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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Hyperlipoproteinemias +     
cholesterol-ester transfer protein deficiency +   
familial chylomicronemia due to inhibition of lipoprotein lipase activity 
familial GPIHBP1 deficiency  
familial lipoprotein lipase deficiency +   
Hyperlipoproteinemia Type II +   
A group of familial disorders characterized by elevated circulating cholesterol contained in either LOW-DENSITY LIPOPROTEINS alone or also in VERY-LOW-DENSITY LIPOPROTEINS (pre-beta lipoproteins).
hyperlipoproteinemia type III +   
hyperlipoproteinemia type IV  
hyperlipoproteinemia type V  
Lipoprotein Types--Lp System Lp(A) Hyperlipoproteinemia 

Synonyms
Exact Synonyms: Autosomal Dominant Hypercholesterolemia ;   Essential Hypercholesterolemia ;   Essential Hypercholesterolemias ;   Familial Combined Hyperlipoproteinemia ;   Familial Combined Hyperlipoproteinemias ;   HYPERCHOLESTEROLEMIA, FAMILIAL, 2 ;   Hyper Low Density Lipoproteinemia ;   Hyper beta Lipoproteinemia ;   Hyper-Low Density Lipoproteinemias ;   Hyper-beta-Lipoproteinemias ;   Hyperbetalipoproteinemia ;   Hyperbetalipoproteinemias ;   Hypercholesterolemia, Autosomal Dominant, Type B ;   Hyperlipoproteinemia Type 2 ;   Hyperlipoproteinemia Type IIa ;   Hyperlipoproteinemia Type IIb ;   LDL Receptor Disorder ;   LDL Receptor Disorders ;   autosomal dominant hypercholesterolemias ;   type II Hyperlipoproteinemias ;   type IIa hyperlipoproteinemias
Broad Synonyms: APOB-RELATED CONDITION ;   APOB-RELATED DISORDER
Primary IDs: MESH:D006938
Alternate IDs: OMIM:144010
Xrefs: NCI:C123416 ;   NCI:C176014
Definition Sources: MESH:D006938

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