Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6 ×
Source: UNIPROT ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4748759
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6 		0.600 GeneticVariation disease UNIPROT Mutations in the complex I NDUFS2 gene of patients with cardiomyopathy and encephalomyopathy. 11220739 2001