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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H02216 | Juvenile absence epilepsy | Juvenile absence epilepsy (JAE/EJA) is classified among the age-related idiopathic generalized epilepsies in adolescence. JAE is characterized by typical absence seizures, and a long-life prevalence of ... | Nervous system disease |
(EJA1) EFHC1 [HSA:114327] [KO:K23029] (EJA2) CLCN2 [HSA:1181] [KO:K05011] |
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| H02217 | Juvenile myoclonic epilepsy | Juvenile myoclonic epilepsy (JME/EJM) is the most common form of idiopathic generalized epilepsy. JME appears around puberty and is characterized by seizures with bilateral and irregular myoclonic jerks ... | Nervous system disease |
(EJM1) EFHC1 [HSA:114327] [KO:K23029] (EJM5) GABRA1 [HSA:2554] [KO:K05175] (EJM6) CACNB4 [HSA:785] [KO:K04865] (EJM7) GABRD [HSA:2563] [KO:K05184] (EJM8) CLCN2 [HSA:1181] [KO:K05011] (EJM10) ICK [HSA:22858] [KO:K08828] |
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