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VARIANT - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking CV1910223 and Congenital Heart Defects, Multiple Types, 1, X-Linked 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
  • 13 RGD objects have been annotated to Congenital Heart Defects, Multiple Types, 1, X-Linked  (DOID:9003587)
  • 0 papers in RGD have been used to annotate CV1910223
  • Curation Notes: ClinVar Annotator: match by term: Heterotaxy, visceral, 1, X-linked
  • Original References(s): PMID:28492532


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