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GENE - TERM ANNOTATION REPORT

4661 Annotations Found.

An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150541517 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151781898 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151892357 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151747064 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151790956 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151830449 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151797127 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151733671 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151831724 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:17259292 PMID:18055393 PMID:25007885 PMID:25640679 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151763928 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151784043 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151778701 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:20381484 PMID:23818053 PMID:25007885 PMID:25640679 PMID:28116794 PMID:28492532 PMID:28610567


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151882049 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13467747 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641723 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:26467025 PMID:7611292


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Malhotra SB, etal., Science. 1988 Nov 4;242(4879):755-9.
  • 2 additional annotations were made from Malhotra SB, etal., Science. 1988 Nov 4;242(4879):755-9.
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641722 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15144413 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14975522 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151846401 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151728979 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:25741868


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10049969 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151711053 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151887356 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:17259292 PMID:28492532 PMID:32403337


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10408934 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:10196701 PMID:26467025 PMID:28492532 PMID:9143930


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127314209 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10048372 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641753 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:14659407 PMID:19602481 PMID:23536893 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38461602 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151814252 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:15841391 PMID:16030524 PMID:16770791 PMID:21228398 PMID:22090376 PMID:25007885 PMID:27206868 PMID:28492532 PMID:9800909


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151801294 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151876368 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151892697 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151725879 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151825128 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151873655 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151789811 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127316076 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15144762 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12885324 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15118319 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151800088 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10049847 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13832871 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151840472 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:17576681 PMID:19230662 PMID:21515508 PMID:28492532 PMID:9536098


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151825945 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13515813 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151865774 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127314260 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151786796 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151786957 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151782583 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127299031 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151759374 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151852331 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:25640679 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151778471 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:12324874 PMID:15723292 PMID:28492532 PMID:8149204


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151838853 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641779 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150540849 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151877954 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38457514 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151808935 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151860665 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151716850 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151758455 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151856883 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151788689 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:18353051 PMID:22379338 PMID:22776072 PMID:28116794 PMID:28492532 PMID:28610567


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151860367 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16834926 PMID:19001018 PMID:19783145 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151814180 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151722485 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151748225 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151757319 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151865036 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151852382 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151846295 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151788594 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13592668 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy, pseudohypertrophic progressive, Duchenne type
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:21069337 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:25741868 PMID:28492532 PMID:31081998


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11640514 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13516467 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13464645 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151817917 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151878929 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Larcher T, etal., PLoS One. 2014 Oct 13;9(10):e110371. doi: 10.1371/journal.pone.0110371. eCollection 2014.
  • The annotation has been inferred from sequence orthology with Dmd (Rattus norvegicus) [(IMP) inferred from mutant phenotype]
  • 44 additional annotations were made from Larcher T, etal., PLoS One. 2014 Oct 13;9(10):e110371. doi: 10.1371/journal.pone.0110371. eCollection 2014.
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8562316 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532 PMID:7951253


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151874529 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151739056 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126923605 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:21073564 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:27593222 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151778620 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126908173 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151742175 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11560203 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532 PMID:31081998 PMID:7849724


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126923137 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126914142 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38492899 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126919995 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126921420 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126920433 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126924404 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126923682 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126919276 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151762203 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16917894 PMID:18752307 PMID:2063877 PMID:2316519 PMID:25640679 PMID:26911353 PMID:28492532 PMID:8034300 PMID:9441825


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126921234 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126922762 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126915602 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126922413 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126915132 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126917440 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13802941 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:9536098


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Deconinck AE, etal., Cell 1997 Aug 22;90(4):717-27.
  • The annotation has been inferred from sequence orthology with Dmd (Mus musculus) [(IGI) inferred from genetic interaction]
  • 5 additional annotations were made from Deconinck AE, etal., Cell 1997 Aug 22;90(4):717-27.
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126922441 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28880319 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126920209 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126922576 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126908485 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126913831 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126922981 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126917156 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126917592 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126916842 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126917842 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:21515508 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12912767 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126918669 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126916527 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126922179 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126920215 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126924155 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126923480 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151788251 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:10612827 PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151784859 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:17259292 PMID:19309270 PMID:25007885 PMID:25640679 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151719768 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:18054699 PMID:25937795 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151847871 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126921530 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150540829 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126917599 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126911819 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126917756 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8562305 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13490725 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126917840 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:25640679 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11636257 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12854332 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13466446 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13523156 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13498373 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151831478 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13478859 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151888820 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred from direct assay (IDA)
  •  
  • The annotation was made from Flanigan KM, etal., Hum Gene Ther. 2013 Sep;24(9):797-806. doi: 10.1089/hum.2013.092.
  • 2 additional annotations were made from Flanigan KM, etal., Hum Gene Ther. 2013 Sep;24(9):797-806. doi: 10.1089/hum.2013.092.
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Qualifier: treatment


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38475301 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151804405 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16199547 PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13511840 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12742876 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15140127 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15107819 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26885015 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26894174 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:12754415 PMID:28492532 PMID:9007319


