Disease #01146 (ENFL5 (epilepsy, frontal lobe, nocturnal, type 5 (ENFL-5)), OMIM:615005)

Official abbreviation ENFL5
Name epilepsy, frontal lobe, nocturnal, type 5 (ENFL-5)
OMIM ID 615005
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene KCNT1
Associated tissues -
Disease features -
Remarks -