eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | dravet syndrome |
| Symptom | C0543888|epileptic encephalopathy |
| Sentences | 1 |
| PubMedID- 24207121 | De novo loss-of-function mutations in chd2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with dravet syndrome. |
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