Disease #02931 (ENFL4 (epilepsy, frontal lobe, nocturnal, type 4 (ENFL-4)), OMIM:610353)

Official abbreviation ENFL4
Name epilepsy, frontal lobe, nocturnal, type 4 (ENFL-4)
OMIM ID 610353
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 CHRNA2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00448782 230034 - - M no Germany - - - - - ENFL4 Delayed speech and language development, Episodic ataxia, Epileptic spasm, Infantile spasms CHRNA2 CHRNA2 1 1 Andreas Laner
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