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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
cholesterol-ester transfer protein deficiency +   
familial chylomicronemia due to inhibition of lipoprotein lipase activity 
familial GPIHBP1 deficiency  
familial lipoprotein lipase deficiency +   
Hyperlipoproteinemia Type II +   
hyperlipoproteinemia type III +   
A familial hyperlipidemia that has_material_basis_in by homozygous, compound heterozygous, or heterozygous mutation in the APOE gene on chromosome 19q13. (DO)
hyperlipoproteinemia type IV  
hyperlipoproteinemia type V  
Lipoprotein Types--Lp System Lp(A) Hyperlipoproteinemia 

Synonyms
Exact Synonyms: DYSBETALIPOPROTEINEMIA DUE TO DEFECT IN APOLIPOPROTEIN E-d ;   Dysbetalipoproteinemia ;   FLOATING-BETALIPOPROTEINEMIA ;   Familial Dysbetalipoproteinemia ;   carbohydrate induced hyperlipemia ;   familial hypercholesterolaemia with hyperlipaemia ;   familial hypercholesterolemia with hyperlipemia ;   familial type 3 hyperlipoproteinemia ;   hyperlipoproteinemias type III ;   remnant hyperlipidemia
Narrow Synonyms: HYPERLIPOPROTEINEMIA, TYPE III, ASSOCIATED WITH APOE3(WASHINGTON) ;   hyperlipoproteinemias type III, due to APOE2
Related Synonyms: APOE2 isoforms ;   APOE3(-)-KOCHI ;   APOE3-WASHINGTON ;   APOE5 VARIANT ;   CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO ;   LDLCQ5 ;   apolipoprotein E, deficiency or defect of ;   low density lipoprotein cholesterol level quantitative trait locus 5
Primary IDs: MESH:D006952
Alternate IDs: OMIM:617347
Xrefs: NCI:C34710
Definition Sources: https://omim.org/entry/617347 "DO" "DO"

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