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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking EDN1 and Auriculocondylar Syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8591075 (Homo sapiens)
  • 1 RGD objects have been annotated to Auriculocondylar Syndrome 3  (DOID:9002646)
  • 126 papers in RGD have been used to annotate EDN1
  • Curation Notes: ClinVar Annotator: match by term: Auriculocondylar syndrome 3
  • Original References(s): PMID:23315542 PMID:24268655


    • An association has been curated linking EDN1 and Auriculocondylar Syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8591076 (Homo sapiens)
  • 1 RGD objects have been annotated to Auriculocondylar Syndrome 3  (DOID:9002646)
  • 126 papers in RGD have been used to annotate EDN1
  • Curation Notes: ClinVar Annotator: match by term: Auriculocondylar syndrome 3
  • Original References(s): PMID:12244558 PMID:24268655


    • An association has been curated linking EDN1 and Auriculocondylar Syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to Auriculocondylar Syndrome 3  (DOID:9002646)
  • 126 papers in RGD have been used to annotate EDN1


    • An association has been curated linking EDN1 and Auriculocondylar Syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8600290 (Homo sapiens)
  • 1 RGD objects have been annotated to Auriculocondylar Syndrome 3  (DOID:9002646)
  • 126 papers in RGD have been used to annotate EDN1
  • Curation Notes: ClinVar Annotator: match by term: Auriculocondylar syndrome 3
  • Original References(s): PMID:17357073 PMID:18288492 PMID:25741868 PMID:28492532


    • An association has been curated linking EDN1 and Auriculocondylar Syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150512221 (Homo sapiens)
  • 1 RGD objects have been annotated to Auriculocondylar Syndrome 3  (DOID:9002646)
  • 126 papers in RGD have been used to annotate EDN1
  • Curation Notes: ClinVar Annotator: match by term: Auriculocondylar syndrome 3
  • Original References(s): PMID:25741868 PMID:28492532


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