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GENE - TERM ANNOTATION REPORT

917 Annotations Found.

An association has been curated linking MYO7A and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Smits BM, etal., Genetics. 2005 Aug;170(4):1887-96. Epub 2005 Jun 18.
  • The annotation has been inferred from sequence orthology with Myo7a (Rattus norvegicus) [(IAGP) inferred by association of genotype and phenotype]
  • 20 additional annotations were made from Smits BM, etal., Genetics. 2005 Aug;170(4):1887-96. Epub 2005 Jun 18.
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: DNA:nonsense mutation


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Colella P, etal., PLoS One. 2013 Aug 26;8(8):e72027. doi: 10.1371/journal.pone.0072027. eCollection 2013.
  • The annotation has been inferred from sequence orthology with Myo7a (Mus musculus) [(IMP) inferred from mutant phenotype]
  • 5 additional annotations were made from Colella P, etal., PLoS One. 2013 Aug 26;8(8):e72027. doi: 10.1371/journal.pone.0072027. eCollection 2013.
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred from direct assay (IDA)
  •  
  • The annotation was made from Colella P, etal., PLoS One. 2013 Aug 26;8(8):e72027. doi: 10.1371/journal.pone.0072027. eCollection 2013.
  • 5 additional annotations were made from Colella P, etal., PLoS One. 2013 Aug 26;8(8):e72027. doi: 10.1371/journal.pone.0072027. eCollection 2013.
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Qualifier: treatment


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8654905 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:21569298 PMID:22898263 PMID:25404053 PMID:25741868 PMID:28492532 PMID:30303587 PMID:36909829 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Najera C, etal., Hum Mutat. 2002 Jul;20(1):76-7.
  • 5 additional annotations were made from Najera C, etal., Hum Mutat. 2002 Jul;20(1):76-7.
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: DNA:mutations: :multiple


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Weston MD, etal., Am J Hum Genet. 1996 Nov;59(5):1074-83.
  • 2 additional annotations were made from Weston MD, etal., Am J Hum Genet. 1996 Nov;59(5):1074-83.
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: DNA:mutations: :multiple


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606114 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16679490 PMID:18484607 PMID:21738395 PMID:24033266 PMID:25558175 PMID:26467025 PMID:27460420 PMID:28472130 PMID:28492532 PMID:29142287 PMID:34148116 PMID:34948090


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40904330 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13791871 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:19299023 PMID:23451214 PMID:27344577 PMID:28492532 PMID:33724713 PMID:35640668


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13790080 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:23967202 PMID:25741868 PMID:34426522 PMID:35453549


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150431547 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9690585 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16470552 PMID:17576681 PMID:20052763 PMID:24033266 PMID:25404053 PMID:27460420 PMID:27957503 PMID:28492532 PMID:28944237 PMID:30459346 PMID:32531858 PMID:9536098


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11599617 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532 PMID:30311386


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11094352 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532 PMID:30311386 PMID:30718709


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9689808 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606081 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532 PMID:30311386


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606046 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:17576681 PMID:24033266 PMID:25741868 PMID:28492532 PMID:9536098


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606095 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16400615 PMID:22135276 PMID:24033266 PMID:25404053 PMID:28492532 PMID:29490346 PMID:31266775 PMID:32747562 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14742572 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11615698 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:127299199 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28911267 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13522487 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906076 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38458821 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906418 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13518940 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605963 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906077 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38496591 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8562777 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:16470552 PMID:20613545 PMID:20844544 PMID:24033266 PMID:25404053 PMID:28451532 PMID:28492532 PMID:30358468 PMID:31054281 PMID:7568224 PMID:7870171 PMID:8900236 PMID:9002678


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606112 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:10930322 PMID:16679490 PMID:18323324 PMID:18463160 PMID:18484607 PMID:21311020 PMID:21436283 PMID:21873662 PMID:22135276 PMID:24033266 PMID:25741868 PMID:26226137 PMID:28492532 PMID:28944237


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:12738598 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16963483 PMID:24033266 PMID:25404053 PMID:25525159 PMID:26969326 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8562781 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:15043528 PMID:18700726 PMID:24199935 PMID:27957503 PMID:28492532 PMID:7568224 PMID:7870171


