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1 Annotations Found.

An association has been curated linking CV211373 and coenzyme Q10 deficiency disease 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
  • 38 RGD objects have been annotated to coenzyme Q10 deficiency disease  (DOID:0050730)
  • 0 papers in RGD have been used to annotate CV211373
  • Curation Notes: ClinVar Annotator: match by term: Coenzyme Q10 deficiency, Oculomotor Apraxia Type
  • Original References(s): PMID:24033266

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