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Ontology Browser

Term:
familial chylomicronemia due to inhibition of lipoprotein lipase activity (DOID:0111419)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
cholesterol-ester transfer protein deficiency +   
familial apolipoprotein A5 deficiency  
familial apolipoprotein C-II deficiency  
familial chylomicronemia due to inhibition of lipoprotein lipase activity 
A familial chylomicronemia syndrome characterized by hypertriglyceridemia, chylomicronemia, very low levels of postheparin plasma lipolytic activity, presence in the circulation of a lipoprotein lipase inhibitor, and elevated adipose levels of lipoprotien lipase. (DO)
familial GPIHBP1 deficiency  
familial lipase maturation factor 1 deficiency  
familial lipoprotein lipase deficiency +   
Hyperlipoproteinemia Type II +   
hyperlipoproteinemia type III +   
hyperlipoproteinemia type IV  
hyperlipoproteinemia type V  
Lipoprotein Types--Lp System Lp(A) Hyperlipoproteinemia 

Synonyms
Exact Synonyms: familial chylomicronemia due to circulating inhibitor of lipoprotein lipase ;   hyperlipoproteinemia type 1C ;   hyperlipoproteinemia type IC
Primary IDs: MESH:C566126
Alternate IDs: OMIM:118830
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/6833877 "DO" "DO"

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