eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | autosomal dominant hypocalcemia |
| Comorbidity | C0004775|bartter syndrome |
| Sentences | 1 |
| PubMedID- 25932037 | This study presents a patient who had autosomal dominant hypocalcemia with bartter syndrome due to an activating mutation y829c in the transmembrane domain of the casr. |
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