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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 +   
Pathological processes in the ESOPHAGUS.
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 +   
mouth disease +   
NATURAL KILLER CELL ENTEROPATHY  
Novak Syndrome 
pancreas disease +   
Peritoneal Diseases +   
Phospholipase A2, Group IVA, Deficiency of  
Siegler Brewer Carey Syndrome 
stomach disease +   
Visceral Prolapse 

Synonyms
Exact Synonyms: esophageal diseases
Narrow Synonyms: esophageal ulcer
Primary IDs: MESH:D004935
Alternate IDs: RDO:0004977
Xrefs: ICD10CM:K22.9 ;   ICD9CM:530 ;   ICD9CM:530.9 ;   NCI:C3027
Definition Sources: MESH:D004935, http://en.wikipedia.org/wiki/Esophageal_disease

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