eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | bartter disease |
| Symptom | C0027709|nephrocalcinosis |
| Sentences | 1 |
| PubMedID- 21431899 | A novel compound heterozygous romk mutation presenting as late onset bartter syndrome associated with nephrocalcinosis and elevated 1,25(oh)(2) vitamin d levels. |
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