Disease table of EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5 OMIM ID: 612269

Gene-disease associations table

GeneAssociated with EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5 inLink to HGNCCytogenetic bandNumber of associated diseasesAssociated diseases
GABRB3ClinVar, OMIM, HUMSAVARHGNC link15q121612269

Download the disease annotation in CSV format