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1 Annotations Found.

An association has been curated linking CV318973 and congenital disorder of glycosylation 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
  • 148 CRRD objects have been annotated to congenital disorder of glycosylation  (DOID:5212)
  • 0 papers in CRRD have been used to annotate CV318973
  • Curation Notes: ClinVar Annotator: match by term: Congenital disorder of glycosylation
  • Original References(s): PMID:28492532

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