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GENE - TERM ANNOTATION REPORT

17 Annotations Found.

An association has been curated linking MYH7 and Scapuloperoneal myopathy 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:11645551 (Homo sapiens)
  • 5 RGD objects have been annotated to Scapuloperoneal myopathy  (HP:0009054)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Scapuloperoneal myopathy
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYH7 and Scapuloperoneal myopathy 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:11645719 (Homo sapiens)
  • 5 RGD objects have been annotated to Scapuloperoneal myopathy  (HP:0009054)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Scapuloperoneal myopathy


  • An association has been curated linking MYH7 and Scapuloperoneal myopathy 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:8605775 (Homo sapiens)
  • 5 RGD objects have been annotated to Scapuloperoneal myopathy  (HP:0009054)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Scapuloperoneal myopathy
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532 PMID:29300372


  • An association has been curated linking MYH7 and Scapuloperoneal myopathy 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:10046372 (Homo sapiens)
  • 5 RGD objects have been annotated to Scapuloperoneal myopathy  (HP:0009054)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Scapuloperoneal myopathy
  • Original References(s): PMID:23861362 PMID:25741868 PMID:28492532


  • An association has been curated linking MYH7 and Scapuloperoneal myopathy 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:10041902 (Homo sapiens)
  • 5 RGD objects have been annotated to Scapuloperoneal myopathy  (HP:0009054)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Scapuloperoneal myopathy
  • Original References(s): PMID:25741868


  • An association has been curated linking MYH7 and Scapuloperoneal myopathy 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:11615867 (Homo sapiens)
  • 5 RGD objects have been annotated to Scapuloperoneal myopathy  (HP:0009054)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Scapuloperoneal myopathy


  • An association has been curated linking MYH7 and Scapuloperoneal myopathy 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:11665390 (Homo sapiens)
  • 5 RGD objects have been annotated to Scapuloperoneal myopathy  (HP:0009054)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Scapuloperoneal myopathy


  • An association has been curated linking MYH7 and Scapuloperoneal myopathy 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:8605757 (Homo sapiens)
  • 5 RGD objects have been annotated to Scapuloperoneal myopathy  (HP:0009054)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Scapuloperoneal myopathy
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532 PMID:29300372


  • An association has been curated linking MYH7 and Scapuloperoneal myopathy 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:9833068 (Homo sapiens)
  • 5 RGD objects have been annotated to Scapuloperoneal myopathy  (HP:0009054)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Scapuloperoneal myopathy
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYH7 and Scapuloperoneal myopathy 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:11040137 (Homo sapiens)
  • 5 RGD objects have been annotated to Scapuloperoneal myopathy  (HP:0009054)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Scapuloperoneal myopathy
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:9536098


  • An association has been curated linking MYH7 and Scapuloperoneal myopathy 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:11646177 (Homo sapiens)
  • 5 RGD objects have been annotated to Scapuloperoneal myopathy  (HP:0009054)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Scapuloperoneal myopathy


  • An association has been curated linking MYH7 and Scapuloperoneal myopathy 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:11599759 (Homo sapiens)
  • 5 RGD objects have been annotated to Scapuloperoneal myopathy  (HP:0009054)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Scapuloperoneal myopathy


  • An association has been curated linking MYH7 and Scapuloperoneal myopathy 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:11665579 (Homo sapiens)
  • 5 RGD objects have been annotated to Scapuloperoneal myopathy  (HP:0009054)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Scapuloperoneal myopathy


  • An association has been curated linking MYH7 and Scapuloperoneal myopathy 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:11644402 (Homo sapiens)
  • 5 RGD objects have been annotated to Scapuloperoneal myopathy  (HP:0009054)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Scapuloperoneal myopathy


  • An association has been curated linking MYH7 and Scapuloperoneal myopathy 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:11665955 (Homo sapiens)
  • 5 RGD objects have been annotated to Scapuloperoneal myopathy  (HP:0009054)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Scapuloperoneal myopathy


  • An association has been curated linking MYH7 and Scapuloperoneal myopathy 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:11614137 (Homo sapiens)
  • 5 RGD objects have been annotated to Scapuloperoneal myopathy  (HP:0009054)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Scapuloperoneal myopathy


  • An association has been curated linking MYH7 and Scapuloperoneal myopathy 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:11613634 (Homo sapiens)
  • 5 RGD objects have been annotated to Scapuloperoneal myopathy  (HP:0009054)
  • 28 papers in RGD have been used to annotate MYH7
  • Curation Notes: ClinVar Annotator: match by term: Scapuloperoneal myopathy
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:9536098


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