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VARIANT - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking CV29873 and Retinal dystrophy 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
  • 586 RGD objects have been annotated to Retinal dystrophy  (HP:0000556)
  • 1 papers in RGD have been used to annotate CV29873
  • Curation Notes: ClinVar Annotator: match by term: Retinal dystrophy
  • Original References(s): PMID:11875050 PMID:15851576 PMID:15882147 PMID:16671097 PMID:21791244 PMID:25741868 PMID:28492532 PMID:28945494


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