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606168 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:16400615 PMID:18463160 PMID:21873662 PMID:24033266 PMID:25404053 PMID:26969326 PMID:27344577 PMID:28492532 PMID:30390570 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11639745 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906416 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906085 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906087 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606123 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:21873662 PMID:22135276 PMID:24033266 PMID:25404053 PMID:25741868 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906073 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606106 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:10094549 PMID:10930322 PMID:15043528 PMID:16679490 PMID:18463160 PMID:21873662 PMID:24033266 PMID:25404053 PMID:28492532 PMID:28559085 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606152 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:16199547 PMID:23591405 PMID:24033266 PMID:24164807 PMID:25404053 PMID:25741868 PMID:27743452 PMID:28492532 PMID:28944237 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906086 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606049 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:17361009 PMID:21436283 PMID:24033266 PMID:25404053 PMID:25741868 PMID:26969326 PMID:27460420 PMID:28041643 PMID:28492532 PMID:30337596 PMID:31479088 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40905424 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606130 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:26467025 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606117 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:15660226 PMID:16963483 PMID:20844544 PMID:21569298 PMID:21873662 PMID:22135276 PMID:24033266 PMID:25741868 PMID:27460420 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8562791 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:15660226


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11094040 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11096057 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:21436283 PMID:24033266 PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40905422 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13211593 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:22135276 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38458815 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9690539 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8562779 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:7568224


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8562786 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:11391666 PMID:7951250 PMID:9171833


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:10051443 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605960 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:17361009 PMID:23451239 PMID:24033266 PMID:25741868 PMID:27460420 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606022 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11636637 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606086 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605969 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:10930322 PMID:15660226 PMID:16470552 PMID:24033266 PMID:25741868 PMID:28492532 PMID:8900236 PMID:9382091


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606083 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:10094549 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40905420 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606005 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16199547 PMID:16679490 PMID:20497194 PMID:21436283 PMID:21569298 PMID:24033266 PMID:25404053 PMID:25741868 PMID:25798947 PMID:28492532 PMID:31479088 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606119 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606073 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606099 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:10094549 PMID:10425080 PMID:12112664 PMID:16679490 PMID:16963483 PMID:17960123 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606126 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9691036 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906423 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606035 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:10425080 PMID:10447383 PMID:12112664 PMID:15043528 PMID:16470552 PMID:16652077 PMID:16679490 PMID:18181211 PMID:21311020 PMID:21436283 PMID:23451239 PMID:25741868 PMID:26791358 PMID:27460420 PMID:28492532 PMID:30303587


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606077 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606094 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906420 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606166 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606116 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:10094549 PMID:10930322 PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606127 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606140 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:26467025 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606082 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606058 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532 PMID:9382091


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606067 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606146 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:10094549 PMID:16470552 PMID:24033266 PMID:26467025 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606151 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28868610 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606118 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:10930322 PMID:24033266 PMID:24194196 PMID:25468891 PMID:25741868 PMID:28492532 PMID:30303587


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26910584 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:10094549 PMID:10930322 PMID:18463160 PMID:25333064 PMID:25741868 PMID:26969326 PMID:28000701 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606055 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:10930322 PMID:24033266 PMID:25468891 PMID:26969326 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38491027 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15123043 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15116684 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:151763296 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15165943 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15173500 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15175957 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26915068 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906428 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15175168 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15184656 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15171243 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15151732 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40905418 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15123215 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15123046 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15131740 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15183128 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15141960 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15142081 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26890621 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906417 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15137189 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15172245 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906088 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9690736 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15139412 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13526728 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15145997 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15163453 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:21074076 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26921384 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15101634 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26911525 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906071 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26898894 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26912815 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15150103 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15187152 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26914520 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606147 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26884737 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:12907078 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9690320 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:21569298 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15108996 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15138282 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15162790 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26920208 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906425 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14396763 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15126522 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26887618 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15111424 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13704203 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906419 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40905416 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11095948 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906427 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38499962 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15123272 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15194003 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40904324 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606092 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:20146813 PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26914833 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606125 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606132 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606148 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:24831256 PMID:25472526 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605977 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:16470552 PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40905419 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15161537 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15124729 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40905423 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906421 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606090 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:20146813 PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606048 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:26467025 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14711860 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606004 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:26969326 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606015 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13539328 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:22135276 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9692042 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606109 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15123426 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606069 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606096 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906074 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11614146 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15187361 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15114411 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15117538 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9689640 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14736369 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906426 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40905417 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906083 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605980 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40904335 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15125027 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15146998 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26885082 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40904333 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11643947 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26884591 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38495440 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26886995 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906072 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40904321 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606102 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:10930322 PMID:15043528 PMID:16963483 PMID:18463160 PMID:20613545 PMID:21873662 PMID:22785243 PMID:24033266 PMID:28492532 PMID:9718356


