Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9997
Gene Symbol: SCO2
SCO2
0.120 GeneticVariation phenotype BEFREE Infants with deficiency of cytochrome c oxidase (COX) due to SCO2 mutations observed so far usually demonstrated early cardiomyopathy, encephalopathy and lactic acidosis. 19879173 2010
Entrez Id: 9997
Gene Symbol: SCO2
SCO2
0.120 GeneticVariation phenotype BEFREE Progressive cardiomyopathy, neuropathy and lactic acidosis are presented by infants with SCO2 gene mutations. 19353431 2009
Entrez Id: 9997
Gene Symbol: SCO2
SCO2
0.120 Biomarker phenotype HPO