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GENE - TERM ANNOTATION REPORT

198 Annotations Found.

An association has been curated linking USH2A and Usher syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Auslender N, etal., Genet Test. 2008 Jun;12(2):289-94. doi: 10.1089/gte.2007.0107.
  • 4 additional annotations were made from Auslender N, etal., Genet Test. 2008 Jun;12(2):289-94. doi: 10.1089/gte.2007.0107.
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Qualifier: susceptibility
  • Curation Notes: DNA:snps, insertion:exon, intron:multiple (human)


  • An association has been curated linking USH2A 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:13782450 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:18281613 PMID:24944099 PMID:25575603 PMID:25741868 PMID:26338283 PMID:26667666 PMID:27157150 PMID:27318125 PMID:27460420 PMID:28492532 PMID:29142287 PMID:29953849 PMID:31370859 PMID:31699113 PMID:31960602 PMID:32581362 PMID:34906470 PMID:36909829


  • An association has been curated linking USH2A 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:8611216 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:17085681 PMID:17405132 PMID:19683999 PMID:19737284 PMID:21569298 PMID:21909055 PMID:24033266 PMID:25252889 PMID:2525289 PMID:25575603 PMID:25741868 PMID:27460420 PMID:28492532 PMID:28653555 PMID:28894305 PMID:30311386 PMID:34008892 PMID:36909829


  • An association has been curated linking USH2A 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:401797652 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868 PMID:36909829


  • An association has been curated linking USH2A 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:8556759 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10775529 PMID:10909849 PMID:12112664 PMID:12427073 PMID:12525556 PMID:14970843 PMID:15325563 PMID:16098008 PMID:17085681 PMID:17405132 PMID:18273898 PMID:18641288 PMID:1968399 PMID:19683999 PMID:20301515 PMID:21151602 PMID:21738395 PMID:22004887 PMID:22135276 PMID:22334370 PMID:23591405 PMID:24033266 PMID:24944099 PMID:25078356 PMID:25097241 PMID:25261458 PMID:25262649 PMID:25326637 PMID:25375654 PMID:25649381 PMID:25741868 PMID:25823529 PMID:25910913 PMID:26355662 PMID:26764160 PMID:28041643 PMID:28492532 PMID:29283788 PMID:29588463 PMID:29912909 PMID:30718709 PMID:34906470 PMID:36909829


  • An association has been curated linking USH2A 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:26910030 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:22135276 PMID:24944099 PMID:25741868 PMID:26927203 PMID:28492532 PMID:28981474 PMID:36011334


  • An association has been curated linking USH2A 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:11345567 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24944099 PMID:25333064 PMID:25741868 PMID:27208204 PMID:28492532 PMID:28559085 PMID:31877679 PMID:32531858 PMID:36909829


  • An association has been curated linking USH2A 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:14395747 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:17405132 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28492532 PMID:36909829


  • An association has been curated linking USH2A 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:401927526 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A 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:12912763 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:22952768 PMID:25649381 PMID:25741868 PMID:28492532 PMID:28559085 PMID:30718709 PMID:34906470


  • An association has been curated linking USH2A 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:9688277 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532 PMID:36909829


  • An association has been curated linking USH2A and Usher syndrome in Homo sapiens.        

  • The association was traceable author statement (TAS)
  •  
  • The annotation was made from Daiger SP, etal., Clin Genet. 2013 Aug;84(2):132-41. doi: 10.1111/cge.12203. Epub 2013 Jun 19.
  • 152 additional annotations were made from Daiger SP, etal., Clin Genet. 2013 Aug;84(2):132-41. doi: 10.1111/cge.12203. Epub 2013 Jun 19.
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A


  • An association has been curated linking USH2A 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:11638770 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25472526 PMID:25741868 PMID:28492532 PMID:34906470 PMID:35266249


  • An association has been curated linking USH2A 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:10048923 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:20507924 PMID:21151602 PMID:22004887 PMID:22135276 PMID:22334370 PMID:24033266 PMID:25097241 PMID:25472526 PMID:25649381 PMID:25741868 PMID:25999674 PMID:26667666 PMID:28041643 PMID:28492532 PMID:28559085 PMID:29953849 PMID:32531858 PMID:34906470 PMID:36909829


