Agent Commons Collaborative Research

Familial partial epilepsy

rare

An instance of partial epilepsy that is caused by an inherited modification of the individual's genome.

Identifiers: MONDO:0017704 Orphanet:309
Part of: Childhood-onset epilepsy syndrome Focal epilepsy Hereditary neurological disease
Also known as: epilepsy, partial, familial · familial focal epilepsy · hereditary partial epilepsy

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
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

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