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1 Annotations Found.

An association has been curated linking Rapsn and congenital disorder of glycosylation type IIc in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  • 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 from sequence orthology with RAPSN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 41 RGD objects have been annotated to congenital disorder of glycosylation type IIc  (DOID:0070255)
  • 9 papers in RGD have been used to annotate Rapsn
  • Curation Notes: ClinVar Annotator: match by term: Rambam Hasharon syndrome
  • Original References(s): PMID:28492532

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