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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking MYH8 and congenital myopathy 6 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
  • The annotation has been inferred by association of genotype and phenotype with RGD:26897810 (Homo sapiens)
  • 15 RGD objects have been annotated to congenital myopathy 6  (DOID:0080719)
  • 9 papers in RGD have been used to annotate MYH8
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, proximal, and ophthalmoplegia
  • Original References(s): PMID:28492532


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