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GENE - TERM ANNOTATION REPORT

7 Annotations Found.

An association has been curated linking WHRN and Usher syndrome 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:8608525 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate WHRN
  • Curation Notes: ClinVar Annotator: match by term: Hallgren syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking WHRN and Usher syndrome 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:8608538 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate WHRN
  • Curation Notes: ClinVar Annotator: match by term: Hallgren syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking WHRN and Usher syndrome 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:8608511 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate WHRN
  • Curation Notes: ClinVar Annotator: match by term: Hallgren syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking WHRN and Usher syndrome 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:8608541 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate WHRN
  • Curation Notes: ClinVar Annotator: match by term: Hallgren syndrome
  • Original References(s): PMID:21569298 PMID:24033266 PMID:28492532


  • An association has been curated linking WHRN and Usher syndrome 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:8556949 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate WHRN
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:11973626 PMID:12833159 PMID:15841483 PMID:22147658 PMID:28492532


  • An association has been curated linking WHRN and Usher syndrome 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:150545480 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate WHRN
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome


  • An association has been curated linking WHRN and Usher syndrome 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:401927462 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 6 papers in RGD have been used to annotate WHRN
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868


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