicial canalicular ectasia |
N/A |
N/A |
No information
|
| Brachydactyly, absent pectoral muscles and agenesis/hypoplasia of kidneys |
N/A |
N/A |
No information
|
| Morning Glory Fundus Anomaly -- Optic Nerve Coloboma -- Porencephaly -- Hydronephrosis |
N/A |
N/A |
No information
|
| Leiomyomatosis of oesophagus, congenital cataract and hematuria |
N/A |
N/A |
No information
|
| Pierson Syndome |
N/A |
N/A |
No information
|
| Cerebral calcifications opalescent teeth phosphaturia |
N/A |
N/A |
No information
|
| Epstein's Syndrome |
N/A |
N/A |
No information
|
| Urogenital dysplasia |
N/A |
N/A |
No information
|
| Apparent Mineralocorticoid Excess, type 2 |
N/A |
N/A |
No information
|
| Torticollis, keloids, cryptorchidism, renal dysplasia |
N/A |
N/A |
No information
|
| HARD syndrome (Hydrocephalus -- agyria -- retinal dysplasia) |
N/A |
N/A |
No information
|
| Wolfram's disease |
N/A |
N/A |
No information
|
| Alport syndrome -- mental retardation -- midface hypoplasia -- elliptocytosis |
N/A |
N/A |
No information
|
| Alport syndrome with macrothrombocytopenia |
N/A |
N/A |
No information
|
| Alport Syndrome |
approx 1 in 50,000 or 0.00% or 5,440 people in USA |
5,440 |
1 per 50,000 newborns suffer from Alport syndrome, Genetics Home Reference website
|
| Alport syndrome, recessive type |
N/A |
N/A |
No information
|
| Dent syndrome |
N/A |
N/A |
No information
|
| Hereditary primary Fanconi disease |
N/A |
N/A |
No information
|
| Fanconi syndrome |
N/A |
N/A |
No information
|
| Alport syndrome, dominant type |
N/A |
N/A |
No information
|
| Urophathy distal obstructive polydactyly |
N/A |
N/A |
No information
|
| Phocomelia -- thrombocytopenia -- encephalocele -- urogenital malformation |
N/A |
N/A |
No information
|
| Frontonasal dysplasia -- phocomelic upper limbs |
N/A |
N/A |
No information
|
| Ectrodactyly-ectodermal dysplasia-cleft lip/cleft palate |
N/A |
N/A |
No information
|
| Oculo-cerebro-acral, (Roberts-like)-ectrodactyly |
N/A |
N/A |
No information
|
| Acro-pectoro-renal field defect |
N/A |
N/A |
No information
|
| Mesodermal defects lower type |
N/A |
N/A |
No information
|
| Spondylocostal dysostosis with anal atresia and urogenital anomalies |
N/A |
N/A |
No information
|
| Cervical ribs, sprengel anomaly, anal atresia, urethral obstruction |
N/A |
N/A |
No information
|
| Jejunal atresia with renal adysplasia |
N/A |
N/A |
No information
|
| Atresia of urethra |
N/A |
N/A |
No information
|
| Amelogenesis Imperfeca, Hypoplastic, and Nephrocalcinosis |
N/A |
N/A |
No information
|
| Duplication of urethra |
N/A |
N/A |
No information
|
| Multiple congenital anomalies -- mental retardation -- growth failure and cleft lip/ palate |
N/A |
N/A |
No information
|
| Uropathy distal obstructive polydactyly |
N/A |
N/A |
No information
|
| Fanconi pancytopenia |
N/A |
N/A |
No information
|
| Acrorenal syndrome |
N/A |
N/A |
No information
|
| Alport syndrome with leukocyte inclusions and macrothrombocytopenia |
N/A |
N/A |
No information
|
| Diaphanospondylodysostosis |
N/A |
N/A |
No information
|
| Absent patellae -- scrotal hypoplasia -- renal anomalies -- facial dysmorphism -- mental retardation |
N/A |
N/A |
No information
|
| Urethral obstruction sequence |
N/A |
N/A |
No information
|
| Camptodactyly -- taurinuria |
N/A |
N/A |
No information
|
| Hemolytic uremic syndrome |
N/A |
N/A |
No information
|
| Hemolytic uremic syndrome, atypical, childhood |
N/A |
N/A |
No information
|
| D-minus hemolytic uremic syndrome (D-HUS) -- pregnancy related |
N/A |
N/A |
No information
|
| D-plus hemolytic uremic syndrome (D+HUS) |
N/A |
N/A |
No information
|
| Atypical hemolytic uremic syndrome |
N/A |
N/A |
No information
|
| D-minus hemolytic uremic syndrome (D-HUS) -- familial |
N/A |
N/A |
No information
|
| Microcephaly -- glomerulonephritis -- Marfanoid habitus |
N/A |
N/A |
No information
|
| Hepatorenal Syndrome |
N/A |
N/A |
No information
|
| Goodpasture's syndrome |
N/A |
N/A |
No information