  • An association has been curated linking USH2A 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:21070565 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28492532 PMID:30311386 PMID:30459346 PMID:34599368 PMID:36909829


  • An association has been curated linking USH2A 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:151866963 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:14970843 PMID:19881469 PMID:25342620 PMID:25741868 PMID:28157192 PMID:28492532 PMID:30190494 PMID:36909829


  • An association has been curated linking USH2A 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:8556754 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10090909 PMID:10729113 PMID:10909849 PMID:11402400 PMID:12112664 PMID:12525556 PMID:14970843 PMID:15025721 PMID:15325563 PMID:15326663 PMID:17405132 PMID:18641288 PMID:19881469 PMID:20145675 PMID:20301515 PMID:20507924 PMID:22135276 PMID:22581970 PMID:23924366 PMID:24033266 PMID:24088041 PMID:24160897 PMID:24607488 PMID:24944099 PMID:25097241 PMID:25404053 PMID:25649381 PMID:25741868 PMID:26629787 PMID:26633545 PMID:26872967 PMID:28041643 PMID:28492532 PMID:29953849 PMID:30718709 PMID:31836858 PMID:34906470 PMID:36011334 PMID:36909829 PMID:9624053


  • An association has been curated linking USH2A 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:151781397 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29196752 PMID:36909829


  • An association has been curated linking USH2A 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:401927424 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A 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:13785874 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24944099 PMID:25741868 PMID:26927203 PMID:28492532


  • An association has been curated linking USH2A 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:13786533 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:22004887 PMID:24160897 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A 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:9692604 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:15325563 PMID:20507924 PMID:22135276 PMID:24033266 PMID:25649381 PMID:25741868 PMID:28041643 PMID:28492532 PMID:34906470


  • An association has been curated linking USH2A 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:9480355 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:20507924 PMID:25133613 PMID:25324289 PMID:25649381 PMID:25741868 PMID:26496393 PMID:26927203 PMID:27460420 PMID:28041643 PMID:28157192 PMID:28492532 PMID:29625443 PMID:29641573 PMID:30190494 PMID:30280194 PMID:30718709 PMID:31998945 PMID:32188678


  • An association has been curated linking USH2A 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:13435429 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:28041643


  • An association has been curated linking USH2A 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:8611278 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:28041643 PMID:28492532


  • An association has been curated linking USH2A 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:9690877 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:22135276 PMID:24033266 PMID:25741868 PMID:26667666 PMID:28041643 PMID:28492532 PMID:31456290 PMID:31816670 PMID:32176120 PMID:32581362 PMID:32637036 PMID:33749171


  • An association has been curated linking USH2A 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:401927520 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A 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:151734788 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A 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:9689078 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:22135276 PMID:24033266 PMID:25521520 PMID:26969326 PMID:27460420 PMID:28041643 PMID:28492532


  • An association has been curated linking USH2A 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:21405221 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:23591405 PMID:25404053 PMID:25741868 PMID:26927203 PMID:27460420 PMID:28492532 PMID:30924848 PMID:31456290 PMID:31877679 PMID:32531858 PMID:33576794 PMID:34906470


  • An association has been curated linking USH2A 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:10052925 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH2A 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:8611213 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:18273898 PMID:20507924 PMID:22135276 PMID:23591405 PMID:24033266 PMID:24265693 PMID:25741868 PMID:26969326 PMID:27318125 PMID:27460420 PMID:28041643 PMID:28492532 PMID:28559085 PMID:30718709


  • An association has been curated linking USH2A 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:8611369 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:20301442 PMID:21569298 PMID:24033266 PMID:25741868 PMID:26927203 PMID:28041643 PMID:28492532 PMID:30245029


  • An association has been curated linking USH2A 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:8611454 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:22004887 PMID:24033266 PMID:24944099 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A 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:13435441 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:28041643


  • An association has been curated linking USH2A 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:127234344 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266


  • An association has been curated linking USH2A 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:13435417 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:28041643


  • An association has been curated linking USH2A 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:11094645 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:25575603 PMID:25741868


  • An association has been curated linking USH2A 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:8611463 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:10729113 PMID:10909849 PMID:16199547 PMID:19023448 PMID:19737284 PMID:20507924 PMID:20596040 PMID:24033266 PMID:24853665 PMID:25133613 PMID:25324289 PMID:25356976 PMID:25649381 PMID:25741868 PMID:26338283 PMID:28492532


