Disease #03928 (FAME5 (epilepsy, myoclonic, familial adult, type 5 (FAME5)), OMIM:615400)

Official abbreviation FAME5
Name epilepsy, myoclonic, familial adult, type 5 (FAME5)
OMIM ID 615400
Human Phenotype Ontology Project (HPO) HPO
Inheritance AR
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CNTN2
Associated tissues -
Disease features -
Remarks -