familial chylomicronemia due to inhibition of lipoprotein lipase activity - Ontology Browser

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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

familial chylomicronemia syndrome + is-a

Hyperlipoproteinemias + is-a

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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