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1 Annotations Found.

An association has been curated linking CV786898 and X-linked severe combined immunodeficiency 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
  • 9 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 0 papers in RGD have been used to annotate CV786898
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:25741868 PMID:28492532

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