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GENE - TERM ANNOTATION REPORT

64 Annotations Found.

An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8595368 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Deafness, mitochondrial, modifier of
  • Original References(s): PMID:25741868 PMID:28049726 PMID:28492532 PMID:8817331


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152109252 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8691451 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949328 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8602333 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:19732863 PMID:21931168 PMID:23625533 PMID:25665837 PMID:25741868 PMID:28492532 PMID:31160058


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127251063 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:16199547 PMID:19732863 PMID:23625533 PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11617731 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151797583 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:19732863 PMID:23625533 PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127244403 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:19732863 PMID:23625533 PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13786818 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:19732863 PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13836980 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:19732863 PMID:23625533 PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28873309 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151890759 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:16199547 PMID:19732863 PMID:23625533 PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151825865 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:16199547 PMID:19732863 PMID:23625533 PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949339 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949351 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness 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
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151869954 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:19732863 PMID:23625533 PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949354 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14704214 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:16199547 PMID:19732863 PMID:23625533 PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12906589 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:17576681 PMID:21931168 PMID:25741868 PMID:28492532 PMID:9536098


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127260988 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:19732863 PMID:23625533 PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949327 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949353 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949342 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949355 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151881866 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:16199547 PMID:19732863 PMID:23625533 PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949343 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949329 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38465262 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868 PMID:28492532 PMID:28973083 PMID:30740308 PMID:33365252 PMID:33485800 PMID:36305855


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26903090 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:19732863 PMID:23625533 PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13791680 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:21153446 PMID:21169334 PMID:25741868 PMID:28492532 PMID:30369941 PMID:33365252


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949345 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949356 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949330 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949349 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949341 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10409960 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868 PMID:26633542 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949331 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949336 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156316149 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:19732863 PMID:23625533 PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156402672 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:19732863 PMID:23625533 PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38471100 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:19732863 PMID:23625533 PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156189279 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:16199547 PMID:19732863 PMID:23625533 PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14709656 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:16199547 PMID:19732863 PMID:23625533 PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155266544 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949352 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26892312 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:19732863 PMID:23625533 PMID:25741868 PMID:28492532 PMID:30740308


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127250811 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:16199547 PMID:19732863 PMID:23625533 PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8595369 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:19732863 PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949332 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949338 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156399042 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:19732863 PMID:23625533 PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401868128 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949346 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949337 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28885645 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868 PMID:28492532 PMID:33485800


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949333 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10411490 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:19732863 PMID:23625533 PMID:25741868 PMID:26633542 PMID:28252636 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949335 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14693242 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:19732863 PMID:23625533 PMID:25741868 PMID:28492532


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401949347 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMU and aminoglycoside-induced deafness in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13790350 (Homo sapiens)
  • 5 RGD objects have been annotated to aminoglycoside-induced deafness  (DOID:0111734)
  • 7 papers in RGD have been used to annotate TRMU
  • Curation Notes: ClinVar Annotator: match by term: Aminoglycoside-induced deafness
  • Original References(s): PMID:19732863 PMID:23625533 PMID:25741868 PMID:28492532


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