Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
appendix disease +  
autosomal recessive cutis laxa type IC  
biliary tract disease +   
diarrhea +   
Digestive System Abnormalities +   
Digestive System Fistula +   
Digestive System Neoplasms +   
esophageal disease +   
gastroenteritis +   
gastrointestinal anthrax +  
Gastrointestinal Diseases +   
Gastrointestinal Hemorrhage +   
Gastrointestinal Motility Disorders +   
Gastrointestinal Neoplasms +   
gastrointestinal tuberculosis +  
gastrointestinal tularemia 
hepatobiliary disease +   
INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD  
intestinal disease +   
Pathological processes in any segment of the INTESTINE from DUODENUM to RECTUM.
mouth disease +   
Novak Syndrome 
pancreas disease +   
Peritoneal Diseases +   
Phospholipase A2, Group IVA, Deficiency of 
Siegler Brewer Carey Syndrome 
stomach disease +   
Visceral Prolapse 
 cecal disease +   
 colonic disease +   
 diverticulitis +   
 dysentery +  
 Enteritis +   
 Enterocolitis +   
 Ileal Diseases +   
 inguinal hernia +   
 rectal disease +   
 steatorrhea +   

Synonyms
Exact Synonyms: intestinal diseases
Narrow Synonyms: Lundehund syndrome
Primary IDs: MESH:D007410 ;   RDO:0000119
Alternate IDs: OMIA:002031
Definition Sources: MESH:D007410, http://en.wikipedia.org/wiki/Human_gastrointestinal_tract

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.