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GENE - TERM ANNOTATION REPORT

16 Annotations Found.

An association has been curated linking LMNA and autosomal recessive limb-girdle muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569615 (Homo sapiens)
  • 169 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy  (DOID:0110274)
  • 41 papers in RGD have been used to annotate LMNA
  • Curation Notes: ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive
  • Original References(s): PMID:12920062 PMID:18414213 PMID:18795223 PMID:19318026 PMID:19424285 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking LMNA and autosomal recessive limb-girdle muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10053441 (Homo sapiens)
  • 169 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy  (DOID:0110274)
  • 41 papers in RGD have been used to annotate LMNA
  • Curation Notes: ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive
  • Original References(s): PMID:17377071 PMID:18414213 PMID:18549403 PMID:19638735 PMID:24001739 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking LMNA and autosomal recessive limb-girdle muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610934 (Homo sapiens)
  • 169 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy  (DOID:0110274)
  • 41 papers in RGD have been used to annotate LMNA
  • Curation Notes: ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive
  • Original References(s): PMID:15475483 PMID:15998779 PMID:18414213 PMID:24033266 PMID:24721642 PMID:25741868 PMID:26467025 PMID:27896052 PMID:28492532 PMID:28785654


    • An association has been curated linking LMNA and autosomal recessive limb-girdle muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8622655 (Homo sapiens)
  • 169 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy  (DOID:0110274)
  • 41 papers in RGD have been used to annotate LMNA
  • Curation Notes: ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive
  • Original References(s): PMID:19427440 PMID:25741868 PMID:28492532


    • An association has been curated linking LMNA and autosomal recessive limb-girdle muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11644331 (Homo sapiens)
  • 169 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy  (DOID:0110274)
  • 41 papers in RGD have been used to annotate LMNA
  • Curation Notes: ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive
  • Original References(s): PMID:28492532


    • An association has been curated linking LMNA and autosomal recessive limb-girdle muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610948 (Homo sapiens)
  • 169 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy  (DOID:0110274)
  • 41 papers in RGD have been used to annotate LMNA
  • Curation Notes: ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive
  • Original References(s): PMID:18414213 PMID:19318026 PMID:24033266 PMID:24721642 PMID:25741868 PMID:28492532


    • An association has been curated linking LMNA and autosomal recessive limb-girdle muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610908 (Homo sapiens)
  • 169 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy  (DOID:0110274)
  • 41 papers in RGD have been used to annotate LMNA
  • Curation Notes: ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive
  • Original References(s): PMID:11102973 PMID:18414213 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532 PMID:29237675 PMID:29952368 PMID:32818388 PMID:33407844


    • An association has been curated linking LMNA and autosomal recessive limb-girdle muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11647082 (Homo sapiens)
  • 169 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy  (DOID:0110274)
  • 41 papers in RGD have been used to annotate LMNA
  • Curation Notes: ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive
  • Original References(s): PMID:11102973 PMID:25741868 PMID:29237675 PMID:29952368 PMID:32818388 PMID:33407844


    • An association has been curated linking LMNA and autosomal recessive limb-girdle muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11578013 (Homo sapiens)
  • 169 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy  (DOID:0110274)
  • 41 papers in RGD have been used to annotate LMNA
  • Curation Notes: ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:28679633 PMID:30402260 PMID:9536098


    • An association has been curated linking LMNA and autosomal recessive limb-girdle muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610909 (Homo sapiens)
  • 169 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy  (DOID:0110274)
  • 41 papers in RGD have been used to annotate LMNA
  • Curation Notes: ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive
  • Original References(s): PMID:11102973 PMID:24033266 PMID:25741868 PMID:28492532 PMID:29237675 PMID:29952368 PMID:32818388 PMID:33407844


    • An association has been curated linking LMNA and autosomal recessive limb-girdle muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569616 (Homo sapiens)
  • 169 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy  (DOID:0110274)
  • 41 papers in RGD have been used to annotate LMNA
  • Curation Notes: ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive
  • Original References(s): PMID:11102973 PMID:18414213 PMID:24033266 PMID:25741868 PMID:28492532 PMID:29237675 PMID:29952368 PMID:32818388 PMID:33407844


    • An association has been curated linking LMNA and autosomal recessive limb-girdle muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610913 (Homo sapiens)
  • 169 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy  (DOID:0110274)
  • 41 papers in RGD have been used to annotate LMNA
  • Curation Notes: ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:26602028 PMID:28492532


