Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

70 Annotations Found.

An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10052799 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: HEARING LOSS, PROGRESSIVE, WITH OPTIC ATROPHY AND/OR IMPAIRED GLUCOSE REGULATION
  • Original References(s): PMID:18544103 PMID:24033266 PMID:25133958 PMID:25741868 PMID:28492532


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156363628 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:15277431 PMID:23981289 PMID:25741868 PMID:28492532 PMID:31850070 PMID:32938580 PMID:9817917


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10409778 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: HEARING LOSS, PROGRESSIVE, WITH OPTIC ATROPHY AND/OR IMPAIRED GLUCOSE REGULATION
  • Original References(s): PMID:25741868 PMID:26284228 PMID:28492532 PMID:31264968


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12906981 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:12754709 PMID:15277431 PMID:25741868 PMID:28492532 PMID:31567480


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689741 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: HEARING LOSS, PROGRESSIVE, WITH OPTIC ATROPHY AND/OR IMPAIRED GLUCOSE REGULATION
  • Original References(s): PMID:10679252 PMID:24033266 PMID:25388789 PMID:25741868 PMID:28492532


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8602255 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:21538838


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13832592 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11093222 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: HEARING LOSS, PROGRESSIVE, WITH OPTIC ATROPHY AND/OR IMPAIRED GLUCOSE REGULATION
  • Original References(s): PMID:19877185 PMID:20069065 PMID:24033266


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9690350 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:12955714 PMID:17603484 PMID:18060660 PMID:20301750 PMID:20738327 PMID:24033266 PMID:25741868 PMID:28492532 PMID:33879153


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10409206 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: HEARING LOSS, PROGRESSIVE, WITH OPTIC ATROPHY AND/OR IMPAIRED GLUCOSE REGULATION
  • Original References(s): PMID:15605410 PMID:24033266 PMID:25741868 PMID:28492532 PMID:30311386


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608320 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:11709537 PMID:12955714 PMID:17603484 PMID:18060660 PMID:20301750 PMID:20738327 PMID:24033266 PMID:25133958 PMID:25262649 PMID:25741868 PMID:28492532 PMID:33879153


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8602254 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:11295831 PMID:19877185 PMID:20875904 PMID:21067485 PMID:21143470 PMID:21538838 PMID:22238590 PMID:24033266 PMID:24890733 PMID:25741868 PMID:26435059 PMID:26467025 PMID:26875006 PMID:27395765 PMID:28432734 PMID:28492532 PMID:29529044


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10411594 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:24890733 PMID:25211237 PMID:25741868 PMID:27217304 PMID:28468959 PMID:32219690


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28903409 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29563951


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28900492 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:12955714 PMID:17603484 PMID:18060660 PMID:20301750 PMID:20738327 PMID:25741868 PMID:28492532 PMID:33879153


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38598471 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:12955714 PMID:17603484 PMID:18060660 PMID:20301750 PMID:20738327 PMID:25741868 PMID:33879153


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:153347036 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:25741868


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11584274 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:12955714 PMID:17603484 PMID:18060660 PMID:20301750 PMID:20738327 PMID:25741868 PMID:28492532 PMID:33879153


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151350434 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:25741868


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151236084 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13216274 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:10521293 PMID:16806192 PMID:25741868 PMID:28432734 PMID:28492532 PMID:30773290


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28888518 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:15234338 PMID:25741868 PMID:27911912 PMID:28492532


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10410871 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: HEARING LOSS, PROGRESSIVE, WITH OPTIC ATROPHY AND/OR IMPAIRED GLUCOSE REGULATION
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8691655 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:10679252 PMID:12955714 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8691647 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: HEARING LOSS, PROGRESSIVE, WITH OPTIC ATROPHY AND/OR IMPAIRED GLUCOSE REGULATION
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10410478 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:25048417 PMID:25741868 PMID:28492532 PMID:30311386


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151235408 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:28492532


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11586110 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:12955714 PMID:23981289 PMID:24890733 PMID:25741868 PMID:26025012 PMID:28492532 PMID:28559085


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11584690 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8596469 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:16648378 PMID:17492394 PMID:18544103 PMID:20301750 PMID:21917145 PMID:24033266 PMID:25741868 PMID:26346818 PMID:28492532 PMID:29529044 PMID:30311386 PMID:32567228


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608303 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:11920861 PMID:12955714 PMID:24033266 PMID:25133958 PMID:25741868 PMID:28492532


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10411228 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:10521293 PMID:15277431 PMID:16151413 PMID:19042979 PMID:21067485 PMID:21446023 PMID:21538838 PMID:21602428 PMID:23429432 PMID:24033266 PMID:25741868 PMID:27617222 PMID:28492532 PMID:31600780


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608330 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:18414213 PMID:24033266 PMID:25741868 PMID:28492532 PMID:29632382


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10410632 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:19292454 PMID:20738327 PMID:24033266 PMID:25741868 PMID:27617222 PMID:28492532


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10409554 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:12955714 PMID:17603484 PMID:18060660 PMID:20301750 PMID:20738327 PMID:24033266 PMID:25741868 PMID:28492532 PMID:33879153


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28900039 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:12955714 PMID:17603484 PMID:18060660 PMID:20301750 PMID:20738327 PMID:25741868 PMID:28492532 PMID:33879153