|
| HARD syndrome |
N/A |
N/A |
No information
|
| VATER association |
N/A |
N/A |
No information
|
| Whelan syndrome |
N/A |
N/A |
No information
|
| Cloacal exstrophy |
N/A |
N/A |
No information
|
| Loin pain, hematuria syndrome |
N/A |
N/A |
No information
|
| Ischiadic hypoplasia -- renal dysfunction -- immunodeficiency |
N/A |
N/A |
No information
|
| VACTERL with hydrocephalus, X-linked |
N/A |
N/A |
No information
|
| VACTERL association |
N/A |
N/A |
No information
|
| VACTERYL hydrocephaly |
N/A |
N/A |
No information
|
| VACTERL association with hydrocephaly, X-linked |
N/A |
N/A |
No information
|
| Pseudohypoaldosteronism type 1 |
N/A |
N/A |
No information
|
| Pseudoaldosteronism |
N/A |
N/A |
No information
|
| Pseudohyperaldosteronism |
N/A |
N/A |
No information
|
| Pseudohypoaldosteronism |
N/A |
N/A |
No information
|
| Pseudohypoaldosteronism type II |
N/A |
N/A |
No information
|
| Non-diarrheal (D-) HUS syndrome |
N/A |
N/A |
No information
|
| Senior-Loken syndrome 5 |
N/A |
N/A |
No information
|
| Senior-Loken syndrome 6 |
N/A |
N/A |
No information
|
| Senior-Loken Syndrome |
N/A |
N/A |
No information
|
| Senior-Loken syndrome 4 |
N/A |
N/A |
No information
|
| Senior-Loken syndrome 3 |
N/A |
N/A |
No information
|
| Senior-Loken syndrome 1 |
N/A |
N/A |
No information
|
| Congenital megalo-ureter |
N/A |
N/A |
No information
|
| Digitorenocerebral syndrome |
N/A |
N/A |
No information
|
| Cystic hamartoma of lung and kidney |
N/A |
N/A |
No information
|
| Rudd-Klimek syndrome |
N/A |
N/A |
No information
|
| Thymic-Renal-Anal-Lung dysplasia |
N/A |
N/A |
No information
|
| Meckel syndrome type 2 |
N/A |
N/A |
No information
|
| Nephrosis -- deafness -- urinary tract -- digital malformation |
N/A |
N/A |
No information
|
| Meckel Syndrome |
N/A |
N/A |
No information
|
| Meckel syndrome type 3 |
N/A |
N/A |
No information
|
| Meckel syndrome, type 5 |
N/A |
N/A |
No information
|
| Dyschondrosteosis -- nephritis |
N/A |
N/A |
No information
|
| Oculorenocerebellar syndrome |
N/A |
N/A |
No information
|
| Neurofaciodigitorenal syndrome |
N/A |
N/A |
No information
|
| Aniridia -- renal agenesis -- psychomotor retardation |
N/A |
N/A |
No information
|
| Malakoplakia |
N/A |
N/A |
No information
|
| Primary tubular proximal acidosis |
N/A |
N/A |
No information
|
| Infantile idiopathic hypercalciuria, congenital myopia, macular coloboma |
N/A |
N/A |
No information
|
| Arachnodactyly -- ataxia -- cataract -- aminoaciduria -- mental retardation |
N/A |
N/A |
No information
|
| Kidney arteriovenous fistula |
N/A |
N/A |
No information
|
| Familial hematuria, autosomal dominant -- retinal arteriolar tortuosity -- contractures |
N/A |
N/A |
No information
|
| Unusual facies, hepatic fibrosis, renal cysts and mental retardation |
N/A |
N/A |
No information
|
| Unusual facies, renal and Mullerian hypoplasia and severe somatic and mental retardation |
N/A |
N/A |
No information
|
| Infundibulopelvic stenosis multicystic kidney |
N/A |
N/A |
No information
|
| Anemic -- hematuria syndrome |
N/A |
N/A |
No information
|
| Hemorrhagic shock and encephalopathy syndrome |
N/A |
N/A |
No information
|
| Acrofrontofacionasal dysostosis syndrome |
N/A |
N/A |
No information
|
| Megacystis microcolon -- intestinal hypoperistalsis -- hydronephrosis |
N/A |
N/A |
No information
|
| Analgesic syndrome |
N/A |
N/A |
No information
|
| Bladder immaturity syndrome |
N/A |
N/A |
No information
|
| HERNS syndrome |
N/A |
N/A |
No information
|
| Female sex reversal with dysgenesis of kidneys, adrenals and lungs |
N/A |
N/A |
No information
|
| Angiomyolipoma |
N/A |
N/A |
No information
|
| Mayer-Rokitansky-Kuster-Hauser, syndrome, type 2 (MRKH type 2) |
N/A |
N/A |
No information
|
| Toe syndactyly, telecanthus, and anogenital and renal malformations |
N/A |
N/A |
No information
|
| Cystocele |
N/A |
N/A |
No information
|
| Reiter’s syndrome |
N/A |
N/A |
No information
|
| Goodpasture syndrome |
N/A |
N/A |
rare.
