National Cancer Institute Thesaurus

Last uploaded: February 21, 2019

Preferred Name	Hyperlipoproteinemia Type I
ID	http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84771
code	C84771
DEFINITION	A genetic disorder of lipoprotein metabolism caused by mutations in the LPL and apolipoprotein (apo) C-II genes. It is characterized by increased levels of chylomicrons and triglycerides in the blood.
label	Hyperlipoproteinemia Type I
Preferred_Name	Hyperlipoproteinemia Type I
prefixIRI	C84771
prefLabel	Hyperlipoproteinemia Type I
Semantic_Type	Disease or Syndrome
UMLS_CUI	C0023817
subClassOf	http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C34709

Delete	Subject	Author	Type	Created
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Delete	Mapping To	Ontology	Source
	http://purl.bioontology.org/ontology/OMIM/238600	Online Mendelian Inheritance in Man	LOOM
	http://purl.bioontology.org/ontology/MESH/D008072	Medical Subject Headings	LOOM