Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 374291
Gene Symbol: NDUFS7
NDUFS7
CUI: C4748752
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3 		0.600 GeneticVariation UNIPROT Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex I. 10360771

1999
Entrez Id: 374291
Gene Symbol: NDUFS7
NDUFS7
CUI: C4748752
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3 		0.600 GeneticVariation UNIPROT Human mitochondrial complex I in health and disease. 10330338

1999