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GENE - TERM ANNOTATION REPORT

41 Annotations Found.

An association has been curated linking Aldob and hereditary fructose intolerance syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Brooks CC and Tolan DR, Am J Hum Genet 1993 Apr;52(4):835-40.
  • The annotation has been inferred from sequence orthology with ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Brooks CC and Tolan DR, Am J Hum Genet 1993 Apr;52(4):835-40.
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Esposito G, etal., Hum Mutat. 2004 Dec;24(6):534.
  • The annotation has been inferred from sequence orthology with ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Esposito G, etal., Hum Mutat. 2004 Dec;24(6):534.
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Qualifier: susceptibility


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by OMIM:229600
  • Original References(s): PMID:8071980


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Hereditary fructose intolerance
  • Original References(s): PMID:28492532


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by OMIM:229600
  • Original References(s): PMID:15532022, PMID:20848650


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by OMIM:229600
  • Original References(s): PMID:25595217


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by OMIM:229600
  • Original References(s): PMID:2203259


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by OMIM:229600
  • Original References(s): PMID:10352930


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by OMIM:229600
  • Original References(s): PMID:20848650


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by OMIM:229600
  • Original References(s): PMID:1967768


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by OMIM:229600
  • Original References(s): PMID:7717389


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by OMIM:229600
  • Original References(s): PMID:18541450


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with ALDOB (Homo sapiens) [(EXP) inferred from experiment]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:3383242, PMID:15733923, PMID:18035330


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by OMIM:229600


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Fructose-1,6-bisphosphate aldolase B deficiency
  • Original References(s): PMID:11757579, PMID:12205126, PMID:12417303, PMID:12464284, PMID:15532022, PMID:15733923, PMID:15880727, PMID:16406649, PMID:18541450, PMID:1967768, PMID:19768653, PMID:20033295, PMID:23114028, PMID:23430936, PMID:24033266, PMID:25741868, PMID:2623136, PMID:26677512, PMID:26937407, PMID:27797444, PMID:28492532, PMID:3383242, PMID:6348085, PMID:8096362


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Fructose intolerance
  • Original References(s): PMID:20848650, PMID:22494545, PMID:23430936, PMID:28492532


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Fructose-1,6-bisphosphate aldolase B deficiency
  • Original References(s): PMID:18541450, PMID:28492532


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Fructose-1,6-bisphosphate aldolase B deficiency
  • Original References(s): PMID:18541450, PMID:25595217, PMID:28492532


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Fructose-1,6-bisphosphate aldolase B deficiency
  • Original References(s): PMID:15880727, PMID:16406649, PMID:16630753, PMID:20848650, PMID:23114028, PMID:28492532, PMID:8438046


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Fructose-1,6-bisphosphate aldolase B deficiency
  • Original References(s): PMID:10024431, PMID:10229688, PMID:15532022, PMID:18541450, PMID:20848650, PMID:25595217, PMID:25741868, PMID:28492532, PMID:32860008, PMID:9610797


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Fructose-1,6-bisphosphate aldolase B deficiency
  • Original References(s): PMID:10625657, PMID:11757579, PMID:12205126, PMID:12417303, PMID:15880727, PMID:18541450, PMID:1967768, PMID:20033295, PMID:23430936, PMID:25741868, PMID:26937407, PMID:28492532, PMID:32860008


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Fructose-1,6-bisphosphate aldolase B deficiency
  • Original References(s): PMID:15880727, PMID:2349937, PMID:25741868, PMID:28492532


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Fructose-1,6-bisphosphate aldolase B deficiency
  • Original References(s): PMID:11757579, PMID:12205126, PMID:12417303, PMID:15880727, PMID:18541450, PMID:1856829, PMID:19768653, PMID:20033295, PMID:20882353, PMID:2336380, PMID:23430936, PMID:28492532, PMID:30311386, PMID:8541450


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Hereditary fructose intolerance
  • Original References(s): PMID:15532022


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Hereditary fructose intolerance
  • Original References(s): PMID:16406649


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Hereditary fructose intolerance
  • Original References(s): PMID:23430936


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Fructose-1,6-bisphosphate aldolase B deficiency
  • Original References(s): PMID:15880727, PMID:18541450, PMID:20033295, PMID:20882353, PMID:25741868, PMID:26937407, PMID:28492532, PMID:8071980, PMID:8299883, PMID:8299892


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Fructose-1,6-bisphosphate aldolase B deficiency
  • Original References(s): PMID:10024431, PMID:11757579, PMID:20033295, PMID:20848650, PMID:28492532, PMID:8071980, PMID:8535439, PMID:9610797


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Hereditary fructose intolerance
  • Original References(s): PMID:26633542, PMID:28492532


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Fructose intolerance
  • Original References(s): PMID:15880727, PMID:18541450, PMID:28492532


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Hereditary fructose intolerance
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Hereditary fructose intolerance
  • Original References(s): PMID:25741868


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Hereditary fructose intolerance
  • Original References(s): PMID:15880727, PMID:16406649, PMID:23430936


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Fructose intolerance
  • Original References(s): PMID:28492532, PMID:8438046


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Hereditary fructose intolerance
  • Original References(s): PMID:15532022, PMID:20848650, PMID:23430936


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Hereditary fructose intolerance
  • Original References(s): PMID:20882353, PMID:28492532


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Fructose-1,6-bisphosphate aldolase B deficiency
  • Original References(s): PMID:10970798, PMID:20848650, PMID:21228398, PMID:22995991


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Fructose intolerance
  • Original References(s): PMID:16406649, PMID:20848650


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Fructose-1,6-bisphosphate aldolase B deficiency
  • Original References(s): PMID:12205126, PMID:15532022, PMID:18541450, PMID:20848650, PMID:25525159, PMID:28492532


  • An association has been curated linking Aldob and hereditary fructose intolerance syndrome 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 ALDOB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 CRRD objects have been annotated to hereditary fructose intolerance syndrome  (DOID:9869)
  • 46 papers in CRRD have been used to annotate Aldob
  • Curation Notes: ClinVar Annotator: match by term: Fructose-1,6-bisphosphate aldolase B deficiency
  • Original References(s): PMID:15880727, PMID:1967768, PMID:20848650, PMID:28492532, PMID:31591370


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.