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MIM:607682 - EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 9; EIG9
Xenbase Genes: clcn2, cacnb4
Human Disease Resource: MIM
| MONDO:0009696 - juvenile myoclonic epilepsy |
| MONDO:0011892 - anterior uvea |
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| MONDO:0009696 - juvenile myoclonic epilepsy |
| MONDO:0011892 - anterior uvea |