    • An association has been curated linking LMNA and autosomal recessive limb-girdle muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8610902|RGD:8610950 (Homo sapiens) & RGD:8610902|RGD:8610950 (Homo sapiens)
  • 169 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy  (DOID:0110274)
  • 41 papers in RGD have been used to annotate LMNA
  • Curation Notes: ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive
  • Original References(s): PMID:23861362 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking LMNA and autosomal recessive limb-girdle muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11585687|RGD:11645970 (Homo sapiens) & RGD:11585687|RGD:11645970 (Homo sapiens)
  • 169 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy  (DOID:0110274)
  • 41 papers in RGD have been used to annotate LMNA
  • Curation Notes: ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive
  • Original References(s): PMID:11102973 PMID:29237675 PMID:29952368 PMID:32818388 PMID:33407844


    • An association has been curated linking LMNA and autosomal recessive limb-girdle muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11583021|RGD:11583289|RGD:11644289|RGD:11644568|RGD:11644660|RGD:11644792|RGD:11645253|RGD:11645836|RGD:11647179|RGD:11647488|RGD:11649849|RGD:11665231 (Homo sapiens) & RGD:11583021|RGD:11583289|RGD:11644289|RGD:11644568|RGD:11644660|RGD:11644792|RGD:11645253|RGD:11645836|RGD:11647179|RGD:11647488|RGD:11649849|RGD:11665231 (Homo sapiens) & RGD:11583021|RGD:11583289|RGD:11644289|RGD:11644568|RGD:11644660|RGD:11644792|RGD:11645253|RGD:11645836|RGD:11647179|RGD:11647488|RGD:11649849|RGD:11665231 (Homo sapiens) & RGD:11583021|RGD:11583289|RGD:11644289|RGD:11644568|RGD:11644660|RGD:11644792|RGD:11645253|RGD:11645836|RGD:11647179|RGD:11647488|RGD:11649849|RGD:11665231 (Homo sapiens) & RGD:11583021|RGD:11583289|RGD:11644289|RGD:11644568|RGD:11644660|RGD:11644792|RGD:11645253|RGD:11645836|RGD:11647179|RGD:11647488|RGD:11649849|RGD:11665231 (Homo sapiens) & RGD:11583021|RGD:11583289|RGD:11644289|RGD:11644568|RGD:11644660|RGD:11644792|RGD:11645253|RGD:11645836|RGD:11647179|RGD:11647488|RGD:11649849|RGD:11665231 (Homo sapiens) & RGD:11583021|RGD:11583289|RGD:11644289|RGD:11644568|RGD:11644660|RGD:11644792|RGD:11645253|RGD:11645836|RGD:11647179|RGD:11647488|RGD:11649849|RGD:11665231 (Homo sapiens) & RGD:11583021|RGD:11583289|RGD:11644289|RGD:11644568|RGD:11644660|RGD:11644792|RGD:11645253|RGD:11645836|RGD:11647179|RGD:11647488|RGD:11649849|RGD:11665231 (Homo sapiens) & RGD:11583021|RGD:11583289|RGD:11644289|RGD:11644568|RGD:11644660|RGD:11644792|RGD:11645253|RGD:11645836|RGD:11647179|RGD:11647488|RGD:11649849|RGD:11665231 (Homo sapiens) & RGD:11583021|RGD:11583289|RGD:11644289|RGD:11644568|RGD:11644660|RGD:11644792|RGD:11645253|RGD:11645836|RGD:11647179|RGD:11647488|RGD:11649849|RGD:11665231 (Homo sapiens) & RGD:11583021|RGD:11583289|RGD:11644289|RGD:11644568|RGD:11644660|RGD:11644792|RGD:11645253|RGD:11645836|RGD:11647179|RGD:11647488|RGD:11649849|RGD:11665231 (Homo sapiens) & RGD:11583021|RGD:11583289|RGD:11644289|RGD:11644568|RGD:11644660|RGD:11644792|RGD:11645253|RGD:11645836|RGD:11647179|RGD:11647488|RGD:11649849|RGD:11665231 (Homo sapiens)
  • 169 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy  (DOID:0110274)
  • 41 papers in RGD have been used to annotate LMNA
  • Curation Notes: ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive


    • An association has been curated linking LMNA and autosomal recessive limb-girdle muscular dystrophy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11577521|RGD:11578589 (Homo sapiens) & RGD:11577521|RGD:11578589 (Homo sapiens)
  • 169 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy  (DOID:0110274)
  • 41 papers in RGD have been used to annotate LMNA
  • Curation Notes: ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive
  • Original References(s): PMID:25741868 PMID:28492532


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