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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking LAMP2 and familial hypertrophic cardiomyopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11040026 (Homo sapiens)
  • 193 RGD objects have been annotated to familial hypertrophic cardiomyopathy  (DOID:0080326)
  • 19 papers in RGD have been used to annotate LAMP2
  • Curation Notes: ClinVar Annotator: match by term: Primary familial hypertrophic cardiomyopathy


  • An association has been curated linking LAMP2 and familial hypertrophic cardiomyopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569582 (Homo sapiens)
  • 193 RGD objects have been annotated to familial hypertrophic cardiomyopathy  (DOID:0080326)
  • 19 papers in RGD have been used to annotate LAMP2
  • Curation Notes: ClinVar Annotator: match by term: Primary familial hypertrophic cardiomyopathy
  • Original References(s): PMID:24033266


  • An association has been curated linking LAMP2 and familial hypertrophic cardiomyopathy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9832399 (Homo sapiens)
  • 193 RGD objects have been annotated to familial hypertrophic cardiomyopathy  (DOID:0080326)
  • 19 papers in RGD have been used to annotate LAMP2
  • Curation Notes: ClinVar Annotator: match by term: Primary familial hypertrophic cardiomyopathy
  • Original References(s): PMID:28492532


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