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1 Annotations Found.

An association has been curated linking Lmf2 and megaconial type congenital muscular dystrophy in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  • 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 from sequence orthology with LMF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to megaconial type congenital muscular dystrophy  (DOID:0110632)
  • 3 papers in RGD have been used to annotate Lmf2
  • Curation Notes: ClinVar Annotator: match by term: Megaconial type congenital muscular dystrophy
  • Original References(s): PMID:21665002 PMID:28005197 PMID:28492532 PMID:28902413

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