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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking WFDC1 and persistent fetal circulation 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
  • The annotation has been inferred by association of genotype and phenotype with RGD:38597515 (Homo sapiens)
  • 44 RGD objects have been annotated to persistent fetal circulation syndrome  (DOID:13042)
  • 5 papers in RGD have been used to annotate WFDC1
  • Curation Notes: ClinVar Annotator: match by term: Congenital alveolar capillary dysplasia


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