  • An association has been curated linking USH2A 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:8611470 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:19881469 PMID:20507924 PMID:24033266 PMID:25649381 PMID:25741868 PMID:28041643 PMID:28492532 PMID:28559085


  • An association has been curated linking USH2A 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:13435444 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:28041643


  • An association has been curated linking USH2A 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:13435434 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:28041643


  • An association has been curated linking USH2A 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:13435432 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:28041643


  • An association has been curated linking USH2A 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:13435414 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:16963483 PMID:17405132 PMID:18273898 PMID:21569298 PMID:24033266 PMID:24498627 PMID:25575603 PMID:25741868 PMID:27460420 PMID:28041643 PMID:28492532 PMID:28653555 PMID:29142287


  • An association has been curated linking USH2A 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:10049038 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:18273898 PMID:20440071 PMID:22135276 PMID:24033266 PMID:24944099 PMID:25521520 PMID:25741868 PMID:26416264 PMID:26927203 PMID:27460420 PMID:27957503 PMID:28041643 PMID:28492532


  • An association has been curated linking USH2A 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:13515809 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266


  • An association has been curated linking USH2A 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:13516966 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266


  • An association has been curated linking USH2A 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:13522439 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266


  • An association has been curated linking USH2A 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:13520955 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:15025721 PMID:15325563 PMID:15823922 PMID:18665195 PMID:20507924 PMID:21686329 PMID:24033266 PMID:25525159 PMID:25649381 PMID:25741868 PMID:26338283 PMID:27460420 PMID:28492532


  • An association has been curated linking USH2A 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:13522268 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:24944099


  • An association has been curated linking USH2A 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:8611381 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:17085681 PMID:17405132 PMID:20145675 PMID:20507924 PMID:22025579 PMID:24033266 PMID:25097241 PMID:26969326 PMID:28041643 PMID:28492532 PMID:28944237


  • An association has been curated linking USH2A 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:12893824 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:20591486 PMID:25741868 PMID:28041643 PMID:28492532


  • An association has been curated linking USH2A 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:9688267 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:28041643 PMID:28492532


  • An association has been curated linking USH2A 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:40889771 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:16963483 PMID:25741868 PMID:27460420 PMID:32675063


  • An association has been curated linking USH2A 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:8611319 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH2A 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:25318794 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:26352687 PMID:28492532


  • An association has been curated linking USH2A 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:11644104 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A 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:9692596 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Hallgren syndrome
  • Original References(s): PMID:23804846 PMID:24033266 PMID:25741868 PMID:27460420 PMID:28041643 PMID:28492532


  • An association has been curated linking USH2A 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:9688279 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:21738395 PMID:24033266 PMID:28041643 PMID:28492532


  • An association has been curated linking USH2A 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:150546793 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome


  • An association has been curated linking USH2A 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:11351162 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:26338283 PMID:28492532


  • An association has been curated linking USH2A 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:9689136 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:28041643 PMID:28492532


  • An association has been curated linking USH2A 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:401927360 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A 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:14698381 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:30718709


  • An association has been curated linking USH2A 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:8611440 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28041643 PMID:28492532


  • An association has been curated linking USH2A 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:11088334 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:25741868


  • An association has been curated linking USH2A 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:8611474 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:11311042 PMID:14970843 PMID:15025721 PMID:15241801 PMID:15325563 PMID:16963483 PMID:18273898 PMID:18641288 PMID:19683999 PMID:20507924 PMID:23940504 PMID:24033266 PMID:24944099 PMID:25649381 PMID:25741868 PMID:26806561 PMID:26969326 PMID:27460420 PMID:28041643 PMID:28492532 PMID:30718709 PMID:33089500 PMID:34906470 PMID:34948090


  • An association has been curated linking USH2A 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:127249386 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:16199547 PMID:20507924 PMID:22135276 PMID:25649381 PMID:28492532


  • An association has been curated linking USH2A 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:8611341 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:16963483 PMID:24033266 PMID:25741868 PMID:28041643 PMID:28492532 PMID:29767709 PMID:30245029 PMID:31429209


