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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking CCDC22 and immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome 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:151800854 (Homo sapiens)
  • 92 RGD objects have been annotated to immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome  (DOID:0090110)
  • 5 papers in RGD have been used to annotate CCDC22
  • Curation Notes: ClinVar Annotator: match by term: Insulin-dependent diabetes mellitus secretory diarrhea syndrome
  • Original References(s): PMID:28492532


    • An association has been curated linking CCDC22 and immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome 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:156445719 (Homo sapiens)
  • 92 RGD objects have been annotated to immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome  (DOID:0090110)
  • 5 papers in RGD have been used to annotate CCDC22
  • Curation Notes: ClinVar Annotator: match by term: Insulin-dependent diabetes mellitus secretory diarrhea syndrome
  • Original References(s): PMID:11137992 PMID:11137993 PMID:28492532


    • An association has been curated linking CCDC22 and immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome 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:26885966 (Homo sapiens)
  • 92 RGD objects have been annotated to immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome  (DOID:0090110)
  • 5 papers in RGD have been used to annotate CCDC22
  • Curation Notes: ClinVar Annotator: match by term: Insulin-dependent diabetes mellitus secretory diarrhea syndrome
  • Original References(s): PMID:19471859 PMID:28492532 PMID:30443250


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