Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4014408
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 		0.400 Biomarker disease GENOMICS_ENGLAND Mutations in the UQCC1-interacting protein, UQCC2, cause human complex III deficiency associated with perturbed cytochrome b protein expression. 24385928 2013
CUI: C4014408
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 		0.400 Biomarker disease GENOMICS_ENGLAND Mutations in the UQCC1-interacting protein, UQCC2, cause human complex III deficiency associated with perturbed cytochrome b protein expression. 24385928 2013
CUI: C4014408
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 		0.400 Biomarker disease GENOMICS_ENGLAND Mutations in the UQCC1-interacting protein, UQCC2, cause human complex III deficiency associated with perturbed cytochrome b protein expression. 24385928 2013
CUI: C4014408
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 		0.400 CausalMutation disease CLINVAR