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1 Annotations Found.

An association has been curated linking B3GALNT2 and congenital muscular dystrophy-dystroglycanopathy type A11 in Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with B3GALNT2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital muscular dystrophy-dystroglycanopathy type A11  (DOID:0111230)
  • 0 papers in RGD have been used to annotate B3GALNT2

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