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GENE - TERM ANNOTATION REPORT

49 Annotations Found.

An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric acidemia IIC
  • Original References(s): PMID:12815589 PMID:7173259 PMID:7173260


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:25741868


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Multiple acyl-CoA dehydrogenase deficiency
  • Original References(s): PMID:19758981 PMID:23628458 PMID:24357026 PMID:24522293 PMID:25913573 PMID:28492532 PMID:29336361


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric acidemia IIC


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric acidemia IIC
  • Original References(s): PMID:19249206


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:21907580 PMID:23628458 PMID:24522293


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:17977044 PMID:28492532 PMID:28914566


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Multiple acyl-CoA dehydrogenase deficiency
  • Original References(s): PMID:19758981 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:28492532 PMID:30587156


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:17584774 PMID:23727839 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:24190796 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:18289905 PMID:19758981 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:12359134 PMID:20138856 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric acidemia iic, late-onset
  • Original References(s): PMID:16434667 PMID:17412732


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:19249206 PMID:20370797 PMID:21347544 PMID:22013910 PMID:24357026 PMID:25741868 PMID:27000805 PMID:27270537 PMID:27935074 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Multiple acyl-CoA dehydrogenase deficiency
  • Original References(s): PMID:12359134 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:27000805 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:25827849 PMID:28492532 PMID:29988809 PMID:30022752


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:16510302 PMID:23785301 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:12359134 PMID:12815589 PMID:17584774 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Multiple acyl-CoA dehydrogenase deficiency
  • Original References(s): PMID:12359134 PMID:15669683 PMID:22611163 PMID:25741868 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Multiple acyl-CoA dehydrogenase deficiency
  • Original References(s): PMID:19758981 PMID:21347544 PMID:23628458 PMID:24357026 PMID:24522293 PMID:27038534 PMID:28492532 PMID:29336361


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:19758981 PMID:24357026 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Multiple acyl-CoA dehydrogenase deficiency
  • Original References(s): PMID:23628458 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:24516753 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Multiple acyl-CoA dehydrogenase deficiency
  • Original References(s): PMID:12359134 PMID:17584774 PMID:22611163 PMID:25741868 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:12359134 PMID:24190796 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Multiple acyl-CoA dehydrogenase deficiency
  • Original References(s): PMID:17412732 PMID:17584774 PMID:22611163 PMID:24190796 PMID:25741868 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Multiple acyl-CoA dehydrogenase deficiency
  • Original References(s): PMID:18289905 PMID:20138856 PMID:20370797 PMID:21347544 PMID:23628458 PMID:28492532 PMID:29988809


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Multiple acyl-CoA dehydrogenase deficiency
  • Original References(s): PMID:12359134 PMID:16527485 PMID:17412732 PMID:17584774 PMID:22611163 PMID:23727839 PMID:25741868 PMID:26403312 PMID:27038534 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Multiple acyl-CoA dehydrogenase deficiency
  • Original References(s): PMID:24357026 PMID:27060313 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:19758981 PMID:21347544 PMID:23628458 PMID:24357026 PMID:24522293 PMID:28492532 PMID:29336361


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Multiple acyl-CoA dehydrogenase deficiency
  • Original References(s): PMID:17977044


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:22041377 PMID:24522293 PMID:25827849 PMID:28492532 PMID:29336361


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:18289905 PMID:21088898 PMID:22664151 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:18289905 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Glutaric aciduria, type 2
  • Original References(s): PMID:12815589 PMID:24516753 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Multiple acyl-CoA dehydrogenase deficiency
  • Original References(s): PMID:27038534


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Multiple acyl-CoA dehydrogenase deficiency
  • Original References(s): PMID:20138856 PMID:22664151 PMID:28492532


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Multiple acyl-CoA dehydrogenase deficiency
  • Original References(s): PMID:15669683 PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Multiple acyl-CoA dehydrogenase deficiency
  • Original References(s): PMID:20023066 PMID:27038534 PMID:28492532 PMID:31268564


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Multiple acyl-CoA dehydrogenase deficiency
  • Original References(s): PMID:19265687 PMID:19758981 PMID:28492532 PMID:32393189


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Multiple acyl-CoA dehydrogenase deficiency
  • Original References(s): PMID:12815589 PMID:25741868 PMID:28492532 PMID:31268564


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Multiple acyl-CoA dehydrogenase deficiency
  • Original References(s): PMID:24357026 PMID:28492532 PMID:29336361


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Multiple acyl-CoA dehydrogenase deficiency
  • Original References(s): PMID:17576681 PMID:28492532 PMID:7757062 PMID:9536098


  • An association has been curated linking Etfdh and multiple acyl-CoA dehydrogenase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with ETFDH (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to multiple acyl-CoA dehydrogenase deficiency  (DOID:0060358)
  • 12 papers in RGD have been used to annotate Etfdh
  • Curation Notes: ClinVar Annotator: match by term: Multiple acyl-CoA dehydrogenase deficiency
  • Original References(s): PMID:15669683 PMID:25741868


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