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GENE - TERM ANNOTATION REPORT

16 Annotations Found.

An association has been curated linking MYCN and Feingold syndrome in Homo sapiens.        

  • The association was inferred from experiment (EXP)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 3 RGD objects have been annotated to Feingold syndrome  (DOID:0060464)
  • 5 papers in RGD have been used to annotate MYCN
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:19852433 PMID:21532573


    • An association has been curated linking MYCN and Feingold 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:8599594 (Homo sapiens)
  • 3 RGD objects have been annotated to Feingold syndrome  (DOID:0060464)
  • 5 papers in RGD have been used to annotate MYCN
  • Curation Notes: ClinVar Annotator: match by term: Digital anomalies with short palpebral fissures and atresia of esophagus, or duodenum
  • Original References(s): PMID:15821734


    • An association has been curated linking MYCN and Feingold 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:13211770 (Homo sapiens)
  • 3 RGD objects have been annotated to Feingold syndrome  (DOID:0060464)
  • 5 papers in RGD have been used to annotate MYCN
  • Curation Notes: ClinVar Annotator: match by term: Digital anomalies with short palpebral fissures and atresia of esophagus, or duodenum
  • Original References(s): PMID:15821734 PMID:18470948 PMID:20301770 PMID:25741868


    • An association has been curated linking MYCN and Feingold 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:8599596 (Homo sapiens)
  • 3 RGD objects have been annotated to Feingold syndrome  (DOID:0060464)
  • 5 papers in RGD have been used to annotate MYCN
  • Curation Notes: ClinVar Annotator: match by term: Digital anomalies with short palpebral fissures and atresia of esophagus, or duodenum
  • Original References(s): PMID:18470948


    • An association has been curated linking MYCN and Feingold 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:8599595 (Homo sapiens)
  • 3 RGD objects have been annotated to Feingold syndrome  (DOID:0060464)
  • 5 papers in RGD have been used to annotate MYCN
  • Curation Notes: ClinVar Annotator: match by term: Digital anomalies with short palpebral fissures and atresia of esophagus, or duodenum
  • Original References(s): PMID:15821734 PMID:18470948 PMID:20301770


    • An association has been curated linking MYCN and Feingold 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:8599597 (Homo sapiens)
  • 3 RGD objects have been annotated to Feingold syndrome  (DOID:0060464)
  • 5 papers in RGD have been used to annotate MYCN
  • Curation Notes: ClinVar Annotator: match by term: Digital anomalies with short palpebral fissures and atresia of esophagus, or duodenum
  • Original References(s): PMID:16906565 PMID:18470948


    • An association has been curated linking MYCN and Feingold 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:8599593 (Homo sapiens)
  • 3 RGD objects have been annotated to Feingold syndrome  (DOID:0060464)
  • 5 papers in RGD have been used to annotate MYCN
  • Curation Notes: ClinVar Annotator: match by term: MMT syndrome
  • Original References(s): PMID:15821734 PMID:18470948 PMID:20301770 PMID:30655312


    • An association has been curated linking MYCN and Feingold 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:155798501 (Homo sapiens)
  • 3 RGD objects have been annotated to Feingold syndrome  (DOID:0060464)
  • 5 papers in RGD have been used to annotate MYCN
  • Curation Notes: ClinVar Annotator: match by term: MICROCEPHALY AND DIGITAL ABNORMALITIES WITH NORMAL INTELLIGENCE
  • Original References(s): PMID:25741868 PMID:30573562


    • An association has been curated linking MYCN and Feingold 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:25318685 (Homo sapiens)
  • 3 RGD objects have been annotated to Feingold syndrome  (DOID:0060464)
  • 5 papers in RGD have been used to annotate MYCN
  • Curation Notes: ClinVar Annotator: match by term: MICROCEPHALY AND DIGITAL ABNORMALITIES WITH NORMAL INTELLIGENCE
  • Original References(s): PMID:18470948 PMID:21224895 PMID:25741868 PMID:28492532 PMID:30573562


    • An association has been curated linking MYCN and Feingold 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:156009922 (Homo sapiens)
  • 3 RGD objects have been annotated to Feingold syndrome  (DOID:0060464)
  • 5 papers in RGD have been used to annotate MYCN
  • Curation Notes: ClinVar Annotator: match by term: MICROCEPHALY AND DIGITAL ABNORMALITIES WITH NORMAL INTELLIGENCE
  • Original References(s): PMID:15821734 PMID:25741868 PMID:28492532


