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VARIANT - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking CV77926 and Romano-Ward Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • 22 RGD objects have been annotated to Romano-Ward Syndrome  (DOID:9004730)
  • 1 papers in RGD have been used to annotate CV77926
  • Curation Notes: ClinVar Annotator: match by term: Romano-Ward syndrome
  • Original References(s): PMID:19841300 PMID:22581653 PMID:25649125 PMID:25741868 PMID:25854863 PMID:26318259 PMID:28492532 PMID:29197658 PMID:31696929


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