Disease table of MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1 OMIM ID: 604273

Gene-disease associations table

Gene	Associated with MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1 in	Link to HGNC	Cytogenetic band	Number of associated diseases	Associated diseases
ATPAF2	ClinVar, OMIM, HUMSAVAR	HGNC link	17p11.2	1	604273