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GENE - TERM ANNOTATION REPORT

9 Annotations Found.

An association has been curated linking MYO7A and Meniere's disease 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:38467832 (Homo sapiens)
  • 18 RGD objects have been annotated to Meniere's disease  (DOID:9849)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Meniere disease
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Meniere's disease 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:127286264 (Homo sapiens)
  • 18 RGD objects have been annotated to Meniere's disease  (DOID:9849)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Meniere disease
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Meniere's disease 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:11600728 (Homo sapiens)
  • 18 RGD objects have been annotated to Meniere's disease  (DOID:9849)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Meniere disease
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Meniere's disease 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:13792376 (Homo sapiens)
  • 18 RGD objects have been annotated to Meniere's disease  (DOID:9849)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Meniere disease
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30303587 PMID:30459346


  • An association has been curated linking MYO7A and Meniere's disease 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:9689647 (Homo sapiens)
  • 18 RGD objects have been annotated to Meniere's disease  (DOID:9849)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Meniere disease
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Meniere's disease 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:8606161 (Homo sapiens)
  • 18 RGD objects have been annotated to Meniere's disease  (DOID:9849)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Meniere disease
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking MYO7A and Meniere's disease 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:8605961 (Homo sapiens)
  • 18 RGD objects have been annotated to Meniere's disease  (DOID:9849)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Meniere disease
  • Original References(s): PMID:15221449 PMID:16470552 PMID:23804846 PMID:24033266 PMID:25741868 PMID:28492532 PMID:33363762


  • An association has been curated linking MYO7A and Meniere's disease 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:8606014 (Homo sapiens)
  • 18 RGD objects have been annotated to Meniere's disease  (DOID:9849)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Meniere disease
  • Original References(s): PMID:20146813 PMID:21487335 PMID:22681893 PMID:24033266 PMID:25741868 PMID:28000701 PMID:28492532


  • An association has been curated linking MYO7A and Meniere's disease 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:11603002 (Homo sapiens)
  • 18 RGD objects have been annotated to Meniere's disease  (DOID:9849)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Meniere disease
  • Original References(s): PMID:25741868 PMID:28492532


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