ureteral disease +
bladder disease +
kidney disease +
amino acid metabolic disorder +

2-aminoadipic 2-oxoadipic aciduria
2-hydroxyglutaric aciduria +
3-hydroxy-3-methylglutaryl-CoA lyase deficiency
3-hydroxyisobutryl-CoA hydrolase deficiency
3-methylcrotonyl-CoA carboxylase deficiency +
adenylosuccinase lyase deficiency
alkaptonuria
anuria
apolipoprotein A-IV associated amyloidosis
argininosuccinic aciduria
atheroembolism of kidney
beta-ketothiolase deficiency
bladder benign neoplasm +
bladder calculus
bladder carcinoma in situ
bladder diverticulum +
bladder exstrophy
bladder neck obstruction
bladder tuberculosis
branched-chain keto acid dehydrogenase kinase deficiency
Brunner Syndrome
cerebral creatine deficiency syndrome +
congenital glutamine deficiency
congenital megabladder
cystathioninuria
cystic kidney disease +
cystitis +
detrusor sphincter dyssynergia
developmental and epileptic encephalopathy 116
diabetes insipidus +
dialysis-related amyloidosis
dicarboxylic aminoaciduria
dimethylglycine dehydrogenase deficiency
dioctophymiasis
diphthamide deficiency syndrome +
familial hypertryptophanemia
familial juvenile hyperuricemic nephropathy
female stress incontinence
fumarase deficiency
gamma-amino butyric acid metabolism disorder +
gamma-glutamyl transpeptidase deficiency
glutamate-cysteine ligase deficiency
glutathione synthetase deficiency +
glycine encephalopathy +
Goodpasture syndrome +
granulomatosis with polyangiitis
Hantavirus hemorrhagic fever with renal syndrome +
Hartnup disease
hawkinsinuria
hemolytic-uremic syndrome
histidine metabolism disease +
HMG-CoA synthase 2 deficiency
homocystinuria
homocystinuria-megaloblastic anemia cblE type
homocystinuria-megaloblastic anemia cblG type
hydroxykynureninuria
hyperhomocysteinemia
hyperlysinemia
hypermethioninemia +
hyperprolinemia +
hypervalinemia and hyperleucine-isoleucinemia
hypophosphatemic nephrolithiasis/osteoporosis +
immunoglobulin heavy chain amyloidosis
immunoglobulin light chain amyloidosis
kidney benign neoplasm +
kidney cancer +
kidney carcinoma in situ
kidney cortex disease +
kidney failure +
kidney hypertrophy
kidney papillary necrosis
leucine-sensitive hypoglycemia of infancy
low compliance bladder
lysinuric protein intolerance
mitochondrial short-chain enoyl-CoA hydratase 1 deficiency
multiple carboxylase deficiency +
nephritis +
nephrocalcinosis
nephrolithiasis +
nephronophthisis +
neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities
neurodevelopmental disorder with spastic paraplegia and microcephaly
neurogenic bladder
obstructive nephropathy
organic acidemia +
ornithine translocase deficiency
orthostatic proteinuria
overactive bladder syndrome
oxoglutarate dehydrogenase deficiency
pentosuria
perinephritis
phenylketonuria
prolidase deficiency
proteinuria +
pyelitis +
pyoureter
renal agenesis +
renal fibrosis
renal hypertension +
renal hypoplasia +
renal infectious disease
renal osteodystrophy
renal tuberculosis
renal tubular transport disease +
sarcosinemia
secondary hyperparathyroidism of renal origin
serine deficiency +
serum amyloid A amyloidosis
stricture or kinking of ureter
systemic primary carnitine deficiency disease
tetrahydrobiopterin (BH4)-deficient hyperphenylalaninemia +
tyrosinemia +
urea cycle disorder +
ureter cancer +
ureter tuberculosis
ureteral benign neoplasm +
ureteral obstruction
ureterocele
ureterolithiasis
urinary bladder cancer +
urinary schistosomiasis
vesicoureteral reflux