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RGD uses the Human Disease Ontology (DO, for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:Diarrhea prodrome + Hemolytic-Uremic Syndrome
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Accession:DOID:9003168 term browser browse the term
Synonyms:exact_synonym: Diarrhea prodrome + HUS
 primary_id: MESH:C531700;   RDO:0000123
For additional species annotation, visit the Alliance of Genome Resources.

show annotations for term's descendants           Sort by:
Diarrhea prodrome + Hemolytic-Uremic Syndrome term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Gp1ba glycoprotein Ib platelet subunit alpha ISO associated with Escherichia Coli Infections;DNA:SNP:exon: (rs121908064) (human) RGD PMID:29216383 RGD:42722620 NCBI chr10:55,352,938...55,355,804
Ensembl chr10:55,352,899...55,356,774
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17941
    syndrome 9341
      Diarrhea prodrome + Hemolytic-Uremic Syndrome 1
Path 2
Term Annotations click to browse term
  disease 17941
    disease of anatomical entity 17296
      Hemic and Lymphatic Diseases 3150
        hematopoietic system disease 2697
          blood coagulation disease 832
            hemorrhagic disease 801
              blood platelet disease 316
                thrombocytopenia 240
                  Thrombotic Microangiopathies 76
                    hemolytic-uremic syndrome 35
                      Diarrhea prodrome + Hemolytic-Uremic Syndrome 1
paths to the root