Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking MYH9 and hemorrhagic disease 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:8564039 (Homo sapiens)
  • 2469 RGD objects have been annotated to hemorrhagic disease  (DOID:2213)
  • 34 papers in RGD have been used to annotate MYH9
  • Curation Notes: ClinVar Annotator: match by term: Abnormal bleeding
  • Original References(s): PMID:10973259 PMID:11776386 PMID:12533692 PMID:15339844 PMID:16098078 PMID:16162639 PMID:17655694 PMID:18059020 PMID:20301740 PMID:21542825 PMID:22627578 PMID:24186861 PMID:25741868 PMID:26056797 PMID:28492532 PMID:30916803 PMID:32100410 PMID:32545517 PMID:34310475


  • An association has been curated linking MYH9 and hemorrhagic disease 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:8564037 (Homo sapiens)
  • 2469 RGD objects have been annotated to hemorrhagic disease  (DOID:2213)
  • 34 papers in RGD have been used to annotate MYH9
  • Curation Notes: ClinVar Annotator: match by term: Abnormal bleeding
  • Original References(s): PMID:10739770 PMID:10973259 PMID:10973260 PMID:11159552 PMID:11590545 PMID:15339844 PMID:19572073 PMID:20301740 PMID:21833445 PMID:23207509 PMID:24186861 PMID:25741868 PMID:28492532 PMID:29068549 PMID:29090586 PMID:32545517 PMID:33855781 PMID:36404341


  • Go Back to source page   Continue to Ontology report