Disease #03012

Official abbreviation EIG-13;EJM-5
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 0
Phenotype entries for this disease 0
Associated with 1 gene GABRA1
Associated tissues -
Disease features -
Remarks -