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GENE - TERM ANNOTATION REPORT

284 Annotations Found.

An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608849 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:24033266 PMID:24416283 PMID:25356970 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28879555 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8689243 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1B
  • Original References(s): PMID:25991456 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11095109 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608745 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608934 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:18429043 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689971 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608942 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126751183 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:17850630 PMID:22899989 PMID:25741868 PMID:25963016 PMID:27627659 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13531985 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608770 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26969326 PMID:28492532 PMID:30311386


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691485 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11665230 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11096083 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11600466 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608774 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608943 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:18429043 PMID:24033266 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11665729 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10050457 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11579305 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608883 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11577524 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type I, French variety
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11598858 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608880 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608936 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608941 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:24416283 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608944 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608835 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608753 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:18429043 PMID:21228398 PMID:21569298 PMID:22135276 PMID:22995991 PMID:24033266 PMID:25474345 PMID:25741868 PMID:28492532 PMID:30029624 PMID:30718709


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11091706 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689825 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28905031 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15127969 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608779 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608817 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608848 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:21569298 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608893 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:18429043 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13516896 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608801 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14393520 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608755 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608864 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608793 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:18429043 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11601270 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608811 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11089997 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608874 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28899337 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689479 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608807 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:17850630 PMID:18429043 PMID:24033266 PMID:26467025 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608752 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:21436283 PMID:23804846 PMID:24033266 PMID:24875298 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608790 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608890 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608796 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:24875298 PMID:25468891 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608806 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:16679490 PMID:17850630 PMID:18348277 PMID:18429043 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608869 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:17850630 PMID:24033266 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608819 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:15660226 PMID:18429043 PMID:21569298 PMID:23591405 PMID:23757202 PMID:24033266 PMID:25741868 PMID:26467025 PMID:27884173 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608798 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:11138009 PMID:18429043 PMID:20146813 PMID:24033266 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608809 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:23804846 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11093700 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608898 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:18429043 PMID:20146813 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608799 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28907972 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:15660226 PMID:18273900 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608907 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:22607986 PMID:24033266 PMID:25741868 PMID:27068579 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608882 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:18429043 PMID:24033266 PMID:26264712 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608859 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38462333 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608797 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:18429043 PMID:24033266 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28908407 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26910596 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11608202 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:24618850 PMID:28492532 PMID:30245029


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15113979 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9690012 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608737 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608728 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16679490 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608905 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608804 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:17850630 PMID:18429043 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11600616 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608800 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608847 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:24033266 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608838 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16679490 PMID:17850630 PMID:20613545 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608896 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28906347 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608900 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:18429043 PMID:20146813 PMID:21569298 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9688985 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:18429043 PMID:24033266 PMID:28492532 PMID:30311386


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13705562 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30311386


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8606935 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:15660226 PMID:16679490 PMID:18429043 PMID:19683999 PMID:21078986 PMID:23208854 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532 PMID:29343940 PMID:30311386


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608826 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11096270 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:22135276 PMID:24033266 PMID:24767429 PMID:26969326 PMID:27792758 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608920 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608729 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25262649 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608823 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10053114 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28902900 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608766 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:18429043 PMID:23804846 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608844 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689470 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9692759 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608789 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:15660226 PMID:18429043 PMID:21569298 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608773 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608792 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:18429043 PMID:24033266 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608899 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:22135276 PMID:24033266 PMID:26467025 PMID:28492532 PMID:28912962


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608878 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28900366 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608886 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608884 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:18429043 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608930 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12905682 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28905550 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14708963 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38456047 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9693533 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8606931 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8606933 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:17850630 PMID:18429043 PMID:24033266 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608734 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10052339 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:17850630 PMID:2289998 PMID:22899989 PMID:24033266 PMID:25587757 PMID:25963016 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14692995 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:21940737 PMID:24033266 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15175573 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11601006 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11091451 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:16679490 PMID:16963483 PMID:19683999 PMID:20613545 PMID:21569298 PMID:21738395 PMID:24033266 PMID:25468891 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608940 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608785 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608840 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608894 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:20146813 PMID:24033266 PMID:25741868 PMID:26969326 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11092426 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:26969326 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8606932 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:16679490 PMID:19375528 PMID:20146813 PMID:21436283 PMID:22135276 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608743 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608758 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608828 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:17850630 PMID:18429043 PMID:20844544 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8606934 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:18429043 PMID:24033266 PMID:26467025 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10050380 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608768 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type I, French variety
  • Original References(s): PMID:24033266 PMID:26467025 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11093513 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38473919 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608919 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:17850630 PMID:24033266 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26894655 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608877 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:18429043 PMID:24033266 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608744 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:21073734 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608749 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8558369 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:17850630 PMID:22443853 PMID:22899989 PMID:23967202 PMID:24164807 PMID:24618850 PMID:24767429 PMID:25279224 PMID:25741868 PMID:25963016 PMID:26264712 PMID:26763877 PMID:27583405 PMID:27792758 PMID:28492532 PMID:30367262


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13540623 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608839 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11092174 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:24498627 PMID:25605338 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608747 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15125799 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608904 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9690455 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9692758 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9688438 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:24033266 PMID:25741868 PMID:26467025


