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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
autoimmune disorder of gastrointestinal tract +   
benign digestive system neoplasm +   
caudal duplication 
chemotherapy-induced gastrointestinal mucositis 
Chilaiditi Syndrome 
colon diverticulum 
common mesentery 
congenital enteropathy due to enteropeptidase deficiency 
Cronkhite-Canada syndrome 
diarrheal disease +   
digestive duplication 
Digestive System Adenoma +   
digestive system cancer +   
digestive system infectious disorder +   
digestive system neuroendocrine neoplasm +   
disease of peritoneum +   
diverticulosis of bowel, hernia, and retinal detachment 
dysplastic oral keratinocyte 
enterocolitis +   
epiglottitis +  
esophageal disease +   
flatulence 
gastric outlet obstruction 
gastroesophageal disease 
gastrointestinal disease +   
gastrointestinal polyp +  
gastrointestinal ulceration, recurrent, with dysfunctional platelets 
Genetic digestive tract tumor +  
growth retardation-mild developmental delay-chronic hepatitis syndrome 
hepatobiliary disease +   
hereditary mixed polyposis syndrome 
hyperplastic polyposis syndrome +  
intestinal disease +   
juvenile polyposis syndrome +  
lingual thyroid 
Meckel's diverticulum 
mouth disease +   
A disease involving the mouth. Any disease of the oral cavity
Moyamoya disease with early-onset achalasia 
nasopharyngitis +  
neoplasm of oropharynx +   
pancreas disease +   
peptic ulcer disease +   
peritonitis +   
small intestine enteropathy  
splenic infarction 
stomach disease +   
stomach diverticulum 
thoraco-abdominal enteric duplication 
tonsillitis +   
umbilical cord ulceration-intestinal atresia syndrome 

Synonyms
Exact Synonyms: DOID:403 ;   NCIT:C3240 ;   disease of mouth ;   disease of the mouth ;   disease or disorder of mouth ;   disorder of mouth ;   http://identifiers.org/medgen/6448 ;   http://identifiers.org/mesh/D009059 ;   http://identifiers.org/snomedct/118938008 ;   http://linkedlifedata.com/resource/umls/id/C0026636
Xrefs: DOID:403 ;   ICD10:K13 ;   ICD10:K14 ;   ICD9:528.9 ;   MEDGEN:6448 ;   MESH:D009059 ;   MONDO:0006858 ;   NCI:C3240 ;   SCTID:118938008 ;   SNOMEDCT:118938008
External Ontologys: disease_has_location EFO:UBERON:0000165 ;   in_taxon EFO:NCBITaxon:9606
Definition Sources: https://orcid.org/0000-0002-6601-2165

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