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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 21140
        disease of anatomical entity 18187
          gastrointestinal system disease 7003
            Digestive System Abnormalities + 510
            Digestive System Fistula + 52
            Digestive System Neoplasms + 3842
            Gastrointestinal Hemorrhage + 12
            Gastrointestinal Motility Disorders + 78
            Gastrointestinal Neoplasms + 3717
            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 + 81
            Siegler Brewer Carey Syndrome 0
            Visceral Prolapse 0
            appendix disease + 0
            autoimmune disease of gastrointestinal tract + 270
            autosomal recessive cutis laxa type IC 1
            diarrhea + 108
            esophageal disease + 502
            gastroenteritis + 565
            gastrointestinal anthrax + 0
            gastrointestinal toxicity 0
            gastrointestinal tuberculosis + 0
            gastrointestinal tularemia 0
            hepatobiliary disease + 3035
            intestinal disease + 3071
            mouth disease + 975
            pancreas disease + 1211
            stomach disease + 1073
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