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608927 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:24033266 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608787 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8642937 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26920203 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40905806 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691474 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608888 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608827 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608881 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:17850630 PMID:18429043 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15141357 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608921 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:17850630 PMID:18323324 PMID:24033266 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608771 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11602606 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26902040 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29148562


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608824 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608822 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15188526 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608760 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608759 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:17850630 PMID:18429043 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11599918 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9693604 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26969326 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15194090 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12900958 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28492532 PMID:31152317


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26915129 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13528816 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:15353998 PMID:18429043 PMID:19683999 PMID:23451239 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13532690 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:17850630 PMID:24033266 PMID:25472526 PMID:25741868 PMID:25963016 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11603524 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906811 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691475 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:18429043 PMID:24033266 PMID:25741868 PMID:28492532 PMID:31054281


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26905341 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608780 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608863 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:11857743 PMID:12075507 PMID:15353998 PMID:16679490 PMID:17407589 PMID:18429043 PMID:19683999 PMID:20513143 PMID:20613545 PMID:21436283 PMID:21569298 PMID:21940737 PMID:24033266 PMID:24498627 PMID:25404053 PMID:25741868 PMID:28492532 PMID:30303587


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11602635 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14393524 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:21940737 PMID:24033266 PMID:25231367 PMID:25404053 PMID:25425308 PMID:25741868 PMID:26969326 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608764 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:18429043 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10050519 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691072 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38468966 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689489 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608739 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608742 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608757 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11603481 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11600529 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8558363 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:12522556 PMID:15353998 PMID:21940737 PMID:24033266 PMID:25741868 PMID:2706105 PMID:27460420 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11096288 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11600888 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126730694 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532 PMID:30311386


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608805 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:11138009 PMID:16679490 PMID:21940737 PMID:24033266 PMID:25741868 PMID:27743452 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608723 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11599537 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11096217 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38496866 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:26445815 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8558357 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:11138009 PMID:12075507 PMID:18273900 PMID:18484607 PMID:20613545 PMID:21940737 PMID:24033266 PMID:25468891 PMID:25472526 PMID:25741868 PMID:26399936 PMID:26467025 PMID:28492532 PMID:30311386 PMID:32991204 PMID:35186827


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40905150 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906773 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26887691 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26917469 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38458785 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38495197 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38456968 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38462575 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532 PMID:30459346


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38466534 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:9536098


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13474561 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126732272 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15165302 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10053113 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26885005 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10050520 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:22135276 PMID:25741868 PMID:26969326 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38498297 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15128137 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13445799 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30311386


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906765 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13538456 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26898632 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13446241 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:18429043 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8558368 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:15537665 PMID:18273900 PMID:21228398 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38475776 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:26226137 PMID:28483220 PMID:28492532 PMID:28847902 PMID:30033219


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8642935 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38475047 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689476 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11088551 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26916179 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13537027 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40905146 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38496863 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:21404904 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:11138009 PMID:21940737 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906810 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type I, French variety
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9693536 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126737224 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38499240 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24416283 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40905815 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12791818 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:22899989 PMID:27460420 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11599950 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9687629 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532 PMID:30311386


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11607910 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40904679 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11665295 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26897184 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28492532 PMID:31152317


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40905808 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11599295 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:28492532 PMID:30733538


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691473 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:17576681 PMID:24033266 PMID:28492532 PMID:9536098


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11095768 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11634597 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10052928 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:16281288 PMID:17850630 PMID:18368581 PMID:25741868 PMID:27349180 PMID:28492532 PMID:29986705


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11600984 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608833 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11089503 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:21569298 PMID:25741868 PMID:25788563 PMID:28492532 PMID:35020051


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38494042 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:17576681 PMID:25741868 PMID:26467025 PMID:28492532 PMID:9536098


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608926 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40904675 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13541782 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28906016 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608761 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691490 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10051302 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13516345 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691470 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:26763877 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8558367 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:15537665 PMID:15660226 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10051820 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608891 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:17576681 PMID:22135276 PMID:24033266 PMID:25741868 PMID:28492532 PMID:35020051 PMID:36011334 PMID:9536098


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40887058 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30311386 PMID:34837038


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608851 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:11857743 PMID:17576681 PMID:21738395 PMID:25741868 PMID:28492532 PMID:9536098


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8558361 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:11090341 PMID:21940737 PMID:25741868 PMID:27018795 PMID:27792758 PMID:28492532 PMID:30303587 PMID:31445392 PMID:35020051


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11090753 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532 PMID:30311386 PMID:32467589


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608854 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608767 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:24767429 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608885 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:24033266 PMID:25741868


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11602193 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608721 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • 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 CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689487 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:23794683 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8558364 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12522556 PMID:19683999 PMID:25741868 PMID:28492532 PMID:35020051


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608939 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:11138009 PMID:21940737 PMID:24033266 PMID:25741868 PMID:28492532 PMID:33111992


  • An association has been curated linking CDH23 and Usher Syndrome Type 1B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26901388 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 16 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:21940737 PMID:25741868 PMID:28492532 PMID:29148562 PMID:30303587 PMID:32485727 PMID:32645618


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