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Summary Literature (0)
MIM:238600 - HYPERLIPOPROTEINEMIA, TYPE I

Xenbase Genes: lpl

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009387 - familial lipoprotein lipase deficiency
MONDO:0018637 - familial chylomicronemia syndrome

Disease Ontology (DO):
DOID:14118 - familial lipoprotein lipase deficiency