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1 Annotations Found.

An association has been curated linking RWDD1 and microcephaly 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:9831462 (Homo sapiens)
  • 238 RGD objects have been annotated to microcephaly  (DOID:10907)
  • 2 papers in RGD have been used to annotate RWDD1
  • Curation Notes: ClinVar Annotator: match by term: Microcephaly
  • Original References(s): PMID:24824130

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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.