|
| Primary Hyperaldosteronism |
N/A |
N/A |
No information
|
| Stones |
N/A |
N/A |
No information
|
| Uremia |
N/A |
N/A |
No information
|
| Brachymesomelia-renal syndrome |
N/A |
N/A |
No information
|
| Cerebrorenodigital syndrome |
N/A |
N/A |
No information
|
| Denys-Drash Syndrome |
N/A |
N/A |
No information
|
| MURCS Association |
N/A |
N/A |
No information
|
| Schinzel Giedion Syndrome |
N/A |
N/A |
No information
|
| Antley-Bixler Syndrome |
N/A |
N/A |
No information
|
| Lowe Syndrome |
N/A |
N/A |
No information
|
| Alstrom syndrome |
N/A |
N/A |
No information
|
| Nager Syndrome |
N/A |
N/A |
No information
|
| Laurence-Moon Syndrome |
N/A |
N/A |
No information
|
| Mullerian Aplasia -- Renal Aplasia -- Cervicothoracic Somite Dysplasia |
N/A |
N/A |
No information
|
| Aniridia ataxia renal agenesis psychomotor retardation |
N/A |
N/A |
No information
|
| Friedel Heid Grosshans syndrome |
N/A |
N/A |
No information
|
| Thyrocerebral-retinal syndrome |
N/A |
N/A |
No information
|
| Cutler Syndrome |
N/A |
N/A |
No information
|
| Brosnan Syndrome |
N/A |
N/A |
No information
|
| Hinman syndrome |
N/A |
N/A |
No information
|
| Leucinosis |
N/A |
N/A |
No information
|
| Daentl-Townsend-Siegel syndrome |
N/A |
N/A |
No information
|
| Rudiger syndrome |
N/A |
N/A |
No information
|
| Southworth symptom complex |
N/A |
N/A |
No information
|
| Spastic pelvic floor syndrome |
N/A |
N/A |
No information
|
| Stauffer syndrome |
N/A |
N/A |
No information
|
| Wohlmann-Caglkar syndrome |
N/A |
N/A |
No information
|
| Abderhalden-Kaufmann-Lignac syndrome |
N/A |
N/A |
No information
|
| BEEC |
N/A |
N/A |
No information
|
| Bladder Exstrophy-Epispadias-Cloacal Exstrophy Complex |
N/A |
N/A |
No information
|
| Boichis syndrome |
N/A |
N/A |
No information
|
| BOR syndrome |
N/A |
N/A |
No information
|
| Lightwood-Albright syndrome |
N/A |
N/A |
No information
|
| Munk disease |
N/A |
N/A |
No information
|
| Exstrophy of the bladder |
N/A |
N/A |
No information
|
| Billet-Bear syndrome |
N/A |
N/A |
No information
|
| Hardikar syndrome |
N/A |
N/A |
No information
|
| Alsing syndrome |
N/A |
N/A |
No information
|
| Renoanogenital syndrome |
N/A |
N/A |
No information
|
| Crawfurd syndrome |
N/A |
N/A |
No information
|
| Acrorenal syndrome recessive |
N/A |
N/A |
No information
|
| Kallikrein hypertension |
N/A |
N/A |
No information
|
| Gorlin-Bushkell-Jensen syndrome |
N/A |
N/A |
No information
|
| Conorenal Syndrome |
N/A |
N/A |
No information
|
| Crystal deposit disease |
N/A |
N/A |
No information
|
| Exstrophy of the bladder -- epispadias |
N/A |
N/A |
No information
|
| Fraser-Jequier-Chen syndrome |
N/A |
N/A |
No information
|
| Infundibulopelvic dysgenesis |
N/A |
N/A |
No information
|
| Cerebrorenodigital syndrome with limb malformations and triradiate acetabula |
N/A |
N/A |
No information
|
| Johnson-Munson syndrome |
N/A |
N/A |
No information
|
| Amastia, bilateral, with ureteral triplication and dysmorphism |
N/A |
N/A |
No information
|
| Blum's syndrome |
N/A |
N/A |
No information
|
| Bamberger albuminuria (obsolete term) |
N/A |
N/A |
No information
|
| Bosviel syndrome |
N/A |
N/A |
No information
|
| Braun-Bayer syndrome |
N/A |
N/A |
No information
|
| Denys-Corbeel syndrome |
