Disease table of MYOCLONIC EPILEPSY, FAMILIAL INFANTILE OMIM ID: 605021

Gene-disease associations table

Gene	Associated with MYOCLONIC EPILEPSY, FAMILIAL INFANTILE in	Link to HGNC	Cytogenetic band	Number of associated diseases	Associated diseases
TBC1D24	ClinVar, OMIM, HUMSAVAR	HGNC link	16p13.3	6	PS220290, 605021, PS124900, PS308350, PS254800, 220500