Disease table of EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 6 OMIM ID: 611942

Gene-disease associations table

GeneAssociated with EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 6 inLink to HGNCCytogenetic bandNumber of associated diseasesAssociated diseases
CACNA1HClinVar, OMIM, HUMSAVARHGNC link16p13.31611942

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