N/A |
N/A |
No information
|
| Fenwick ulcer |
N/A |
N/A |
No information
|
| Foix-Alajouanine syndrome |
N/A |
N/A |
No information
|
| Pfeiffer-Hirschfelder-Rott syndrome |
N/A |
N/A |
No information
|
| Myoglobinuria recurrent |
N/A |
N/A |
No information
|
| Renoprival hypertension |
N/A |
N/A |
No information
|
| Situs inversus totalis with cystic dysplasia of kidneys and pancreas |
N/A |
N/A |
No information
|
| Rayner-Lampert-Rennert syndrome |
N/A |
N/A |
No information
|
| Myoglobinuria, dominant form |
N/A |
N/A |
No information
|
| RHYNS syndrome |
N/A |
N/A |
No information
|
| Allanson-Pantzar-McLeod syndrome |
N/A |
N/A |
No information
|
| Passos-Bueno syndrome |
N/A |
N/A |
No information
|
| Posterior valve, urethra |
N/A |
N/A |
No information
|
| Fitzsimmons-Walson-Mellor syndrome |
N/A |
N/A |
No information
|
| Radio renal syndrome |
N/A |
N/A |
No information
|
| Corpus callosum agenesis -- double urinary collecting system |
N/A |
N/A |
No information
|
| FLOTCH syndrome |
N/A |
N/A |
No information
|
| Feigenbaum-Bergeron-Richardson syndrome |
N/A |
N/A |
No information
|
| Meier-Blumberg-Imahorn syndrome |
N/A |
N/A |
No information
|
| Lachiewicz-Sibley syndrome |
N/A |
N/A |
No information
|
| Thomas syndrome |
N/A |
N/A |
No information
|
| Faciooculoacousticorenal syndrome |
N/A |
N/A |
No information
|
| Oculo skeletal renal syndrome |
N/A |
N/A |
No information
|
| Say-Carpenter syndrome |
N/A |
N/A |
No information
|
| Axial mesodermal dysplasia spectrum |
N/A |
N/A |
No information
|
| Czeizel-Losonci syndrome |
N/A |
N/A |
No information
|
| Fowler-Christmas-Chapple syndrome |
N/A |
N/A |
No information
|
| Cerebro oculo skeleto renal syndrome |
N/A |
N/A |
No information
|
| Edwards-Patton-Dilly syndrome |
N/A |
N/A |
No information
|
| Saito-Kuba-Tsuruta syndrome |
N/A |
N/A |
No information
|
| Karandikar-Maria-Kamble syndrome |
N/A |
N/A |
No information
|
| Selig-Benacerraf-Greene syndrome |
N/A |
N/A |
No information
|
| Rambaud-Galian syndrome |
N/A |
N/A |
No information
|
| Salcedo syndrome |
N/A |
N/A |
No information
|
| Daneman Davy Mancer syndrome |
N/A |
N/A |
No information
|
| Fried-Goldberg-Mundel syndrome |
N/A |
N/A |
No information
|
| Oculo cerebro acral syndrome |
N/A |
N/A |
No information
|
| Steinfeld syndrome |
N/A |
N/A |
No information
|
| Fukuda-Miyanomae-Nakata syndrome |
N/A |
N/A |
No information
|
| Frasier syndrome |
N/A |
N/A |
No information
|
| Palmer-Pagon syndrome |
N/A |
N/A |
No information
|
| Pierson syndrome |
N/A |
N/A |
No information
|
| Daentl-Towsend-Siegel syndrome |
N/A |
N/A |
No information
|
| Ellis-Yale-Winter syndrome |
N/A |
N/A |
No information
|
| Thompson-Baraitser syndrome |
N/A |
N/A |
No information
|
| Okamuto Satomura syndrome |
N/A |
N/A |
No information
|
| Renal-genital-middle ear anomalies |
N/A |
N/A |
No information
|
| Schmitt-Gillenwater-Kelly syndrome |
N/A |
N/A |
No information
|
| Renal caliceal diverticuli -- deafness |
N/A |
N/A |
No information
|
| Dent's disease |
N/A |
N/A |
No information
|
| Manz syndrome |
N/A |
N/A |
No information
|
| Rowley-Rosenberg syndrome |
N/A |
N/A |
No information
|
| Myoglobinuria |
N/A |
N/A |
No information
|
| Alstrom disease |
approx 1 in 14,117,646 or 0.00% or 19 people in USA |
