Disease: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4225206
Disease: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28 		0.700 GeneticVariation disease UNIPROT Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26. 26522469 2015
CUI: C4225206
Disease: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28 		0.700 GermlineCausalMutation disease ORPHANET Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26. 26522469 2015
CUI: C4225206
Disease: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28 		0.700 Biomarker disease GENOMICS_ENGLAND Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26. 26522469 2015
CUI: C4225206
Disease: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28 		0.700 Biomarker disease CTD_human
CUI: C4225206
Disease: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28 		0.700 CausalMutation disease CLINVAR