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26914345 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26911445 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605968 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40904323 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14703388 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26897533 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606011 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606019 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11351106 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606007 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11616457 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606032 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:15121790 PMID:15221449 PMID:15300860 PMID:21150918 PMID:24033266 PMID:28492532 PMID:9354784


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606051 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606056 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:17361009 PMID:20146813 PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606158 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:10930322 PMID:24033266 PMID:28439001


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15106012 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606142 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606047 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11618161 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14705027 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:15606003 PMID:19299023 PMID:24033266 PMID:28008688 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:10051935 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26915810 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40904326 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26920968 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9689637 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906424 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9690116 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40904331 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906430 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11617524 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906084 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689647 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9689626 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9689631 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906432 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13541132 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:10050400 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40904332 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:12743190 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11648103 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11651536 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13783578 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:23804846


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:21405074 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:32747562


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13792235 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:17361009 PMID:27460420


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14724900 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13789861 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16199547 PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13782578 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16400615 PMID:16679490 PMID:21436283 PMID:25404053 PMID:28492532 PMID:33576163 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28867480 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28867483 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11601330 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13782753 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:127246792 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11599142 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11652556 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606062 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:26338283 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13785642 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28870650 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13792160 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11546842 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11550050 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13787734 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:27460420


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28867374 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13535377 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11645360 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14715857 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11603522 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13790943 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25558175


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11602958 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28867787 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14715779 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:127328645 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11543819 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:12743283 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9689644 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:26467025 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11601443 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9689634 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14726055 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13792016 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13791900 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605988 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11650480 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8653206 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11618003 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606006 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type I, French variety
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150413367 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14715781 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9690931 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150413556 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13788899 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:16199547 PMID:25404053 PMID:28492532 PMID:29416772 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28868460 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11095683 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14724903 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28873422 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13788162 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606052 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13784740 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:22334370 PMID:28000701 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606167 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9689641 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11543464 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11604839 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606149 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13783717 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28870258 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11092349 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13783782 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28868962 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8606161 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11092239 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11646256 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13791618 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28871870 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606107 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13787306 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11094023 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13790718 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28871530 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:10930322 PMID:24033266 PMID:26467025 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28911205 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150338164 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28911024 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9689636 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13788492 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:22135276


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13787204 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:26633542


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:151348331 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28492532 PMID:32747562


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13782574 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150338166 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11615560 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9690945 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606050 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11598827 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13788004 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606103 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606111 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:17361009 PMID:19683999 PMID:20146813 PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13791854 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25373420 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13785602 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150451208 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11617290 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150461076 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28911372 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28911745 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11351236 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:27208204


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9687988 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11645653 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13785408 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16679490 PMID:17361009 PMID:27460420


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28873622 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14736389 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606779 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11599332 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9689643 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13787475 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24831256


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11604683 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606017 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13784483 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28868326 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13783804 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13790585 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150338168 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13783400 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25373420 PMID:27911912


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150413365 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11549888 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13784602 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28873186 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13789363 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13786660 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11648023 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606076 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11647817 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14703788 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606138 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13789588 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13785285 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9689630 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13787952 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9689635 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:20052763 PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13784869 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11647376 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13528200 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606075 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9690967 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:22135276 PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13789383 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:19299023 PMID:28492532 PMID:32428919


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28911478 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13789172 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:26011067


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13790312 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:19074810 PMID:9171832


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606157 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40904336 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150338153 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28911027 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14736349 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14715867 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9687992 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11613766 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13788493 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16199547 PMID:18181211 PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606110 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:26467025 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126749970 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28911477 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28868189 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28911431 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13783349 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28911648 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11600078 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13784460 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14715795 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28871170 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24105371 PMID:26309859 PMID:26338283 PMID:27460420 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14726057 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9688495 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13783111 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16963483 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11652481 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14715772 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606059 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11650750 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13519519 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13515241 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11604483 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13787972 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:27068579


