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ID	Abbreviation	Name	OMIM ID	Individuals	Phenotypes	Associated with genes	Associated tissues	Disease features
00514	615578	Combined oxidative phosphorylation deficiency 18, 615578 (3)	615578	0	0	SFXN4	-	-
00491	FRDA;FRDA1;FA	FRIEDREICH ATAXIA 1; FRDA;FRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED	229300	0	0	FXN	-	-

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