National Cancer Institute Thesaurus

Last uploaded: February 21, 2019
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Preferred Name

Gilbert Syndrome
ID

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84729
code

C84729
DEFINITION

An autosomal recessive inherited disorder characterized by unconjugated hyperbilirubinemia, resulting in harmless intermittent jaundice.
FULL_SYN

Gilbert Disease
label

Gilbert Syndrome
Preferred_Name

Gilbert Syndrome
prefixIRI

C84729
prefLabel

Gilbert Syndrome
Semantic_Type

Disease or Syndrome
UMLS_CUI

C0017551
subClassOf

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84761

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C28193
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http://purl.bioontology.org/ontology/ICD10CM/E80.4 International Classification of Diseases, Version 10 - Clinical Modification LOOM
http://purl.obolibrary.org/obo/DOID_2739 Human Disease Ontology 123 LOOM
http://purl.bioontology.org/ontology/OMIM/143500 Online Mendelian Inheritance in Man LOOM