  • An association has been curated linking USH2A 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:8556760 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:15015129 PMID:16963483 PMID:18273898 PMID:18463160 PMID:18641288 PMID:19683999 PMID:19881469 PMID:20507924 PMID:21569298 PMID:22135276 PMID:24033266 PMID:25262649 PMID:25333064 PMID:25575603 PMID:2564938 PMID:25649381 PMID:25741868 PMID:26927203 PMID:27460420 PMID:28041643 PMID:28492532 PMID:28944237 PMID:29293505 PMID:30718709 PMID:31817543 PMID:34906470


  • An association has been curated linking USH2A 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:14743038 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking USH2A 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:11578194 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:14970843 PMID:19881469 PMID:21569298 PMID:22004887 PMID:24944099 PMID:25342620 PMID:25741868 PMID:27460420 PMID:28157192 PMID:28492532 PMID:30872814 PMID:32531858


  • An association has been curated linking USH2A 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:11051481 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:26872967 PMID:28041643 PMID:29074561


  • An association has been curated linking USH2A 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:12849599 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868 PMID:26261414 PMID:26306921 PMID:27032803 PMID:28492532 PMID:28981474 PMID:31213501 PMID:32098976


  • An association has been curated linking USH2A 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:152984330 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome


  • An association has been curated linking USH2A 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:151661201 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:34416374


  • An association has been curated linking USH2A 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:8611328 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A 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:10048792 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:18273898 PMID:23591405 PMID:25425308 PMID:25741868 PMID:27318125 PMID:28492532 PMID:28894305 PMID:28944237 PMID:34906470


  • An association has been curated linking USH2A 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:8611347 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:15241801 PMID:16098008 PMID:16963483 PMID:19683999 PMID:22004887 PMID:24033266 PMID:25262649 PMID:25999674 PMID:26467025 PMID:28041643 PMID:28492532 PMID:30245029 PMID:30718709 PMID:30872814


  • An association has been curated linking USH2A 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:9688275 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking USH2A 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:8646967 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:16199547 PMID:20507924 PMID:22025579 PMID:25649381 PMID:25741868 PMID:26667666 PMID:28492532 PMID:30796641 PMID:33089500


  • An association has been curated linking USH2A 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:8611371 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:16963483 PMID:20591486 PMID:24033266 PMID:24154662 PMID:25097241 PMID:25472526 PMID:25741868 PMID:25804404 PMID:26075083 PMID:26927203 PMID:27957503 PMID:28492532 PMID:28981474 PMID:30245029 PMID:31047384 PMID:31429209 PMID:34906470


  • An association has been curated linking USH2A 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:329846782 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome


  • An association has been curated linking USH2A 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:8556762 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:15015129 PMID:15043528 PMID:15241801 PMID:15325563 PMID:16963483 PMID:18641288 PMID:20301515 PMID:22135276 PMID:22334370 PMID:24033266 PMID:24265693 PMID:24498627 PMID:24944099 PMID:25649381 PMID:25741868 PMID:25999674 PMID:28041643 PMID:28492532 PMID:28559085


  • An association has been curated linking USH2A 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:13791944 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:15325563 PMID:15671307 PMID:16963483 PMID:17576681 PMID:20507924 PMID:25525159 PMID:25741868 PMID:28492532 PMID:32037395 PMID:9536098


  • An association has been curated linking USH2A 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:13791639 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:12112664 PMID:17576681 PMID:20497194 PMID:21151602 PMID:24516651 PMID:24944099 PMID:25366773 PMID:25741868 PMID:28492532 PMID:30190494 PMID:32188678 PMID:33576794 PMID:9536098


  • An association has been curated linking USH2A 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:8611208 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:15025721 PMID:15241801 PMID:17405132 PMID:18273898 PMID:19129697 PMID:22135276 PMID:22681893 PMID:24033266 PMID:24160897 PMID:25097241 PMID:25333064 PMID:25521520 PMID:25741868 PMID:26969326 PMID:28492532 PMID:28559085 PMID:28944237 PMID:29343940 PMID:34906470


  • An association has been curated linking USH2A 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:13795179 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868 PMID:25999674 PMID:26927203 PMID:27318125 PMID:27460420 PMID:28224992 PMID:28492532 PMID:34203967 PMID:34906470


  • An association has been curated linking USH2A 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:11643039 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:23940504 PMID:24516651 PMID:24625443 PMID:25741868 PMID:27157150 PMID:27460420 PMID:28041643 PMID:28492532 PMID:29912909 PMID:30718709 PMID:32176120 PMID:33576794 PMID:34906470


