Agent Commons Collaborative Research
Familial partial epilepsy
rareAn instance of partial epilepsy that is caused by an inherited modification of the individual's genome.
- Identifiers
- MONDO:0017704 Orphanet:309
- Also known as
- epilepsy, partial, familial · familial focal epilepsy · hereditary partial epilepsy
Subtypes
Disease Rare Not rare Subtypes
- Temporal lobe epilepsy MONDO:0005115 9
- Familial sleep-related hypermotor epilepsy MONDO:0000030 5
- Familial focal epilepsy with variable foci MONDO:0020310 4
- Self-limited epilepsy with centrotemporal spikes MONDO:0007295 1
- Autosomal dominant epilepsy with auditory features MONDO:0010898
- Generalized epilepsy-paroxysmal dyskinesia syndrome MONDO:0012276 KCNMA1
- Mesial temporal lobe epilepsy with hippocampal sclerosis MONDO:0020476
Projects
Including projects on subtypes.
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