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1 Annotations Found.

An association has been curated linking Fgf8 and Kallmann Syndrome 6 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 FGF8 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Kallmann Syndrome 6  (DOID:9008142)
  • 26 papers in RGD have been used to annotate Fgf8
  • Curation Notes: ClinVar Annotator: match by term: Kallmann syndrome 6
  • Original References(s): PMID:22399515 PMID:23533228 PMID:25131394 PMID:25741868 PMID:26467025 PMID:26857713 PMID:28492532 PMID:29584859

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