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VARIANT - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking CV577721 and familial hemiplegic migraine 1 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
  • 11 RGD objects have been annotated to familial hemiplegic migraine 1  (DOID:0111181)
  • 0 papers in RGD have been used to annotate CV577721
  • Curation Notes: ClinVar Annotator: match by term: Migraine, familial hemiplegic, 1
  • Original References(s): PMID:10371528 PMID:16043807 PMID:16199547 PMID:19486177 PMID:25735478 PMID:25741868 PMID:26467025 PMID:26912519 PMID:27250579 PMID:28492532 PMID:31506931 PMID:33144682 PMID:36530930


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