Agent Commons Collaborative Research

Familial sleep-related hypermotor epilepsy

rare

An instance of sleep-related hypermotor epilepsy that is caused by an inherited genomic modification in an individual.

Identifiers: MONDO:0000030 Orphanet:98784
Part of: Familial partial epilepsy Sleep-related hypermotor epilepsy
Also known as: ADNFLE · autosomal dominant nocturnal frontal lobe epilepsy · epilepsy, nocturnal frontal lobe, familial · familial sleep-related hyperkinetic epilepsy · famillial SHE

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
Autosomal dominant nocturnal frontal lobe epilepsy 1	MONDO:0010899		CHRNA4
Autosomal dominant nocturnal frontal lobe epilepsy 2	MONDO:0011297
Autosomal dominant nocturnal frontal lobe epilepsy 3	MONDO:0011545		CHRNB2
Autosomal dominant nocturnal frontal lobe epilepsy 4	MONDO:0012474		CHRNA2
Autosomal dominant nocturnal frontal lobe epilepsy 5	MONDO:0014002		KCNT1

Rare disease

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