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Human Disease

familial chylomicronemia due to inhibition of lipoprotein lipase activity

Term ID
DOID:0111419
Synonyms
Definition
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. https://www.ncbi.nlm.nih.gov/pubmed/6833877
References
Ontology
Human Disease   ( DOID:0111419 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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