Disease #03012 (EIG13;EJM5 (epilepsy, idiopathic, generalized, susceptibility to, type 13 (EIG-13, epilepsy, myoclonic, juvenile, type 5 (EJM-5))), OMIM:611136)

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Official abbreviation	EIG13;EJM5
Name	epilepsy, idiopathic, generalized, susceptibility to, type 13 (EIG-13, epilepsy, myoclonic, juvenile, type 5 (EJM-5))
OMIM ID	611136
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GABRA1
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)

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