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151236141 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:12955714 PMID:17603484 PMID:18060660 PMID:20301750 PMID:20738327 PMID:33879153


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:21071291 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:12955714 PMID:17603484 PMID:18060660 PMID:19042979 PMID:20301750 PMID:20738327 PMID:24890733 PMID:25741868 PMID:28492532 PMID:28802351 PMID:31313226 PMID:33879153


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608315 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:12955714 PMID:17603484 PMID:18060660 PMID:20301750 PMID:20738327 PMID:24033266 PMID:25741868 PMID:28492532 PMID:33879153


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11588619 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:25741868


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9688300 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:12955714 PMID:17603484 PMID:18060660 PMID:20301750 PMID:20738327 PMID:24033266 PMID:25741868 PMID:28492532 PMID:33879153


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689796 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:11244483 PMID:12955714 PMID:15234338 PMID:15473915 PMID:17492394 PMID:24033266 PMID:25741868 PMID:28492532 PMID:29529044


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10053240 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: HEARING LOSS, PROGRESSIVE, WITH OPTIC ATROPHY AND/OR IMPAIRED GLUCOSE REGULATION
  • Original References(s): PMID:12955714 PMID:17603484 PMID:18060660 PMID:20301750 PMID:20738327 PMID:25741868 PMID:26969326 PMID:28492532 PMID:30311386 PMID:33046911 PMID:33879153


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28892643 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:12955714 PMID:17603484 PMID:18060660 PMID:20301750 PMID:20738327 PMID:25741868 PMID:28492532 PMID:33879153


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8691651 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:12955714 PMID:17603484 PMID:18060660 PMID:20301750 PMID:20738327 PMID:24033266 PMID:25741868 PMID:28492532 PMID:33879153


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8642240 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:11709538 PMID:11920861 PMID:12107816 PMID:15473915 PMID:15605410 PMID:18544103 PMID:20875904 PMID:24033266 PMID:24909696 PMID:25741868 PMID:25895475 PMID:26467025 PMID:28492532 PMID:34746052


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689731 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28898002 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:25741868


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126740739 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689795 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:11916957 PMID:12073007 PMID:12955714 PMID:20028947 PMID:24033266 PMID:25262649 PMID:25497598 PMID:25741868 PMID:28492532


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608329 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:12955714 PMID:17603484 PMID:18060660 PMID:20301750 PMID:20738327 PMID:24033266 PMID:25741868 PMID:28492532 PMID:33879153


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:42723713 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: HEARING LOSS, PROGRESSIVE, WITH OPTIC ATROPHY AND/OR IMPAIRED GLUCOSE REGULATION
  • Original References(s): PMID:12955714 PMID:17603484 PMID:18060660 PMID:20301750 PMID:20738327 PMID:33879153


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10411064 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: HEARING LOSS, PROGRESSIVE, WITH OPTIC ATROPHY AND/OR IMPAIRED GLUCOSE REGULATION
  • Original References(s): PMID:24033266 PMID:25133958 PMID:25741868 PMID:28492532 PMID:30180840


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10410770 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:25741868 PMID:27068579 PMID:28492532


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10409128 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:15277431 PMID:23981289 PMID:25741868 PMID:28492532


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28892096 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:25741868 PMID:28492532 PMID:33841295


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8596472 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:15912360 PMID:18688868 PMID:25741868 PMID:28492532


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome 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
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13836661 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11640498 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:11295831 PMID:25741868 PMID:28492532 PMID:31264968


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151883751 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:23373429 PMID:25741868 PMID:25895475 PMID:28432734 PMID:28492532 PMID:32350710 PMID:33980734 PMID:35602877 PMID:9771706


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10042537 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: HEARING LOSS, PROGRESSIVE, WITH OPTIC ATROPHY AND/OR IMPAIRED GLUCOSE REGULATION
  • Original References(s): PMID:12955714 PMID:17603484 PMID:18040659 PMID:20028947 PMID:24033266 PMID:25714468 PMID:25741868 PMID:27167055 PMID:28492532 PMID:30245029 PMID:31521625 PMID:31980526 PMID:34356170 PMID:34556497 PMID:35206658 PMID:36208030 PMID:9856492


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151831092 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10409290 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:12955714 PMID:17603484 PMID:18060660 PMID:20301750 PMID:20738327 PMID:25741868 PMID:28492532 PMID:33879153


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151846225 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150541930 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:25741868 PMID:28492532 PMID:33841295


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12738945 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: HEARING LOSS, PROGRESSIVE, WITH OPTIC ATROPHY AND/OR IMPAIRED GLUCOSE REGULATION
  • Original References(s): PMID:25741868 PMID:26435059 PMID:27959697 PMID:28492532 PMID:31264968


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10411156 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:25741868 PMID:26435059 PMID:26969326 PMID:28492532 PMID:29529044 PMID:32883240 PMID:36597107 PMID:36729443


  • An association has been curated linking WFS1 and autosomal dominant Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11585272 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal dominant Wolfram syndrome  (DOID:0080584)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram-like syndrome, autosomal dominant
  • Original References(s): PMID:25741868 PMID:28492532


  • Go Back to source page   Continue to Ontology report