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Prevalence Statistics for Types of Urinary system conditions

Prevalence Statistics for Types of Urinary system conditions

The information below shows a list of types of Urinary system conditions, with information as to the prevalence of each of these types. Estimates of the people affected are calculated based on the available statistic.

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
Reiterís 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

Types of Urinary system conditions

For more information about types of Urinary system conditions, refer to our section on types of Urinary system conditions.

About prevalence:

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.



Footnotes:
1. Rose and Mackay, 1998, The Autoimmune Diseases, Third Edition

 

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