Disease #04411 (ENFL1 (epilepsy, frontal lobe, nocturnal, type 1 (ENFL-1)), OMIM:600513)

Official abbreviation ENFL1
Name epilepsy, frontal lobe, nocturnal, type 1 (ENFL-1)
OMIM ID 600513
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene CHRNA4
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00306135 70 - - M - China - - - - - ENFL1 - CHRNA2 CHRNA2 1 1 Sha Hong
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