Disease: Unspecified visual loss ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3665346
Disease: Unspecified visual loss
Unspecified visual loss 		0.110 GeneticVariation phenotype BEFREE In particular, these mitochondrial haplogroup specific variants: m.3394T>C (MT-ND1), m.14502T>C (MT-ND4) and m.14693A>G (MT-TE) enhanced the penetrance of visual loss in these Chinese families. 23665487 2013
CUI: C3665346
Disease: Unspecified visual loss
Unspecified visual loss 		0.110 Biomarker phenotype HPO