Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 29078
Gene Symbol: NDUFAF4
NDUFAF4
CUI: C4748778
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15 		0.600 GeneticVariation UNIPROT NDUFAF4 variants are associated with Leigh syndrome and cause a specific mitochondrial complex I assembly defect. 28853723

2017
Entrez Id: 29078
Gene Symbol: NDUFAF4
NDUFAF4
CUI: C4748778
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15 		0.600 GeneticVariation UNIPROT C6ORF66 is an assembly factor of mitochondrial complex I. 18179882

2008