  • An association has been curated linking USH2A 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:13435412 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868 PMID:28041643


  • An association has been curated linking USH2A 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:14698513 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:21569298 PMID:25741868 PMID:26806561 PMID:27596865 PMID:28492532 PMID:28678594 PMID:29625443 PMID:30459346 PMID:30718709 PMID:31213501


  • An association has been curated linking USH2A 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:8611256 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:17576681 PMID:22135276 PMID:24033266 PMID:25649381 PMID:25741868 PMID:25910913 PMID:28492532 PMID:34906470 PMID:9536098


  • An association has been curated linking USH2A 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:13786987 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:16114888 PMID:16963483 PMID:22135276 PMID:24033266 PMID:24944099 PMID:25741868 PMID:28492532 PMID:31266775 PMID:32176120 PMID:33089500 PMID:36011334


  • An association has been curated linking USH2A 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:8643577 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:20507924 PMID:22004887 PMID:25741868 PMID:27460420 PMID:28492532 PMID:32483926 PMID:33576794 PMID:34148116 PMID:34781295 PMID:34906470


  • An association has been curated linking USH2A 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:13528922 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:17085681 PMID:19683999 PMID:20507924 PMID:22004887 PMID:24033266 PMID:25472526 PMID:25741868 PMID:28492532 PMID:29899460 PMID:30081015 PMID:32098976


  • An association has been curated linking USH2A 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:243056740 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:29266521


  • An association has been curated linking USH2A 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:13435141 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:16199547 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28041643 PMID:28492532 PMID:28559085 PMID:28981474


  • An association has been curated linking USH2A 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:126923385 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25425308 PMID:25741868 PMID:28492532 PMID:29940899 PMID:31054281 PMID:32188678 PMID:34781295


  • An association has been curated linking USH2A 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:243056709 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome


  • An association has been curated linking USH2A 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:26900482 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:22135276 PMID:24618324 PMID:25741868 PMID:26927203 PMID:28492532 PMID:29142287 PMID:29625443 PMID:31877679 PMID:34148116 PMID:34948090 PMID:36314366


  • An association has been curated linking USH2A 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:9690064 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:28157192 PMID:28492532


  • An association has been curated linking USH2A 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:9480364 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:21686329 PMID:24938718 PMID:25078356 PMID:25324289 PMID:25356976 PMID:25741868 PMID:26310143 PMID:26338283 PMID:27160483 PMID:27460420 PMID:28041643 PMID:28492532 PMID:29625443 PMID:29899460 PMID:30948794 PMID:31213501 PMID:32893482 PMID:36314366


  • An association has been curated linking USH2A 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:10403338 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:20507924 PMID:24088041 PMID:24265693 PMID:24603341 PMID:24901346 PMID:25412400 PMID:25741868 PMID:26633545 PMID:26667666 PMID:28041643 PMID:28492532 PMID:28761320 PMID:28981474 PMID:32188678


  • An association has been curated linking USH2A 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:9689727 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:17085681 PMID:24033266 PMID:25649381 PMID:26969326 PMID:28492532 PMID:31736247 PMID:32579692 PMID:32637036


  • An association has been curated linking USH2A 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:8611456 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:25133751 PMID:25741868 PMID:28041643 PMID:28492532


  • An association has been curated linking USH2A 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:151730004 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:29655801 PMID:32037395


  • An association has been curated linking USH2A 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:156451360 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome


  • An association has been curated linking USH2A 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:13785251 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:21593743 PMID:23737954 PMID:25356976 PMID:25649381 PMID:25741868 PMID:26338283 PMID:28492532 PMID:32188678 PMID:33089500 PMID:34130719


  • An association has been curated linking USH2A 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:13435428 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:27460420 PMID:28041643 PMID:28492532 PMID:28798898


  • An association has been curated linking USH2A 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:13787090 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:22135276 PMID:24033266 PMID:25333064 PMID:25558175 PMID:25649381 PMID:25741868 PMID:26766544 PMID:27460420 PMID:28492532 PMID:28559085 PMID:28944237 PMID:28981474 PMID:29196752


