Disease table of MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2 OMIM ID: 614052

Gene-disease associations table

Gene	Associated with MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2 in	Link to HGNC	Cytogenetic band	Number of associated diseases	Associated diseases
TMEM70	ClinVar, OMIM, HUMSAVAR	HGNC link	8q21.11	1	614052