PedAM
Pediatric Disease Annotations & Medicines
| Disease | hypocalcemia |
| Phenotype | C0026848|myopathy |
| Sentences | 2 |
| PubMedID- 25227914 | Dominant mutations in orai1 cause tubular aggregate myopathy with hypocalcemia via constitutive activation of store-operated ca(2)(+) channels. |
| PubMedID- 21886637 | An overt myopathy due to hypocalcemia rarely occurs. |
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