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VARIANT - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking CV521122 and distal hereditary motor neuronopathy type 2D 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
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 2D  (DOID:0111210)
  • 0 papers in RGD have been used to annotate CV521122
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy 2D
  • Original References(s): PMID:28492532


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.