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11600519 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13791626 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24498627


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11549018 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13533332 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13789822 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13787521 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28911111 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9689628 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:21569298 PMID:24033266 PMID:25262649 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11598762 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606013 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:15300860 PMID:23804846 PMID:24033266 PMID:25741868 PMID:28492532 PMID:32097363


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28872464 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150413371 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:10048787 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16963483 PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606008 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9689627 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606024 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606041 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13534633 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13787918 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:10094549 PMID:16963483


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28911025 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28872088 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605993 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13787092 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12112664 PMID:16470552 PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14715792 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14715859 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13786474 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24164807


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13789217 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24105371 PMID:25741868 PMID:26309859 PMID:26338283 PMID:27460420 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13789202 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11617187 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606155 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type I, French variety
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28910270 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606145 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type I, French variety
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28911430 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150338169 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150338171 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11648301 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28911026 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11617240 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13788119 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11643712 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605976 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14715785 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14715799 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14715854 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11614042 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11615214 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13786513 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605983 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15123725 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13787537 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:27068579


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606042 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:23237960 PMID:24033266 PMID:24831256 PMID:25788563 PMID:27610647 PMID:28492532 PMID:30311386


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11648201 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606120 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13782826 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:10094549 PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13789226 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11648532 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606139 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11547072 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11544877 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150413499 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9687989 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9689769 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606053 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606000 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13789795 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11649142 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11604574 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13785357 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13525590 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9692041 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9690218 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13791079 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24618850 PMID:25404053 PMID:27460420 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28868334 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28910517 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11093182 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606071 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13785151 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16199547 PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28868462 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13784488 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:23770805 PMID:25741868 PMID:27573290 PMID:28492532 PMID:30303587


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13786102 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16470552 PMID:17576681 PMID:20497194 PMID:23451239 PMID:24997346 PMID:28492532 PMID:9536098


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11090492 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38456563 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13530168 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:10930322 PMID:25404053 PMID:25741868 PMID:27743452 PMID:28492532 PMID:30459346 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13796436 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25404053 PMID:25741868 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13523182 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:17361009 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13525090 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26887548 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605996 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:21436283 PMID:21569298 PMID:24033266 PMID:25333064 PMID:25404053 PMID:25741868 PMID:25788563 PMID:27460420 PMID:28041643 PMID:28492532 PMID:8900236 PMID:9718356


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606045 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:10094549 PMID:10930322 PMID:15043528 PMID:16400615 PMID:16652077 PMID:16679490 PMID:17361009 PMID:18463160 PMID:18484607 PMID:19683999 PMID:20513143 PMID:21569298 PMID:21873662 PMID:22135276 PMID:24033266 PMID:24199935 PMID:25525159 PMID:25741868 PMID:28041643 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13782431 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:20052763 PMID:21311020 PMID:21436283 PMID:25741868 PMID:28492532 PMID:30303587 PMID:33187236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606033 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:21436283 PMID:23208854 PMID:24033266 PMID:25741868 PMID:26486028 PMID:26969326 PMID:27068579 PMID:27160483 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:21072051 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532 PMID:30303587


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38490718 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38458756 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13788197 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:23967202 PMID:25741868 PMID:26346818 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606054 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:20052763 PMID:21436283 PMID:23770805 PMID:24033266 PMID:25741868 PMID:28492532 PMID:33576163


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14703785 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38494610 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606003 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11095847 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13435435 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:27344577 PMID:28041643 PMID:30303587 PMID:33187236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13784963 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:21569298 PMID:25404053 PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13783105 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16199547 PMID:25404053 PMID:25741868 PMID:28492532 PMID:29490346 PMID:31456290 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906081 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906075 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9691156 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:21602428 PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38475490 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:151863451 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28492532 PMID:34837038


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26921521 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13797537 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30303587 PMID:36147510


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13792226 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:16679490 PMID:21436283 PMID:21873662 PMID:26561413 PMID:26969326 PMID:27583663 PMID:28492532 PMID:31479088 PMID:35551639


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13435440 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:26654877 PMID:27460420 PMID:28041643 PMID:28492532 PMID:31479088


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605966 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:20146813 PMID:24033266 PMID:26164827 PMID:28492532 PMID:33297549


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13786594 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:27344577 PMID:27460420 PMID:28492532 PMID:31479088 PMID:33297549


