CYC1, cytochrome c1, 1537

N. diseases: 44; N. variants: 3
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3809553
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 		0.600 Biomarker disease GENOMICS_ENGLAND Mutations in CYC1, encoding cytochrome c1 subunit of respiratory chain complex III, cause insulin-responsive hyperglycemia. 23910460 2013
CUI: C3809553
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 		0.600 GeneticVariation disease UNIPROT Mutations in CYC1, encoding cytochrome c1 subunit of respiratory chain complex III, cause insulin-responsive hyperglycemia. 23910460 2013
CUI: C3809553
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 		0.600 Biomarker disease GENOMICS_ENGLAND
CUI: C3809553
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 		0.600 CausalMutation disease CLINVAR