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15103974 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38461375 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13467821 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15100467 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13511471 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13540585 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:15723292 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38493155 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38469141 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15157869 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151790287 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38495764 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12839950 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38470678 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13510663 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15102850 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13524027 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10408891 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:19937601 PMID:26467025


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38481072 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532 PMID:31081998


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13499802 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26894261 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:12111668 PMID:25076844 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15161405 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151865962 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15132640 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151860892 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151853119 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16199547 PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15151071 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15098741 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12880597 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151784940 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:18353051 PMID:22379338 PMID:28116794 PMID:28492532 PMID:28610567


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38476869 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127326283 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127301134 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15101923 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151720391 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:18055393 PMID:26081009 PMID:28492532 PMID:31705731


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13833131 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127312515 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15124397 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10408903 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:12632325 PMID:16770791 PMID:19937601 PMID:20485447 PMID:21972111 PMID:25007885 PMID:26467025 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127314404 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127286491 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127286407 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127324308 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11636429 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:19959795 PMID:26467025 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15120510 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11577583 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127326288 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38493340 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127324281 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127321288 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13528127 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151841166 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15098146 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15125623 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151837239 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151851439 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:25640679 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13497897 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127310784 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:21404198 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:25741868


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14704430 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8562278 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:7951253


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127313423 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15097601 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15127367 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15113962 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14743964 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:21404201 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:25741868


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15119999 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127316322 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10408927 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:17259292 PMID:26467025


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127313655 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127310508 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38493276 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150541544 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127311338 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15139406 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127295137 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14704433 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11633271 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy, pseudohypertrophic progressive, Duchenne type
  • Original References(s): PMID:17041906 PMID:21969337 PMID:25741868 PMID:28492532 PMID:7581396


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127295605 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Miller G, etal., Hum Mol Genet. 2012 Oct 15;21(20):4508-20. Epub 2012 Jul 18.
  • The annotation has been inferred from sequence orthology with Dmd (Mus musculus) [(IMP) inferred from mutant phenotype]
  • 2 additional annotations were made from Miller G, etal., Hum Mol Genet. 2012 Oct 15;21(20):4508-20. Epub 2012 Jul 18.
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127321589 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:41406503 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:26467025 PMID:26743743 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127320390 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127322183 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38472745 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38466475 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15177052 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15115088 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127319467 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127310459 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15112008 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127290037 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15134160 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151763923 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15113699 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127310648 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151768134 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151828538 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151826989 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127311941 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127299869 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13612038 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151856440 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127310603 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127322224 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15155000 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127324849 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13479876 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:19449031 PMID:2063877 PMID:21851881 PMID:22090376 PMID:24217213 PMID:25244321 PMID:26081009 PMID:26911353 PMID:28492532 PMID:8423832


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15129267 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:34890818 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:25741868 PMID:28492532 PMID:32860008


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127304694 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641588 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127314323 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13612233 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:17253928 PMID:25972034 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151852305 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127276757 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127295697 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15117262 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641533 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127315032 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15196072 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13523435 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127314896 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127302707 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15103359 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26915348 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:17726484 PMID:19959795 PMID:26911353 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11642054 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641553 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15130508 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641519 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13611946 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15114476 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26916492 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Dystrophinopathies
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15117031 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151725719 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15127674 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14394116 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641713 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10052039 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127245359 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13611874 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13611855 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641665 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641595 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:11524473 PMID:24033266 PMID:26467025 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26896600 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532 PMID:8034300


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13612073 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15143322 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13837875 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13499742 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127317969 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13834722 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641672 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12884381 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13834440 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15143258 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38460371 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127303127 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13611894 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127290929 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13529181 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13523237 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641770 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641444 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy, pseudohypertrophic progressive, Duchenne type
  • Original References(s): PMID:19937601 PMID:24033266 PMID:25741868 PMID:26284620 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151838854 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151862256 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151750080 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127306305 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127291024 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151869160 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532 PMID:30833962


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13835447 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151859152 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127301425 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151760597 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:16834926 PMID:19602481 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15135152 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38486356 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127290528 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38493728 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38481069 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641760 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:23757202 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13499066 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127303489 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15102545 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12840785 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127311518 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127295725 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127295271 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127311660 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15189155 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127314287 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:21404199 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:25741868


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15195887 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38483699 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127314616 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057432 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151719810 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127297654 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641362 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127308522 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15118759 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641392 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:23757202 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15139144 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15111601 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13494402 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:10392746 PMID:16917894 PMID:28492532 PMID:9800909


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127300069 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15182809 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26897558 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127309226 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127301935 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15196179 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641411 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13611987 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641529 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127304858 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151858162 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:25076844 PMID:28492532 PMID:9800909


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15114863 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127307930 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127318044 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13611936 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:25244321 PMID:27593222 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151760888 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38468959 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127306161 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641456 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26886124 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641527 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13516106 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28875780 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641548 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15143822 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15149231 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127308566 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15174940 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15180386 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127325680 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127325700 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127290700 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127296505 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13481178 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8637844 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11643020 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15186616 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15197571 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127290040 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641571 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8562336 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:17024373