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9692040 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532 PMID:29490346 PMID:32747562


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126761938 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13527222 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:35802133 PMID:36633841


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11612450 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38485332 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606162 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:24498627 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8562778 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:21436283 PMID:22219650 PMID:24033266 PMID:25404053 PMID:25741868 PMID:27460420 PMID:27610647 PMID:28492532 PMID:29490346 PMID:32747562 PMID:7568224 PMID:7870171 PMID:8900236 PMID:9002678


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605989 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25133751 PMID:25741868 PMID:27911912 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8562780 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:15043528 PMID:19299023 PMID:21873662 PMID:22135276 PMID:24033266 PMID:24199935 PMID:25741868 PMID:25788563 PMID:27460420 PMID:27583663 PMID:28492532 PMID:7568224 PMID:7870171 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606020 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11616815 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:12741315 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532 PMID:33105617


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13784944 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:23770805 PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13782608 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:26338283 PMID:27460420 PMID:27610647 PMID:28492532 PMID:29625443 PMID:35802133 PMID:36633841


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13783188 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:18700726 PMID:20497194 PMID:20613545 PMID:23591405 PMID:25741868 PMID:28492532 PMID:28944237 PMID:9382091


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26896218 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9692039 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9690874 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:17576681 PMID:24033266 PMID:28492532 PMID:9536098


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906431 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11092098 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:12835262 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:16963483 PMID:20613545 PMID:21738395 PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8568007 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:15121790 PMID:15221449 PMID:15300860 PMID:21150918 PMID:23383098 PMID:24033266 PMID:25741868 PMID:25788563 PMID:27911912 PMID:28492532 PMID:9354784


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13787809 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28281779


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:12743044 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8606014 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:20146813 PMID:21487335 PMID:22681893 PMID:24033266 PMID:25741868 PMID:28000701 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38473115 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26893138 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13435445 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:10930322 PMID:23770805 PMID:26309859 PMID:26338283 PMID:28041643 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:127312780 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38460114 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14396762 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606034 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126923554 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606093 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38490123 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13528855 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38486664 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13538145 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13533501 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:19299023 PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13536191 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11642810 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14705030 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13790524 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:19074810 PMID:24618850 PMID:25741868 PMID:27460420 PMID:27610647 PMID:27729122 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13790465 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24105371 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8605961 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:15221449 PMID:16470552 PMID:23804846 PMID:24033266 PMID:25741868 PMID:28492532 PMID:33363762


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9687987 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:18181211 PMID:22135276 PMID:24033266 PMID:25558175 PMID:28492532 PMID:30303587 PMID:33269433


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26917308 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:22135276 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126917314 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26914681 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28868960 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126756500 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150440873 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38470616 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126729299 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38497964 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11614831 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:127303767 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606080 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126749118 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605962 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:16963483 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9689645 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15111789 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15117248 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11637224 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38461762 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26898453 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606009 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606100 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126738249 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150407927 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126916022 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126761942 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38480234 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11601594 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:27610647 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11600728 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38498563 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15121036 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13516406 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:21901789 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38475638 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126758034 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26901238 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:10045081 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:27766948 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11615900 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126752455 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126908512 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606144 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26910205 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:19074810 PMID:25404053 PMID:25741868 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606087 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38498133 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15172252 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126768977 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126737857 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26919406 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26903551 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126918512 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38486562 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11602953 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:12906743 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13515913 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28872958 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26892424 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14705033 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:26011067


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11638189 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38487678 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38467832 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26889161 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38489914 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13504512 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26918105 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15179155 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13471791 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15153691 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13785997 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:26969326 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126771406 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126769150 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126759307 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38498067 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126917081 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150452622 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11618324 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:23226338 PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38499484 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38456622 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606128 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:15121790 PMID:20146813 PMID:22135276 PMID:23804846 PMID:24033266 PMID:25558175 PMID:27068579 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11091228 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26898814 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13529538 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:26467025 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126741655 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38474202 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606160 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13788565 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:26969326 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150433129 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9690495 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606113 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:19683999 PMID:20146813 PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606079 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:12112664 PMID:16679490 PMID:16963483 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13539509 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126747899 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38470800 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28911791 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126769336 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150415663 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11643501 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532 PMID:9171832


