Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3665346
Disease: Unspecified visual loss
Unspecified visual loss
0.130 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
0.130 GeneticVariation phenotype BEFREE Mutant NADH dehydrogenase subunit 4 gene delivery to mitochondria by targeting sequence-modified adeno-associated virus induces visual loss and optic atrophy in mice. 22773905 2012
CUI: C3665346
Disease: Unspecified visual loss
Unspecified visual loss
0.130 GeneticVariation phenotype BEFREE Of other variants, the homoplasmic G11696A mutation in the ND4 gene is of special interest as it was implicated to be associated with LHON in a large Dutch family and five Chinese pedigrees with extremely penetrance of visual loss. 17300996 2007
CUI: C3665346
Disease: Unspecified visual loss
Unspecified visual loss
0.130 Biomarker phenotype HPO