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127278147 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127278148 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13836331 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127269773 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:22894145 PMID:28492532 PMID:31705731


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38467969 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641573 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:23757202 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13501036 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13528694 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10052879 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11349874 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28888464 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151710148 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:15528988 PMID:21515508 PMID:28492532 PMID:31705731


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13479364 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26896998 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:19367636 PMID:20153965 PMID:28492532 PMID:9007319


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15130522 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38480965 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057431 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Muscular dystrophy, pseudohypertrophic progressive, Duchenne type
  • Original References(s): PMID:19760747 PMID:24033266 PMID:25007885 PMID:25741868 PMID:28492532 PMID:7849724


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641458 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641657 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:19937601 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057435 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:25741868 PMID:28492532 PMID:31333075 PMID:31568572


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127246090 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:19937601 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38475632 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14701437 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:15684864 PMID:15723292 PMID:25482253 PMID:28116794 PMID:28492532 PMID:28610567


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13483686 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12883101 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12882202 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13499641 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38498270 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40889413 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:25741868


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127322121 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641692 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:23757202 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641699 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150540402 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127314256 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641683 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14394121 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127311734 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38484192 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14718660 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:11257468 PMID:16030524 PMID:18261911 PMID:18752307 PMID:20683981 PMID:22090376 PMID:26911353 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641345 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151807248 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15110379 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127306159 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641728 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13612257 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641721 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127306628 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127307019 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127292325 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15140670 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12839266 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641504 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127306612 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127288843 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15197764 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15151105 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10052628 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13611837 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26901613 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150541205 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:14695533 PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151858089 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127293335 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127292761 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127312923 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151813471 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38469505 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127318919 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127306721 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Dystrophinopathies
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:21073452 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641516 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151850227 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13468153 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38475343 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38473534 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15153225 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127233786 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15151509 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15181889 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40903356 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:25741868 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127269771 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13835358 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26899740 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26899787 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:11524473 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15108794 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15106738 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127270733 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16030524 PMID:16770791 PMID:28116794 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127313582 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151777120 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15117595 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127269763 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:17259292 PMID:1864612 PMID:28492532 PMID:8543940


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057437 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127288005 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151890998 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13835708 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12886534 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38484609 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127311454 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38479307 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38463974 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127332394 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641572 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:19937601 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532 PMID:30086531


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641558 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:19937601 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15124158 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8562309 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:7951253


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127305821 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127307209 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13503610 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127306640 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15195179 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14734869 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641534 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38482344 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:26934379 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151750463 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16030524 PMID:16770791 PMID:16917894 PMID:25007885 PMID:25640679 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12839242 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26919145 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641618 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127277582 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151760089 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13838439 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151878505 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13497800 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38481472 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11642546 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151836815 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151817094 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151768958 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127313771 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26896701 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16049303 PMID:19367636 PMID:19937601 PMID:28492532 PMID:28503591 PMID:9628192


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15123077 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11093660 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641591 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10053212 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38492317 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127329252 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12842214 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13464881 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10408924 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:17041906 PMID:26467025


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11643188 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15171298 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10045025 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38481558 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12881814 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641606 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641658 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641663 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641603 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641593 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13836629 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12891664 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641687 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11643526 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14701335 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:18353051 PMID:28492532 PMID:8413368


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127314935 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26893470 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:2063877 PMID:25482253 PMID:28492532 PMID:9007319


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13612236 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16030524 PMID:18752307 PMID:25482253 PMID:28492532 PMID:9800909


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12890773 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15100837 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15156517 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15145000 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13612162 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151872577 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641694 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:21520333 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15142732 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641681 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8641700 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:19937601 PMID:24033266 PMID:26467025 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:25317776 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:16770791 PMID:25007885 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151764057 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15191701 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127276255 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328648 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15123221 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15142194 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151727827 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:25741868


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127336163 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14701789 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:15655674 PMID:18752307 PMID:21520333 PMID:21896784 PMID:24099565 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151854413 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12880519 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151877060 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15143178 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151785006 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:17259292 PMID:19937601 PMID:25482253 PMID:25640679 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15194440 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127337869 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127303264 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127276913 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127315001 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13516188 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13498929 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14718239 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:11257468 PMID:16030524 PMID:18261911 PMID:18752307 PMID:20683981 PMID:22090376 PMID:26911353 PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12886402 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15115146 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15101960 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127321037 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127268379 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12882186 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15136274 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328442 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15109345 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26910329 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127302131 (Homo sapiens)
  • 34 RGD objects have been annotated to Duchenne muscular dystrophy  (DOID:11723)
  • 26 papers in RGD have been used to annotate DMD
  • Curation Notes: ClinVar Annotator: match by term: Duchenne muscular dystrophy
  • Original References(s): PMID:28492532


  • An association has been curated linking DMD and Duchenne muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11637301 (Homo sapiens)
  • 34 RGD objects have been an