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GENE - TERM ANNOTATION REPORT

7 Annotations Found.

An association has been curated linking FGB and Hypofibrinogenemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for human HPO-to-gene-to-disease annotations
  • 39 RGD objects have been annotated to Hypofibrinogenemia  (HP:0011900)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: OMIM:202400


  • An association has been curated linking FGB and Hypofibrinogenemia 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.
  • 39 RGD objects have been annotated to Hypofibrinogenemia  (HP:0011900)
  • 28 papers in RGD have been used to annotate FGB


  • An association has been curated linking FGB and Hypofibrinogenemia 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)
  • 39 RGD objects have been annotated to Hypofibrinogenemia  (HP:0011900)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: Hypofibrinogenemia
  • Original References(s): PMID:12161363 PMID:15070683 PMID:25741868 PMID:31064749


  • An association has been curated linking FGB and Hypofibrinogenemia 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)
  • 39 RGD objects have been annotated to Hypofibrinogenemia  (HP:0011900)
  • 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 Hypofibrinogenemia 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)
  • 39 RGD objects have been annotated to Hypofibrinogenemia  (HP:0011900)
  • 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 Hypofibrinogenemia 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)
  • 39 RGD objects have been annotated to Hypofibrinogenemia  (HP:0011900)
  • 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 Hypofibrinogenemia 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)
  • 39 RGD objects have been annotated to Hypofibrinogenemia  (HP:0011900)
  • 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


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