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GENE - TERM ANNOTATION REPORT

114 Annotations Found.

An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13791912 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11050310 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1D
  • Original References(s): PMID:26872967


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8558375 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:11398101 PMID:11487575 PMID:14570705 PMID:22981120 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13791388 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12739737 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38496761 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38460258 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:25741868


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38462838 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:25741868


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38461931 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:25741868


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38462868 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689666 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:24033266 PMID:25741868


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38461934 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:25741868


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11639605 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:24033266 PMID:24498627 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155736962 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9688942 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:11398101 PMID:11487575 PMID:14570705 PMID:16679490 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11599403 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:24033266 PMID:25468891 PMID:25741868 PMID:28492532 PMID:30311386


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126730706 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11603688 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8609347 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:15660226 PMID:24033266 PMID:25262649 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13782644 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13787483 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25307757 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152983190 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150447359 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11092506 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:24033266 PMID:25307757 PMID:25741868


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126914391 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26897449 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13787194 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:24831256 PMID:25999675 PMID:27610647 PMID:28492532 PMID:29625443


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13788183 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:24033266 PMID:27766948 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8609345 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:21569298 PMID:22815625 PMID:24033266 PMID:25468891 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11637425 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:27460420 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14705108 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28908875 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11603484 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8609354 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8558376 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:11398101 PMID:11487575 PMID:12711741 PMID:14570705 PMID:15028842 PMID:20301442 PMID:22815625 PMID:24033266 PMID:24105371 PMID:25262649 PMID:25307757 PMID:25525159 PMID:25741868 PMID:27460420 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13791180 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25307757 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40905090 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8609369 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:22135276 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8609306 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150410497 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11600960 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:30718709 PMID:9536098


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151887800 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:11398101 PMID:11487575 PMID:14570705 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8609309 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12892698 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26921799 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868 PMID:28281779 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155726221 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155735824 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155736801 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155737142 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155735934 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155735760 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155735680 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155735590 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155736449 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155729766 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155737045 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155737274 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155726806 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155728228 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155736176 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155729774 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155724004 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155729420 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155728425 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155728692 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155736714 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155735867 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155736149 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155729343 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155722587 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155726567 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155736846 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155723331 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155737047 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155735341 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9692099 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13783575 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868 PMID:28000701


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13536035 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8609311 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9688046 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126758840 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38465757 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:25741868


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155729418 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11647181 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13783193 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28905700 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:23967202 PMID:24164807 PMID:25741868 PMID:28492532 PMID:28847902 PMID:30245029


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26885955 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151779113 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38499919 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691059 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:23967202 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40905087 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15099593 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9688745 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:24033266 PMID:25307757 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26921729 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868 PMID:28281779 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8692320 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:15660226 PMID:22135276 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26904231 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126921502 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8609379 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38491221 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38461089 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126758842 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:17576681 PMID:22815625 PMID:23451239 PMID:25741868 PMID:28492532 PMID:9536098


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11088803 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155724993 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:11398101 PMID:11487575 PMID:14570705 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9688052 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127256131 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:11398101 PMID:11487575 PMID:14570705 PMID:16199547 PMID:18719945 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38491722 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868 PMID:28281779 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28905378 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868 PMID:27058588 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40904613 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11050318 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:11398101 PMID:11487575 PMID:14570705 PMID:16679490 PMID:18719945 PMID:21436283 PMID:21569298 PMID:24618850 PMID:25741868 PMID:26872967 PMID:28492532 PMID:29568747


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8609334 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:11398101 PMID:11487575 PMID:14570705 PMID:18484607 PMID:19375528 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred from experiment (EXP)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11089930 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26166082 PMID:28492532 PMID:34416374


  • An association has been curated linking PCDH15 and Usher syndrome type 1D in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155736912 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher syndrome type 1D  (DOID:0110831)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1D
  • Original References(s): PMID:11398101 PMID:11487575 PMID:14570705 PMID:28492532


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