  • An association has been curated linking USH2A 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:8611403 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:16199547 PMID:18641288 PMID:20507924 PMID:24033266 PMID:25525159 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A 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:8568540 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:20507924 PMID:22009552 PMID:23924366 PMID:25404053 PMID:25558175 PMID:25741868 PMID:26629787 PMID:27460420 PMID:28041643 PMID:28492532 PMID:29490346 PMID:30718709


  • An association has been curated linking USH2A 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:127266624 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A 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:156451361 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome


  • An association has been curated linking USH2A 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:8689249 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:22135276 PMID:25741868 PMID:25991456 PMID:27208204 PMID:27460420 PMID:27957503 PMID:28492532 PMID:28512305 PMID:30718709


  • An association has been curated linking USH2A 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:10048775 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:17405132 PMID:17576681 PMID:20052763 PMID:22135276 PMID:24944099 PMID:25097241 PMID:25649381 PMID:25741868 PMID:26969326 PMID:27208204 PMID:27460420 PMID:28041643 PMID:28492532 PMID:9536098


  • An association has been curated linking USH2A 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:8611324 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:20507924 PMID:20591486 PMID:23591405 PMID:24033266 PMID:25741868 PMID:28041643 PMID:28492532 PMID:30718709


  • An association has been curated linking USH2A 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:9688274 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28041643 PMID:28492532 PMID:30190494 PMID:32707200


  • An association has been curated linking USH2A 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:13786000 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:24944099 PMID:25575603 PMID:25649381 PMID:25741868 PMID:28492532 PMID:32531858 PMID:34948090


  • An association has been curated linking USH2A 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:13783017 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:19737284 PMID:23737954 PMID:28492532 PMID:30029497 PMID:32188678


  • An association has been curated linking USH2A 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:13435419 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:22135276 PMID:28041643 PMID:28492532 PMID:29142287


  • An association has been curated linking USH2A 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:13783097 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:23591405 PMID:28492532 PMID:28559085 PMID:30543658 PMID:30718709 PMID:32531858


  • An association has been curated linking USH2A 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:156055899 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome


  • An association has been curated linking USH2A 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:13435055 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28041643 PMID:28492532


  • An association has been curated linking USH2A 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:13435422 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:18273898 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28041643 PMID:28492532


  • An association has been curated linking USH2A 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:11558267 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:26927203 PMID:28224992 PMID:28492532 PMID:28944237


  • An association has been curated linking USH2A 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:156054979 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29641573 PMID:31054281 PMID:32188678 PMID:32675063


  • An association has been curated linking USH2A 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:40816038 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:22135276 PMID:25741868 PMID:26355662 PMID:26667666 PMID:26856745 PMID:28492532 PMID:30902645


  • An association has been curated linking USH2A 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:9688266 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:20507924 PMID:21151602 PMID:22135276 PMID:22334370 PMID:23591405 PMID:23940504 PMID:23991284 PMID:24033266 PMID:25412400 PMID:25649381 PMID:25741868 PMID:26806561 PMID:26927203 PMID:27160483 PMID:27208204 PMID:27596865 PMID:28041643 PMID:28118666 PMID:28157192 PMID:28492532 PMID:28559085 PMID:28894305 PMID:29276052 PMID:30543658 PMID:30718709 PMID:30902645 PMID:32531858 PMID:34906470 PMID:35672425


  • An association has been curated linking USH2A 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:13517059 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25097241 PMID:25649381 PMID:25741868 PMID:28492532 PMID:31456290


  • An association has been curated linking USH2A 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:401927420 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A 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:401927485 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A 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:8611270 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:25133751 PMID:25741868 PMID:28041643 PMID:28492532


  • An association has been curated linking USH2A 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:8611451 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:15325563 PMID:18273898 PMID:20052763 PMID:22135276 PMID:24033266 PMID:24944099 PMID:25356976 PMID:25741868 PMID:26338283 PMID:27318125 PMID:27460420 PMID:28492532 PMID:28944237 PMID:29490346 PMID:29625443 PMID:30245029 PMID:32531858 PMID:32637036


  • An association has been curated linking USH2A 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:26897925 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A 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:8611357 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28041643


  • An association has been curated linking USH2A 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:13435442 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28041643 PMID:28492532 PMID:28894305


  • An association has been curated linking USH2A 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:13528408 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Hallgren syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:24033266 PMID:25649381 PMID:25741868 PMID:28492532 PMID:30337596