19 |
about 425 cases of Alstrom disease reported worldwide, Genetics Home Reference website
|
| BOR-Duane hydrocephalus contiguous gene syndrome |
N/A |
N/A |
No information
|
| Bhaskar-Jagannathan syndrome |
N/A |
N/A |
No information
|
| Carnevale-Canun-Mendoza syndrome |
N/A |
N/A |
No information
|
| Baraitser-Rodeck-Garner syndrome |
N/A |
N/A |
No information
|
| Ben-Ari-Shuper-Mimouni syndrome |
N/A |
N/A |
No information
|
| Kashani-Strom-Utley syndrome |
N/A |
N/A |
No information
|
| Lower limb anomaly -- ureteral obstruction |
N/A |
N/A |
No information
|
| Faciocardiorenal syndrome |
N/A |
N/A |
No information
|
| Stimmler syndrome |
N/A |
N/A |
No information
|
| Thieffry and Sorrell Dejerine syndrome |
N/A |
N/A |
No information
|
| Alopecia, epilepsy, oligophrenia syndrome of Moynahan |
N/A |
N/A |
No information
|
| Adrenomyodystrophy |
N/A |
N/A |
No information
|
| Lutz-Richner-Landolt syndrome |
N/A |
N/A |
No information
|
| AREDYLD |
N/A |
N/A |
No information
|
| Barakat syndrome |
N/A |
N/A |
No information
|
| Acrorenal mandibular syndrome |
N/A |
N/A |
No information
|
| GOMBO syndrome |
N/A |
N/A |
No information
|
| Epstein (C.J.) syndrome |
N/A |
N/A |
No information
|
| Megacystis microcolon intestinal hypoperistalsis syndrome |
N/A |
N/A |
No information
|
| Drash syndrome |
N/A |
N/A |
No information
|
| Oxalosis, type I |
approx 1 in 60,000 or 0.00% or 4,533 people in USA |
4,533 |
estimated 1 per 60,000 - 120,000 births are affected by primary hyperoxaluria, type I, Genetics Home Reference website
|
| Muckle-Wells syndrome |
N/A |
N/A |
No information
|
| Lowe oculocerebrorenal syndrome |
N/A |
N/A |
No information
|
| Bright's Disease |
N/A |
N/A |
No information
|
| Collagenoma, cutaneous familial |
N/A |
N/A |
No information
|
| Dahlberg syndrome |
N/A |
N/A |
No information
|
| Fechtner syndrome |
N/A |
N/A |
No information
|
| Herrmann syndrome |
N/A |
N/A |
No information
|
| Kelley-Seegmiller syndrome |
N/A |
N/A |
No information
|
| Krause-Kivlin syndrome |
N/A |
N/A |
No information
|
| Melnick-Fraser syndrome |
N/A |
N/A |
No information
|
| Craniosynostosis radial aplasia syndrome |
N/A |
N/A |
No information
|
| Urorectal septum malformation sequence |
N/A |
N/A |
No information
|
| Urogenital adysplasia |
N/A |
N/A |
No information
|
| Urogenital adysplasia, hereditary |
N/A |
N/A |
No information
|
| Urban Schosser Spohn syndrome |
N/A |
N/A |
No information
|
| Urachal cyst |
N/A |
N/A |
No information
|
| Urofacial syndrome |
N/A |
N/A |
No information
|
| Oxalosis |
N/A |
N/A |
No information
|
| Gitelman syndrome |
N/A |
N/A |
No information
|
| Pseudophosphatasia |
N/A |
N/A |
No information
|
| Acro-reno-ocular syndrome |
N/A |
N/A |
No information
|
| Oxalosis, Type II |
N/A |
N/A |
No information
|
| Intermediate cystinosis |
N/A |
N/A |
No information
|
The medical term 'prevalence' of Urinary system conditions usually refers to the estimated population
of people who are managing Urinary system conditions at any given time,
whereas the annual diagnosis rate of new cases of Urinary system conditions is called the 'incidence'.
For more information on prevalence and incidence statistics, see about prevalence and incidence statistics.
