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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking FTL and Glycogen Storage Disease 0, Muscle 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:9589330 (Homo sapiens)
  • 6 RGD objects have been annotated to Glycogen Storage Disease 0, Muscle  (DOID:9005648)
  • 18 papers in RGD have been used to annotate FTL
  • Curation Notes: ClinVar Annotator: match by term: Glycogen storage disease 0, muscle
  • Original References(s): PMID:17182944 PMID:18414213 PMID:25741868 PMID:28492532


    • An association has been curated linking FTL and Glycogen Storage Disease 0, Muscle 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:11665283|RGD:11665356|RGD:11665536|RGD:11665602|RGD:11665711|RGD:11665859|RGD:11665952|RGD:11666041|RGD:11666515 (Homo sapiens) & RGD:11665283|RGD:11665356|RGD:11665536|RGD:11665602|RGD:11665711|RGD:11665859|RGD:11665952|RGD:11666041|RGD:11666515 (Homo sapiens) & RGD:11665283|RGD:11665356|RGD:11665536|RGD:11665602|RGD:11665711|RGD:11665859|RGD:11665952|RGD:11666041|RGD:11666515 (Homo sapiens) & RGD:11665283|RGD:11665356|RGD:11665536|RGD:11665602|RGD:11665711|RGD:11665859|RGD:11665952|RGD:11666041|RGD:11666515 (Homo sapiens) & RGD:11665283|RGD:11665356|RGD:11665536|RGD:11665602|RGD:11665711|RGD:11665859|RGD:11665952|RGD:11666041|RGD:11666515 (Homo sapiens) & RGD:11665283|RGD:11665356|RGD:11665536|RGD:11665602|RGD:11665711|RGD:11665859|RGD:11665952|RGD:11666041|RGD:11666515 (Homo sapiens) & RGD:11665283|RGD:11665356|RGD:11665536|RGD:11665602|RGD:11665711|RGD:11665859|RGD:11665952|RGD:11666041|RGD:11666515 (Homo sapiens) & RGD:11665283|RGD:11665356|RGD:11665536|RGD:11665602|RGD:11665711|RGD:11665859|RGD:11665952|RGD:11666041|RGD:11666515 (Homo sapiens) & RGD:11665283|RGD:11665356|RGD:11665536|RGD:11665602|RGD:11665711|RGD:11665859|RGD:11665952|RGD:11666041|RGD:11666515 (Homo sapiens)
  • 6 RGD objects have been annotated to Glycogen Storage Disease 0, Muscle  (DOID:9005648)
  • 18 papers in RGD have been used to annotate FTL
  • Curation Notes: ClinVar Annotator: match by term: Glycogen storage disease 0, muscle


    • An association has been curated linking FTL and Glycogen Storage Disease 0, Muscle 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:11665316|RGD:11665389|RGD:11665548|RGD:11665571|RGD:11665804 (Homo sapiens) & RGD:11665316|RGD:11665389|RGD:11665548|RGD:11665571|RGD:11665804 (Homo sapiens) & RGD:11665316|RGD:11665389|RGD:11665548|RGD:11665571|RGD:11665804 (Homo sapiens) & RGD:11665316|RGD:11665389|RGD:11665548|RGD:11665571|RGD:11665804 (Homo sapiens) & RGD:11665316|RGD:11665389|RGD:11665548|RGD:11665571|RGD:11665804 (Homo sapiens)
  • 6 RGD objects have been annotated to Glycogen Storage Disease 0, Muscle  (DOID:9005648)
  • 18 papers in RGD have been used to annotate FTL
  • Curation Notes: ClinVar Annotator: match by term: Glycogen storage disease 0, muscle | ClinVar Annotator: match by term: Muscle glycogen synthase deficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking FTL and Glycogen Storage Disease 0, Muscle 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:11666158|RGD:11666245 (Homo sapiens) & RGD:11666158|RGD:11666245 (Homo sapiens)
  • 6 RGD objects have been annotated to Glycogen Storage Disease 0, Muscle  (DOID:9005648)
  • 18 papers in RGD have been used to annotate FTL
  • Curation Notes: ClinVar Annotator: match by term: Glycogen storage disease 0, muscle
  • Original References(s): PMID:25741868


    • An association has been curated linking FTL and Glycogen Storage Disease 0, Muscle 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:11665741|RGD:11666196 (Homo sapiens) & RGD:11665741|RGD:11666196 (Homo sapiens)
  • 6 RGD objects have been annotated to Glycogen Storage Disease 0, Muscle  (DOID:9005648)
  • 18 papers in RGD have been used to annotate FTL
  • Curation Notes: ClinVar Annotator: match by term: Glycogen storage disease 0, muscle
  • Original References(s): PMID:25741868 PMID:28492532


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