Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4705
Gene Symbol: NDUFA10
NDUFA10
CUI: C4748796
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 22
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 22 		0.600 GeneticVariation UNIPROT A Comprehensive Genomic Analysis Reveals the Genetic Landscape of Mitochondrial Respiratory Chain Complex Deficiencies. 26741492

2016
Entrez Id: 4705
Gene Symbol: NDUFA10
NDUFA10
CUI: C4748796
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 22
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 22 		0.600 GeneticVariation UNIPROT NDUFA10 mutations cause complex I deficiency in a patient with Leigh disease. 21150889

2011