Disease #04347

Official abbreviation FAME2;FMCTE2
Name epilepsy, myoclonic, familial adult, type 2 (FAME2)
OMIM ID 607876
Human Phenotype Ontology Project (HPO) HPO
Inheritance AD
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene STARD7
Associated tissues -
Disease features -
Remarks -