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

Gene-disease associations table

Gene	Associated with EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 6 in	Link to HGNC	Cytogenetic band	Number of associated diseases	Associated diseases
CACNA1H	ClinVar, OMIM, HUMSAVAR	HGNC link	16p13.3	1	611942