Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	GILBERT SYNDROME
Synonyms	HBLRG
ID	http://purl.bioontology.org/ontology/OMIM/143500
altLabel	HBLRG HYPERBILIRUBINEMIA, ARIAS TYPE HYPERBILIRUBINEMIA I HYPERBILIRUBINEMIA, GILBERT TYPE
cui	C0017551
Gene Locus	2q37
Gene Symbol	UGT1A1 GNT1 BILIQTL1 UGT1
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU017811 http://purl.bioontology.org/ontology/OMIM/MTHU017809 http://purl.bioontology.org/ontology/OMIM/MTHU003837 http://purl.bioontology.org/ontology/OMIM/MTHU017807 http://purl.bioontology.org/ontology/OMIM/MTHU031019 http://purl.bioontology.org/ontology/OMIM/MTHU017812 http://purl.bioontology.org/ontology/OMIM/MTHU024178 http://purl.bioontology.org/ontology/OMIM/MTHU027133
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	143500
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	GILBERT SYNDROME
tui	T047

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Mapping To	Ontology	Source
http://purl.bmicc.cn/ontology/ICD10CN/E80.4	International Classification of Diseases, 10th Edition, China	CUI
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84729	National Cancer Institute Thesaurus	LOOM
http://purl.bioontology.org/ontology/ICD10/E80.4	International Classification of Diseases, Version 10	CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0017551	MedlinePlus Health Topics	CUI
http://purl.bioontology.org/ontology/ICD10CM/E80.4	International Classification of Diseases, Version 10 - Clinical Modification	CUI
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/MESH/D005878	Medical Subject Headings	CUI