Disease #04347

Official abbreviation FAME-2;FMCTE-2
Name epilepsy, myoclonic, familial adult, type 2 (FAME-2)
OMIM ID 607876
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 2 genes ADRA2B, STARD7
Associated tissues -
Disease features -
Remarks -