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:127281495 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38474804 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38491501 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26899728 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26916504 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606097 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:16679490 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26889481 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126772434 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126745201 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26890012 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26891185 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126756513 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:21072053 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126917772 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606010 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126923030 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606028 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13792376 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30303587 PMID:30459346


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605985 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126731563 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126908586 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126922303 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606068 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11600206 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126919754 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:127325722 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605972 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38458031 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150426784 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11602083 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606088 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126759811 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13789678 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:16470552 PMID:21436283 PMID:25404053 PMID:25741868 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150427556 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606089 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:15660226 PMID:16400615 PMID:16679490 PMID:21436283 PMID:21569298 PMID:24033266 PMID:24831256 PMID:25404053 PMID:25741868 PMID:26969326 PMID:27460420 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126917083 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606012 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38497844 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:18463160 PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126758760 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38470819 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126762088 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606026 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606027 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9689638 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14708685 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606154 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:10094549 PMID:16470552 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532 PMID:9382091


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38494676 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13535833 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38459003 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38495688 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38500015 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126740570 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15126000 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26902319 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26890917 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126735777 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38490796 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13787758 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:27460420 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126733501 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13541505 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13516657 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9687985 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:16679490 PMID:20052763 PMID:21436283 PMID:24033266 PMID:26969326 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126731095 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11641365 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:12906345 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14743162 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26886834 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15110989 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605965 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16199547 PMID:24033266 PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605970 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:15823922 PMID:16199547 PMID:24033266 PMID:25404053 PMID:25741868 PMID:26445815 PMID:27460420 PMID:28492532 PMID:30311386 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606023 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:10930322 PMID:15660226 PMID:17576681 PMID:19074810 PMID:22135276 PMID:24033266 PMID:24199935 PMID:25468891 PMID:25472526 PMID:25741868 PMID:26969326 PMID:27460420 PMID:28492532 PMID:9536098


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606061 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:22135276 PMID:24033266 PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9689639 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13537567 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14703783 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606044 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25404053 PMID:28492532 PMID:28731162 PMID:30029497 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40904322 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11088212 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9689462 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605990 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16199547 PMID:24033266 PMID:25404053 PMID:25468891 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:151855434 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:22135276 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126760562 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11093626 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25342930 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13792389 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16470552 PMID:18700726 PMID:20497194 PMID:23148716 PMID:23591405 PMID:25741868 PMID:28492532 PMID:28944237 PMID:30459346 PMID:9382091


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:12738501 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:23591405 PMID:25404053 PMID:25741868 PMID:28492532 PMID:30358468 PMID:31456290 PMID:32860223 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38469726 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:9536098


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40905414 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:9536098


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126910786 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:30311386


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11600862 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150451195 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8562782 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:16963483 PMID:18700726 PMID:21569298 PMID:21738395 PMID:22135276 PMID:24033266 PMID:25741868 PMID:28492532 PMID:3130723 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:15101155 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8562790 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:10094549 PMID:15043528 PMID:15660226 PMID:21569298 PMID:24033266 PMID:25404053 PMID:25741868 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13786840 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:23451239 PMID:25404053 PMID:25741868 PMID:27460420 PMID:28492532 PMID:8900236 PMID:9382091


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14725104 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16963483 PMID:25404053 PMID:25741868 PMID:27957503 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606141 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:19074810 PMID:21569298 PMID:22135276 PMID:24033266 PMID:25404053 PMID:25741868 PMID:28492532 PMID:30459346 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:151661250 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13540424 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:151661210 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11652698 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606002 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:15028842 PMID:16199547 PMID:19074810 PMID:24033266 PMID:25404053 PMID:25741868 PMID:26467025 PMID:28492532 PMID:33111345 PMID:8900236 PMID:9382091


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40904327 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:127234662 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605997 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:16679490 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13791069 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:27068579 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606085 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532 PMID:9718356


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606016 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9688950 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:18181211 PMID:22135276 PMID:23770805 PMID:24033266 PMID:24875298 PMID:25741868 PMID:27460420 PMID:28492532 PMID:29490346 PMID:30245029 PMID:30881389 PMID:9382091


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13532677 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606105 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605987 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:27068579 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38485327 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26905161 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606115 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16679490 PMID:16963483 PMID:23208854 PMID:25741868 PMID:27068579 PMID:28000701 PMID:28472130 PMID:28492532 PMID:29196752


