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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking NLRC4 and hereditary spastic paraplegia 4 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:151741702 (Homo sapiens)
  • 25 RGD objects have been annotated to hereditary spastic paraplegia 4  (DOID:0110792)
  • 6 papers in RGD have been used to annotate NLRC4
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia 4
  • Original References(s): PMID:28492532


    • An association has been curated linking NLRC4 and hereditary spastic paraplegia 4 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:40903740 (Homo sapiens)
  • 25 RGD objects have been annotated to hereditary spastic paraplegia 4  (DOID:0110792)
  • 6 papers in RGD have been used to annotate NLRC4
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia 4
  • Original References(s): PMID:25741868


    • An association has been curated linking NLRC4 and hereditary spastic paraplegia 4 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:10766651|RGD:10766656|RGD:10766675|RGD:10766676 (Homo sapiens) & RGD:10766651|RGD:10766656|RGD:10766675|RGD:10766676 (Homo sapiens) & RGD:10766651|RGD:10766656|RGD:10766675|RGD:10766676 (Homo sapiens) & RGD:10766651|RGD:10766656|RGD:10766675|RGD:10766676 (Homo sapiens)
  • 25 RGD objects have been annotated to hereditary spastic paraplegia 4  (DOID:0110792)
  • 6 papers in RGD have been used to annotate NLRC4
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia 4
  • Original References(s): PMID:25065914


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