4 entries on 1 page. Showing entries 1 - 4.

10 per page 25 per page 50 per page 100 per page 250 per page 500 per page 1000 per page

ID	Abbreviation	Name	OMIM ID	Individuals	Phenotypes	Associated with genes	Associated tissues	Disease features
00025	614053	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 3, 614053 (3)	614053	0	0	ATP5E, ATP5F1E	-	-
00010	615228	Mitochondrial complex (ATP synthase) deficiency, nuclear type 4, 615228 (3)	615228	0	0	ATP5A1, ATP5F1A	-	-
00502	616045	?Combined oxidative phosphorylation deficiency 22, 616045 (3)	616045	0	0	ATP5A1, ATP5F1A	-	-
00579	618120	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5; MC5DN5	618120	0	0	ATP5F1D	-	-

10 per page 25 per page 50 per page 100 per page 250 per page 500 per page 1000 per page