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126915848 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9690059 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38493361 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9688951 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:19074810 PMID:21873662 PMID:24033266 PMID:25211151 PMID:25741868 PMID:28492532 PMID:29048421 PMID:9002678


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13540429 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11603002 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13791595 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25404053 PMID:26338283 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:21070353 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532 PMID:29178603


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13791151 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:23237960 PMID:23967202 PMID:28492532 PMID:33924653


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26905005 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25404053 PMID:26338283 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13789158 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:26338283 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11088638 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28867477 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:127262718 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:16199547 PMID:25404053 PMID:28492532 PMID:30029497 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38489058 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:16199547 PMID:25404053 PMID:28041643 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13525620 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:24831256 PMID:28492532 PMID:29625443


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38458814 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8562788 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25404053 PMID:28492532 PMID:8900236 PMID:9843659


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13791241 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:15823922 PMID:16679490 PMID:26969326 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606121 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13785305 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16199547 PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13435420 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:18181211 PMID:22135276 PMID:25404053 PMID:28041643 PMID:28492532 PMID:30303587 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605991 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:19074810 PMID:24033266 PMID:25404053 PMID:25741868 PMID:28492532 PMID:8900236 PMID:9718356


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11094770 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532 PMID:30733538


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13789692 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16199547 PMID:25404053 PMID:27068579 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13525853 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13705477 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40904325 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606063 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13787352 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16199547 PMID:16963483 PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150410583 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606122 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:21117948 PMID:24033266 PMID:25741868 PMID:27460420 PMID:28492532 PMID:32853555


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11612950 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13786113 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16679490 PMID:21436283 PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13786973 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:10094549 PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13790684 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16199547 PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9687993 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606136 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:10930322 PMID:12112664 PMID:15823922 PMID:16400615 PMID:16679490 PMID:17361009 PMID:19683999 PMID:21436283 PMID:22135276 PMID:24033266 PMID:25404053 PMID:25741868 PMID:26872967 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150451218 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:12858903 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25404053 PMID:28492532 PMID:29490346 PMID:32747562 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606150 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:16470552 PMID:18181211 PMID:19683999 PMID:20497194 PMID:21436283 PMID:22135276 PMID:23451239 PMID:24033266 PMID:24199935 PMID:25468891 PMID:25741868 PMID:26969326 PMID:28492532 PMID:9382091


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13785126 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:10868224 PMID:16199547 PMID:22135276 PMID:24199935 PMID:25404053 PMID:27460420 PMID:28492532 PMID:31479088 PMID:8900236 PMID:9171832


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:12893352 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16199547 PMID:25404053 PMID:28492532 PMID:29490346 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606072 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28910986 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13788552 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13783412 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:18700726 PMID:25741868 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:10051350 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:26969326 PMID:27344577 PMID:27460420 PMID:28492532 PMID:31479088


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13788886 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16199547 PMID:25404053 PMID:27729122 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38458577 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8562789 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:10094549 PMID:19074810 PMID:24033266 PMID:25404053 PMID:27957503 PMID:28492532 PMID:30303587 PMID:30718709 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:12859013 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:23882135 PMID:25404053 PMID:28492532 PMID:29490346 PMID:32747562 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26891253 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:18181211 PMID:25404053 PMID:25741868 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906415 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40905421 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11599798 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:17576681 PMID:24033266 PMID:28492532 PMID:9536098


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11651366 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906422 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150424734 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:20844544 PMID:21569298 PMID:21873662 PMID:22135276 PMID:27460420 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13785306 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13789970 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16199547 PMID:23559863 PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11613701 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606040 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906082 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13792478 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:27068579 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150417621 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11599056 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906079 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11090594 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606159 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13790055 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:15660226 PMID:19156839 PMID:24853665 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11096032 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:22903915 PMID:24033266 PMID:26445815 PMID:28492532 PMID:30733538 PMID:32467589 PMID:32747562


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150413563 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9690620 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13525624 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:16963483 PMID:22690115 PMID:23237960 PMID:24033266 PMID:25404053 PMID:25525159 PMID:25741868 PMID:27460420 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13790672 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16199547 PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9690788 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28868612 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38456571 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532 PMID:30459346


