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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking FGB and Congenital Hypodysfibrinogenemia 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)
  • 3 RGD objects have been annotated to Congenital Hypodysfibrinogenemia  (DOID:9004929)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: FIBRINOGEN NIJMEGEN
  • Original References(s): PMID:1565641 PMID:25741868 PMID:31064749


    • An association has been curated linking FGB and Congenital Hypodysfibrinogenemia 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)
  • 3 RGD objects have been annotated to Congenital Hypodysfibrinogenemia  (DOID:9004929)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: FIBRINOGEN LONGMONT
  • Original References(s): PMID:11468164 PMID:25741868 PMID:31064749


    • An association has been curated linking FGB and Congenital Hypodysfibrinogenemia 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)
  • 3 RGD objects have been annotated to Congenital Hypodysfibrinogenemia  (DOID:9004929)
  • 28 papers in RGD have been used to annotate FGB
  • Curation Notes: ClinVar Annotator: match by term: FIBRINOGEN BALTIMORE 2
  • Original References(s): PMID:25741868 PMID:3194892


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