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ID	Abbreviation	Name	OMIM ID	Individuals	Phenotypes	Associated with genes	Associated tissues	Disease features
00037	612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy), 612075 (3)	612075	0	0	RRM2B	-	-
00049	PEOA5	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 5, PEOA5	613077	0	0	RRM2B	-	-

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