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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking EDARADD and ectodermal dysplasia 10B in Homo sapiens.        

  • The association was inferred from experiment (EXP)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 15 RGD objects have been annotated to ectodermal dysplasia 10B  (DOID:0111665)
  • 7 papers in RGD have been used to annotate EDARADD
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking EDARADD and ectodermal dysplasia 10B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28887322|RGD:28897162 (Homo sapiens) & RGD:28887322|RGD:28897162 (Homo sapiens)
  • 15 RGD objects have been annotated to ectodermal dysplasia 10B  (DOID:0111665)
  • 7 papers in RGD have been used to annotate EDARADD
  • Curation Notes: ClinVar Annotator: match by term: Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive


    • An association has been curated linking EDARADD and ectodermal dysplasia 10B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11584797|RGD:11595306|RGD:28887683 (Homo sapiens) & RGD:11584797|RGD:11595306|RGD:28887683 (Homo sapiens) & RGD:11584797|RGD:11595306|RGD:28887683 (Homo sapiens)
  • 15 RGD objects have been annotated to ectodermal dysplasia 10B  (DOID:0111665)
  • 7 papers in RGD have been used to annotate EDARADD
  • Curation Notes: ClinVar Annotator: match by term: Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive
  • Original References(s): PMID:25741868


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