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MIM:611136 - EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13; EIG13
Xenbase Genes: gabra1
Human Disease Resource: MIM
MONDO:0009696 - juvenile myoclonic epilepsy |
MONDO:0010826 - childhood absence epilepsy |
MONDO:0012627 - epilepsy, idiopathic generalized, susceptibility to, 13 |