    • An association has been curated linking MYCN and Feingold 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:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens) & RGD:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens) & RGD:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens) & RGD:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens) & RGD:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens) & RGD:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens) & RGD:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens) & RGD:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens) & RGD:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens) & RGD:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens) & RGD:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens) & RGD:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens) & RGD:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens) & RGD:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens) & RGD:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens) & RGD:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens) & RGD:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens) & RGD:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens) & RGD:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens) & RGD:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens) & RGD:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens) & RGD:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens) & RGD:13211387|RGD:13212170|RGD:13212262|RGD:150453198|RGD:150455643|RGD:150546111|RGD:152977819|RGD:152980916|RGD:155268037|RGD:155642982|RGD:155643394|RGD:155644946|RGD:243049261|RGD:329355714|RGD:329848871|RGD:329952662|RGD:38596766|RGD:401723739|RGD:401731694|RGD:401860644|RGD:401868998|RGD:404977484|RGD:405257264 (Homo sapiens)
  • 3 RGD objects have been annotated to Feingold syndrome  (DOID:0060464)
  • 5 papers in RGD have been used to annotate MYCN
  • Curation Notes: ClinVar Annotator: match by term: Digital anomalies with short palpebral fissures and atresia of esophagus, or duodenum | ClinVar Annotator: match by term: MICROCEPHALY AND DIGITAL ABNORMALITIES WITH NORMAL INTELLIGENCE | ClinVar Annotator: match by term: Microcephaly-oculo-digito-esophageal-duodenal syndrome
  • Original References(s): PMID:25741868


    • An association has been curated linking MYCN and Feingold 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:151661193|RGD:39456677 (Homo sapiens) & RGD:151661193|RGD:39456677 (Homo sapiens)
  • 3 RGD objects have been annotated to Feingold syndrome  (DOID:0060464)
  • 5 papers in RGD have been used to annotate MYCN
  • Curation Notes: ClinVar Annotator: match by term: MICROCEPHALY AND DIGITAL ABNORMALITIES WITH NORMAL INTELLIGENCE


    • An association has been curated linking MYCN and Feingold 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:13531617|RGD:13540164|RGD:13541815|RGD:15104101|RGD:15106992|RGD:15113085|RGD:152091477 (Homo sapiens) & RGD:13531617|RGD:13540164|RGD:13541815|RGD:15104101|RGD:15106992|RGD:15113085|RGD:152091477 (Homo sapiens) & RGD:13531617|RGD:13540164|RGD:13541815|RGD:15104101|RGD:15106992|RGD:15113085|RGD:152091477 (Homo sapiens) & RGD:13531617|RGD:13540164|RGD:13541815|RGD:15104101|RGD:15106992|RGD:15113085|RGD:152091477 (Homo sapiens) & RGD:13531617|RGD:13540164|RGD:13541815|RGD:15104101|RGD:15106992|RGD:15113085|RGD:152091477 (Homo sapiens) & RGD:13531617|RGD:13540164|RGD:13541815|RGD:15104101|RGD:15106992|RGD:15113085|RGD:152091477 (Homo sapiens) & RGD:13531617|RGD:13540164|RGD:13541815|RGD:15104101|RGD:15106992|RGD:15113085|RGD:152091477 (Homo sapiens)
  • 3 RGD objects have been annotated to Feingold syndrome  (DOID:0060464)
  • 5 papers in RGD have been used to annotate MYCN
  • Curation Notes: ClinVar Annotator: match by term: MICROCEPHALY AND DIGITAL ABNORMALITIES WITH NORMAL INTELLIGENCE
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking MYCN and Feingold 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:8563954|RGD:8599598 (Homo sapiens) & RGD:8563954|RGD:8599598 (Homo sapiens)
  • 3 RGD objects have been annotated to Feingold syndrome  (DOID:0060464)
  • 5 papers in RGD have been used to annotate MYCN
  • Curation Notes: ClinVar Annotator: match by term: Digital anomalies with short palpebral fissures and atresia of esophagus, or duodenum
  • Original References(s): PMID:18671284


    • An association has been curated linking MYCN and Feingold 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:13211466 (Homo sapiens)
  • 3 RGD objects have been annotated to Feingold syndrome  (DOID:0060464)
  • 5 papers in RGD have been used to annotate MYCN
  • Curation Notes: ClinVar Annotator: match by term: Digital anomalies with short palpebral fissures and atresia of esophagus, or duodenum
  • Original References(s): PMID:15821734 PMID:25741868 PMID:28492532 PMID:33442900


    • An association has been curated linking MYCN and Feingold 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:13705268|RGD:15098328 (Homo sapiens) & RGD:13705268|RGD:15098328 (Homo sapiens)
  • 3 RGD objects have been annotated to Feingold syndrome  (DOID:0060464)
  • 5 papers in RGD have been used to annotate MYCN
  • Curation Notes: ClinVar Annotator: match by term: Digital anomalies with short palpebral fissures and atresia of esophagus, or duodenum
  • Original References(s): PMID:18470948 PMID:20301770


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