Disease: Optic Atrophies, Hereditary ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0029125
Disease: Optic Atrophies, Hereditary
Optic Atrophies, Hereditary 		0.300 Biomarker group CTD_human Mitochondrial genetic control of assembly and function of complex I in mammalian cells. 11695835 2001
CUI: C0029125
Disease: Optic Atrophies, Hereditary
Optic Atrophies, Hereditary 		0.300 Biomarker group CTD_human Respiration and growth defects in transmitochondrial cell lines carrying the 11778 mutation associated with Leber's hereditary optic neuropathy. 8662757 1996