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

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familial chylomicronemia due to inhibition of lipoprotein lipase activity (DOID:0111419)
Alliance: disease page
Alt IDs: OMIM:118830
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.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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