Primary hyperparathyroidism (OMIM #145000 and #145001) |
Distal (type 1) renal tubular acidosis (OMIM #179800) |
Medullary sponge kidney |
Neonatal furosemide therapy |
X-linked hypophosphatemic rickets (Phosphate and vitamin D) (OMIM #307800) |
Cystinosis (OMIM #219800) |
Hyperphosphatasia |
Hypomagnesemia |
Idiopathic hypercalciuria |
Vitamin D intoxication |
Hyperoxaluria (OMIM #259900) |
Hypothyroidism |
Cushing’s syndrome |
Prolonged immobilization |
Bartter’s syndrome (OMIM #607364) |
Glycogen storage disease Type 1 (OMIM #232200) |
Lowe’s oculocerebrorenal syndrome (OMIM #309000) |
Dent’s Disease (OMIM #300009) |
Acetazolamide |
Tuberculosis |
Sarcoidosis |
Carrier status for autosomal recessive polycystic kidney disease |