  • An association has been curated linking USH2A 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:26913146 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28492532 PMID:32100970


  • An association has been curated linking USH2A 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:13792018 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10738000 PMID:10909849 PMID:11311042 PMID:20507924 PMID:24367894 PMID:25649381 PMID:25741868 PMID:28492532 PMID:29490346


  • An association has been curated linking USH2A 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:8611249 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:24033266 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A 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:126773313 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:17405132 PMID:24944099 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A 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:13783566 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A 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:151828201 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A 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:21067039 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:16963483 PMID:21738395 PMID:24367894 PMID:25741868 PMID:25999674 PMID:26927203 PMID:28492532 PMID:28559085 PMID:32098976 PMID:33111345 PMID:33576794


  • An association has been curated linking USH2A 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:127243363 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:16199547 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A 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:8611309 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:18665195 PMID:20507924 PMID:22135276 PMID:24033266 PMID:25649381 PMID:25741868 PMID:26338283 PMID:28492532 PMID:30718709 PMID:31266775 PMID:31998945 PMID:32675063 PMID:33691693


  • An association has been curated linking USH2A 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:8556758 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:16963483 PMID:24033266 PMID:25741868 PMID:26969326 PMID:28492532 PMID:33089500


  • An association has been curated linking USH2A 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:13435418 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:18665195 PMID:21569298 PMID:24944099 PMID:25649381 PMID:25741868 PMID:27460420 PMID:28041643 PMID:28492532


  • An association has been curated linking USH2A 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:13434969 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:15015129 PMID:17405132 PMID:22334370 PMID:24944099 PMID:25741868 PMID:25999674 PMID:26927203 PMID:27460420 PMID:28041643 PMID:28492532 PMID:30718709 PMID:31266775 PMID:31998945 PMID:32188678 PMID:32581362


  • An association has been curated linking USH2A 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:8611471 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A 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:13789973 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:26927203 PMID:28492532 PMID:29625443


  • An association has been curated linking USH2A 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:38486113 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:26927203 PMID:27318125 PMID:28492532


  • An association has been curated linking USH2A 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:8611394 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:23737954 PMID:24033266 PMID:25356976 PMID:25741868 PMID:26310143 PMID:26338283 PMID:28492532 PMID:29625443 PMID:34416374


  • An association has been curated linking USH2A 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:13435091 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:15325563 PMID:20507924 PMID:25649381 PMID:25741868 PMID:26856745 PMID:27460420 PMID:28041643 PMID:28492532


  • An association has been curated linking USH2A 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:12905665 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A 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:156076429 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868 PMID:28492532 PMID:32675063


  • An association has been curated linking USH2A 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:8611487 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:22135276 PMID:24033266 PMID:25649381 PMID:25741868 PMID:26164827 PMID:28492532 PMID:28559085 PMID:28894305 PMID:31370859


  • An association has been curated linking USH2A 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:401927381 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A 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:401927398 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A 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:401927518 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A 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:401927443 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A 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:401927385 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A 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:13529135 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:21569298 PMID:24033266 PMID:25333064 PMID:25649381 PMID:25741868 PMID:27460420 PMID:27957503 PMID:28492532


  • An association has been curated linking USH2A 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:401927522 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A 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:401927447 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A 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:13785413 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:22135276 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A 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:8611267 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:25741868


  • An association has been curated linking USH2A 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:401927470 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A 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:38458190 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A 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:401927372 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking USH2A 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:21070571 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:16199547 PMID:20507924 PMID:24944099 PMID:25649381 PMID:25741868 PMID:26969326 PMID:28492532 PMID:34948090


  • An association has been curated linking USH2A 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:13784959 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:16199547 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28492532 PMID:30902645 PMID:31047384 PMID:31213501 PMID:33691693 PMID:33946315


  • An association has been curated linking USH2A 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:13435437 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:27624628 PMID:28041643 PMID:28492532


  • An association has been curated linking USH2A 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:151779421 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28492532 PMID:30826590 PMID:31144483 PMID:32093671 PMID:32675063 PMID:33124170 PMID:33781268


  • An association has been curated linking USH2A 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:151767010 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A 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:13435436 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868 PMID:28041643 PMID:28492532


