Disease #02683

Official abbreviation EJA-1
Name epilepsy, juvenile absence, susceptibility to, type 1 (EJA-1)
OMIM ID 607631
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene EFHC1
Associated tissues -
Disease features -
Remarks -