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

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ID	Abbreviation	Name	OMIM ID	Individuals	Phenotypes	Associated with genes	Associated tissues	Disease features
00565	617950	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 36	617950	0	0	MRPS2	-	-
00099	COXPD5	Combined oxidative phosphorylation deficiency 5, 611719 (3)	611719	0	0	MRPS22	-	-

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