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VARIANT - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking CV1021691 and congenital disorder of glycosylation type IIg 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
  • 6 RGD objects have been annotated to congenital disorder of glycosylation type IIg  (DOID:0070259)
  • 0 papers in RGD have been used to annotate CV1021691
  • Curation Notes: ClinVar Annotator: match by term: Congenital disorder of glycosylation type 2G
  • Original References(s): PMID:25741868


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