  • An association has been curated linking USH2A 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:151861721 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A 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:9689725 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:24154662 PMID:25649381 PMID:25741868 PMID:28492532 PMID:31904091 PMID:32675063


  • An association has been curated linking USH2A 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:13788180 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:23661368 PMID:23967202 PMID:25268133 PMID:25741868 PMID:28492532 PMID:29625443 PMID:30029497 PMID:31213501 PMID:31960602 PMID:32188678


  • An association has been curated linking USH2A 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:9690648 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A 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:13782438 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:16199547 PMID:20507924 PMID:22135276 PMID:25649381 PMID:25741868 PMID:28492532 PMID:34948090


  • An association has been curated linking USH2A 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:151850598 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:25741868 PMID:27460420 PMID:28492532 PMID:31877679 PMID:35266249


  • An association has been curated linking USH2A 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:13784458 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25333064 PMID:25558175 PMID:25741868 PMID:27460420 PMID:28944237 PMID:34638692 PMID:34948090


  • An association has been curated linking USH2A 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:11559761 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:15325563 PMID:18641288 PMID:19881469 PMID:20507924 PMID:22135276 PMID:23924366 PMID:24033266 PMID:25472526 PMID:25649381 PMID:25741868 PMID:27624628 PMID:28492532 PMID:32037395 PMID:34203967


  • An association has been curated linking USH2A 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:10052387 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking USH2A 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:9690588 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:27460420


  • An association has been curated linking USH2A 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:13434961 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:15823922 PMID:18273898 PMID:19683999 PMID:20507924 PMID:22135276 PMID:24944099 PMID:25333064 PMID:25649381 PMID:25741868 PMID:26338283 PMID:27460420 PMID:28041643 PMID:28492532


  • An association has been curated linking USH2A 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:11095226 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:16199547 PMID:20507924 PMID:24033266 PMID:25649381 PMID:25741868 PMID:28492532 PMID:28944237


  • An association has been curated linking USH2A 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:401797650 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868 PMID:28492532 PMID:36909829


  • An association has been curated linking USH2A 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:11090581 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:21569298 PMID:25741868 PMID:26667666 PMID:28492532 PMID:28559085 PMID:32531858 PMID:34906470


  • An association has been curated linking USH2A 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:8629302 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868 PMID:26667666 PMID:26806561 PMID:26927203 PMID:28492532 PMID:32531858 PMID:34906470


  • An association has been curated linking USH2A 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:8611485 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:17296898 PMID:17405132 PMID:18641288 PMID:20507924 PMID:23591405 PMID:24033266 PMID:24944099 PMID:25333064 PMID:25575603 PMID:25649381 PMID:25741868 PMID:27460420 PMID:28130426 PMID:28492532 PMID:28653555 PMID:28944237 PMID:34906470


  • An association has been curated linking USH2A 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:329846783 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:20507924 PMID:25649381 PMID:28492532


  • An association has been curated linking USH2A 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:11088351 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:10729113 PMID:10909849 PMID:16199547 PMID:18273898 PMID:18641288 PMID:19683999 PMID:20507924 PMID:23591405 PMID:24033266 PMID:24944099 PMID:25097241 PMID:25525159 PMID:25558175 PMID:25575603 PMID:25649381 PMID:25741868 PMID:26355662 PMID:28492532 PMID:29074561 PMID:29490346 PMID:30311386 PMID:30459346 PMID:31456290 PMID:31589614 PMID:32037395 PMID:32176120 PMID:32552793 PMID:33576794 PMID:34426522 PMID:34906470


  • An association has been curated linking USH2A 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:13782432 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25356976 PMID:25741868 PMID:27460420 PMID:27583663 PMID:28492532 PMID:28944237 PMID:31152317 PMID:32188678 PMID:33089500 PMID:35266249


  • An association has been curated linking USH2A 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:126746349 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25324289 PMID:25741868 PMID:28492532 PMID:29641573 PMID:32100970 PMID:32188678 PMID:32319668 PMID:32893482 PMID:33090715 PMID:33124170


  • An association has been curated linking USH2A 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:401797649 (Homo sapiens)
  • 222 RGD objects have been annotated to Usher syndrome  (DOID:0050439)
  • 21 papers in RGD have been used to annotate USH2A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome
  • Original References(s): PMID:25741868 PMID:28492532 PMID:32675063 PMID:36909829


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