PedAM
Pediatric Disease Annotations & Medicines
| Disease | dent disease |
| Phenotype | C0027709|nephrocalcinosis |
| Sentences | 1 |
| PubMedID- 23334384 | Adenine phosphoribosyltransferase (aprt) deficiency, cystinuria, dent disease, familial hypomagnesemia with hypercalciuria and nephrocalcinosis (fhhnc), and primary hyperoxaluria (ph) are rare but important causes of severe kidney stone disease and/or chronic kidney disease in children. |
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