Disease table of CONVULSIONS, FAMILIAL INFANTILE, WITH PAROXYSMAL CHOREOATHETOSIS OMIM ID: 602066

Gene-disease associations table

Gene	Associated with CONVULSIONS, FAMILIAL INFANTILE, WITH PAROXYSMAL CHOREOATHETOSIS in	Link to HGNC	Cytogenetic band	Number of associated diseases	Associated diseases
PRRT2	ClinVar, OMIM, HUMSAVAR	HGNC link	16p11.2	3	602066, PS128100, PS601764