2 entries on 1 page. Showing entries 1 - 2.

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
00510	617069	?Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3, 617069 (3)	617069	0	0	TK2	-	-
00030	MTDPS2	Mitochondrial DNA depletion syndrome 2 (myopathic type), 609560 (3)	609560	0	0	TK2	-	-

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