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GENE - TERM ANNOTATION REPORT

94 Annotations Found.

An association has been curated linking FGB and congenital afibrinogenemia 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:13531858 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Hypofibrinogenemia
  • Original References(s): PMID:10688828 PMID:19420351 PMID:24033266 PMID:25741868 PMID:28492532 PMID:31064749


  • An association has been curated linking FGB and congenital afibrinogenemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Spena S, etal., Blood 2002 Dec 15;100(13):4478-84. Epub 2002 Aug 1.
  • 3 additional annotations were made from Spena S, etal., Blood 2002 Dec 15;100(13):4478-84. Epub 2002 Aug 1.
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11598301 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11597647 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11547554 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital
  • Original References(s): PMID:25741868


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11595500 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11589503 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11652853 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11651927 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11584719 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11595221 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11586488 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11591926 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11645003 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11655884 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11590383 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:8565582 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital
  • Original References(s): PMID:10666208


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11591844 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11596147 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11590713 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:8565584 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital
  • Original References(s): PMID:12393540


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11658422 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11592803 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11597036 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:8565585 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital
  • Original References(s): PMID:12393540


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11660177 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11657938 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11551545 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital
  • Original References(s): PMID:25741868


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11586970 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11583699 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11660141 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11593889 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11664467 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11595840 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11585747 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11589886 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11587860 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11582608 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11597805 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11594103 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:8565581 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital
  • Original References(s): PMID:10666208


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11584192 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11598227 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11588968 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:8565587 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital
  • Original References(s): PMID:15070683


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11664376 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11547699 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital
  • Original References(s): PMID:25741868


  • An association has been curated linking FGB and congenital afibrinogenemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB


  • An association has been curated linking FGB and congenital afibrinogenemia 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:14975754 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Hypofibrinogenemia
  • Original References(s): PMID:25741868 PMID:31064749


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11584658 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital
  • Original References(s): PMID:28492532


  • An association has been curated linking FGB and congenital afibrinogenemia 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:8565588 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Hypofibrinogenemia, congenital
  • Original References(s): PMID:12161363 PMID:15070683 PMID:25741868 PMID:31064749


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11595193 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital
  • Original References(s): PMID:28492532


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11544106 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FGB and congenital afibrinogenemia 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:15174254 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital
  • Original References(s): PMID:27164460


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11585616 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital
  • Original References(s): PMID:28492532


  • An association has been curated linking FGB and congenital afibrinogenemia 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:8565575 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Hypofibrinogenemia
  • Original References(s): PMID:1565641 PMID:25741868 PMID:31064749


  • An association has been curated linking FGB and congenital afibrinogenemia 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:8565583 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Hypofibrinogenemia
  • Original References(s): PMID:11468164 PMID:25741868 PMID:31064749


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28874396 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28874814 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28870354 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital
  • Original References(s): PMID:21713329


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28870577 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28874402 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28877228 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28882125 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28876829 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28874589 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:8565577 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital
  • Original References(s): PMID:25741868 PMID:3194892


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28876833 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28877224 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28877235 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28882119 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28881765 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28877220 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28870581 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28877561 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28882116 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:11551148 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28874808 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28874398 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28874393 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28874400 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:15123943 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital
  • Original References(s): PMID:25592583 PMID:28492532


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28874810 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28874593 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28881751 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28874596 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28881760 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28870574 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28882129 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital
  • Original References(s): PMID:22273812


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28874591 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital


  • An association has been curated linking FGB and congenital afibrinogenemia 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:127288443 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Congenital afibrinogenemia
  • Original References(s): PMID:22836883 PMID:25741868 PMID:30349899 PMID:34355501


  • An association has been curated linking FGB and congenital afibrinogenemia 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:14975897 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Congenital afibrinogenemia
  • Original References(s): PMID:12573244 PMID:15795540 PMID:25741868 PMID:28492532 PMID:31064749


  • An association has been curated linking FGB and congenital afibrinogenemia 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:152157013 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Congenital afibrinogenemia
  • Original References(s): PMID:25741868 PMID:34355501


  • An association has been curated linking FGB and congenital afibrinogenemia 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:28881755 (Homo sapiens)
  • 6 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Congenital afibrinogenemia
  • Original References(s): PMID:25741868


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