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38474584 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25080338 PMID:25211151 PMID:25404053 PMID:25741868 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606018 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11644321 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28869853 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13789033 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16963483 PMID:20613545 PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40904329 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13792256 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:18181211 PMID:25404053 PMID:28492532 PMID:30303587 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906080 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13522366 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:17576681 PMID:18181211 PMID:20052763 PMID:22135276 PMID:25404053 PMID:28492532 PMID:9536098


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906078 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38491616 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532 PMID:32747562 PMID:33089500


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9689646 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:23770805 PMID:24033266 PMID:25404053 PMID:25468891 PMID:27208204 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:12742546 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16679490 PMID:20052763 PMID:21436283 PMID:27957503 PMID:28492532 PMID:33576794 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13540806 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16470552 PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13789180 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532 PMID:28968992 PMID:30358468


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13785437 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24498627 PMID:25741868 PMID:28492532 PMID:33576163 PMID:33576794


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150488248 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:38499760 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13788636 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16199547 PMID:25404053 PMID:27460420 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:12742174 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:19683999 PMID:25404053 PMID:25741868 PMID:28492532 PMID:33576163 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40904328 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13788166 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16199547 PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40906429 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13783524 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:15660226 PMID:16199547 PMID:22135276 PMID:23770805 PMID:24199935 PMID:25404053 PMID:28492532 PMID:28559085 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13785434 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25404053 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26902188 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:22135276 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606030 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:17576681 PMID:24033266 PMID:25741868 PMID:28492532 PMID:9536098


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:127240237 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25404053 PMID:27583663 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9688930 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:16199547 PMID:24033266 PMID:25404053 PMID:25741868 PMID:27440999 PMID:27583663 PMID:28492532 PMID:8900236 PMID:9382091


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred from experiment (EXP)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9690849 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25404053 PMID:25741868 PMID:28492532 PMID:28944237 PMID:29048421 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13525487 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16963483 PMID:22135276 PMID:23770805 PMID:24033266 PMID:25404053 PMID:25741868 PMID:27460420 PMID:28492532 PMID:29692870 PMID:30303587 PMID:31479088 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9688940 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:15660226 PMID:16963483 PMID:18700726 PMID:22135276 PMID:24033266 PMID:25080338 PMID:25575603 PMID:27460420 PMID:28492532 PMID:34148116 PMID:9002678 PMID:9259201


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:126745185 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:10425080 PMID:15043528 PMID:21436283 PMID:25741868 PMID:28492532 PMID:35802133 PMID:36633841


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:26900412 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:10052268 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9689629 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13792356 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11090925 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532 PMID:29276601 PMID:30311386


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9688941 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:12112664 PMID:16470552 PMID:20513143 PMID:21436283 PMID:24033266 PMID:25558175 PMID:28492532 PMID:30245029 PMID:33576163 PMID:34948090


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606021 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:22135276 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532 PMID:30311386 PMID:30828346


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28870993 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:150491874 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:40905415 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28867469 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28911693 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:9690673 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532 PMID:30303587 PMID:30459346 PMID:31964843


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:401798199 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25404053 PMID:28492532 PMID:33724713 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13788800 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11095726 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:16963483 PMID:24033266 PMID:28492532 PMID:34416374


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8606066 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:16470552 PMID:21311020 PMID:24033266 PMID:25741868 PMID:28492532 PMID:30245029 PMID:31964843 PMID:33576163 PMID:36672771


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13526692 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:22135276 PMID:24033266 PMID:28492532 PMID:30303587


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:28869618 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13788725 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25404053 PMID:28492532 PMID:29625443 PMID:31035849 PMID:31541171 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:21072061 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:26226137 PMID:27460420 PMID:28492532 PMID:33089500


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:14703780 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:11090304 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:10930322 PMID:15660226 PMID:17576681 PMID:19074810 PMID:22135276 PMID:24033266 PMID:24199935 PMID:25468891 PMID:25472526 PMID:26969326 PMID:28492532 PMID:36164746 PMID:9536098


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:13792360 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25404053 PMID:25741868 PMID:26969326 PMID:28492532 PMID:8900236


  • An association has been curated linking MYO7A and Usher Syndrome Type 1B 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:8605978 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 19 papers in RGD have been used to annotate MYO7A
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:10930322 PMID:16679490 PMID:21569298 PMID:21873662 PMID:24033266 PMID:25425308 PMID:25468891 PMID:25741868 PMID:28492532 PMID:32165824 PMID:34948090


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