3 entries on 1 page. Showing entries 1 - 3.

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
00520	616794	Combined oxidative phosphorylation deficiency 28, 616794 (3)	616794	0	0	SLC25A26	-	-
00437	CACTD	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY;CACTD	212138	0	0	SLC25A20	-	-
00103	EIEE3	Epileptic encephalopathy, early infantile, 3, 609304 (3)	609304	0	0	SLC25A22	-	-

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