National Cancer Institute Thesaurus

Last uploaded: February 21, 2019
Preferred Name

Gastroesophageal Reflux Disease

ID

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C26781

ALT_DEFINITION

Reflux of stomach contents with symptoms and/or complications from the reflux act.

A disorder characterized by reflux of the gastric and/or duodenal contents into the distal esophagus. It is chronic in nature and usually caused by incompetence of the lower esophageal sphincter, and may result in injury to the esophageal mucosal. Symptoms include heartburn and acid indigestion.

code

C26781

Concept_In_Subset

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C116977

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C118464

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C90259

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C99147

Contributing_Source

CTRP

NICHD

MedDRA

DEFINITION

A chronic disorder characterized by reflux of the gastric and/or duodenal contents into the distal esophagus. It is usually caused by incompetence of the lower esophageal sphincter. Symptoms include heartburn and acid indigestion. It may cause injury to the esophageal mucosa.

Display_Name

Gastroesophageal Reflux Disease

FULL_SYN

GERD

Has_NICHD_Parent

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C2990

label

Gastroesophageal Reflux Disease

Legacy_Concept_Name

Gastroesophageal_Reflux_Disease

NICHD_Hierarchy_Term

Gastroesophageal Reflux Disease

Preferred_Name

Gastroesophageal Reflux Disease

prefixIRI

C26781

prefLabel

Gastroesophageal Reflux Disease

Semantic_Type

Disease or Syndrome

UMLS_CUI

C0017168

subClassOf

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C53497

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http://purl.bioontology.org/ontology/LNC/LP100601-6 Logical Observation Identifier Names and Codes LOOM
http://purl.bioontology.org/ontology/ICD10CM/K21 International Classification of Diseases, Version 10 - Clinical Modification LOOM
http://purl.obolibrary.org/obo/DOID_8534 Human Disease Ontology 123 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU001906 Online Mendelian Inheritance in Man LOOM