familial chylomicronemia syndrome

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Summary

Literature (0)

DOID:0111417 - familial chylomicronemia syndrome

Disease Ontology Definition:A familial hyperlipidemia characterized by hypertriglyceridemia and fasting chylomicronemia.

Synonyms:

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: apoa5, lpl, lmf1, apoc2

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): familial hyperlipidemia (is_a)