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GENE - TERM ANNOTATION REPORT

46 Annotations Found.

An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40815755 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Mitochondrial complex IV deficiency
  • Original References(s): PMID:25741868


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred from experiment (EXP)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8563306 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Mitochondrial complex IV deficiency
  • Original References(s): PMID:15214016


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8563299 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:10443880 PMID:10636738 PMID:22488715 PMID:23829769 PMID:24027061 PMID:28492532 PMID:28639102 PMID:32445240 PMID:34302356 PMID:9837813 PMID:9843204


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8563302 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Mitochondrial complex IV deficiency
  • Original References(s): PMID:9837813


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8563295 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Mitochondrial complex IV deficiency
  • Original References(s): PMID:9843204


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8563301 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Mitochondrial complex IV deficiency
  • Original References(s): PMID:9837813


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8563303 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Mitochondrial complex IV deficiency
  • Original References(s): PMID:10647889


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8602053 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Mitochondrial complex IV deficiency
  • Original References(s): PMID:21937992


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10411018 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:12515039 PMID:12943968 PMID:16326995 PMID:16542579 PMID:19780766 PMID:23829769 PMID:24027061 PMID:25741868 PMID:27896082 PMID:28492532


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13445813 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151747873 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:10443880 PMID:22488715 PMID:24027061 PMID:25741868 PMID:28492532


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:329350147 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150546881 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Mitochondrial complex IV deficiency
  • Original References(s): PMID:25741868


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156434211 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156434222 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150528472 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10409682 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156434233 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151758490 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156434235 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10410883 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868 PMID:27756633 PMID:28492532


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156434232 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156434191 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156434190 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156434236 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156434237 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12849038 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:10443880 PMID:16199547 PMID:16542579 PMID:22488715 PMID:23829769 PMID:24027061 PMID:24462369 PMID:25741868 PMID:28492532


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8693112 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150334114 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12894916 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156434192 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156434193 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150337480 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8563305 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:10746561 PMID:20624914 PMID:28492532


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151236243 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:12515039 PMID:19780766 PMID:23829769 PMID:24027061 PMID:25741868 PMID:27896082 PMID:28492532 PMID:30872186


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12742194 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:17576681 PMID:22488715 PMID:23829769 PMID:25741868 PMID:28492532 PMID:32445240 PMID:9536098


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12893218 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:10443880 PMID:10746561 PMID:11317352 PMID:15214016 PMID:22488715 PMID:24027061 PMID:25111564 PMID:25741868 PMID:28492532 PMID:29933018


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10411499 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29933018


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401830883 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401855741 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156434200 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868 PMID:36675121


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13530239 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:10443880 PMID:25111564 PMID:27756633 PMID:28492532 PMID:33134083 PMID:9837813 PMID:9843204


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10410591 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:22488715 PMID:23829769 PMID:25741868 PMID:28492532 PMID:35693685


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14350394 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:16326995 PMID:17576681 PMID:18583168 PMID:22488715 PMID:23829769 PMID:25741868 PMID:28492532 PMID:29933018 PMID:9536098 PMID:9837813


  • An association has been curated linking SURF1 and cytochrome-c oxidase deficiency disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150475922 (Homo sapiens)
  • 352 RGD objects have been annotated to cytochrome-c oxidase deficiency disease  (DOID:3762)
  • 6 papers in RGD have been used to annotate SURF1
  • Curation Notes: ClinVar Annotator: match by term: Cytochrome-c oxidase deficiency disease
  • Original References(s): PMID:25741868 PMID:28492532 PMID:36675121


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