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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) 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:gastrointestinal system disease
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Accession:DOID:77 term browser browse the term
Definition:A disease of anatomical entity that is located_in the gastrointestinal tract. (DO)
Synonyms:exact_synonym: Cholera Infantum;   Functional Gastrointestinal Disorder;   GIT disease;   Gastrointestinal Diseases;   alimentary system disease;   digestive system disease;   digestive system diseases;   digestive system disorder;   functional gastrointestinal disorders;   gastroenteropathy;   gastrointestinal disease;   gastrointestinal disorder
 primary_id: MESH:D004066;   MESH:D005767
 alt_id: DOID:9005183
 xref: EFO:0000405;   EFO:0010282;   ICD10CM:K92.9;   ICD9CM:520-579.99
 subset: RGD_JBrowse_slim
For additional species annotation, visit the Alliance of Genome Resources.



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  • Term paths to the root
    Path 1
    Term Annotations click to browse term
      disease 18246
        disease of anatomical entity 17610
          gastrointestinal system disease 6656
            Digestive System Abnormalities + 496
            Digestive System Fistula + 51
            Digestive System Neoplasms + 3792
            Gastrointestinal Hemorrhage + 11
            Gastrointestinal Motility Disorders + 78
            Gastrointestinal Neoplasms + 3668
            Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 1
            INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD 1
            Kilquist Syndrome 1
            NATURAL KILLER CELL ENTEROPATHY 13
            Novak Syndrome 0
            Peritoneal Diseases + 78
            Siegler Brewer Carey Syndrome 0
            Visceral Prolapse 0
            appendix disease + 0
            autoimmune disease of gastrointestinal tract + 262
            autosomal recessive cutis laxa type IC 1
            diarrhea + 56
            esophageal disease + 500
            gastroenteritis + 564
            gastrointestinal anthrax + 0
            gastrointestinal tuberculosis + 0
            gastrointestinal tularemia 0
            hepatobiliary disease + 2813
            intestinal disease + 2984
            mouth disease + 874
            pancreas disease + 1174
            stomach disease + 1050
    paths to the root