Search Ontology:

Human Disease

familial chylomicronemia syndrome

Term ID

DOID:0111417

Synonyms

Definition

A familial hyperlipidemia characterized by hypertriglyceridemia and fasting chylomicronemia. https://www.ncbi.nlm.nih.gov/pubmed/23525082

References

ORDO:444490

Ontology

Human Disease ( DOID:0111417 )

Relationships

is a type of: familial hyperlipidemia

familial hyperlipidemia Show first 5 Terms
has subtype: familial apolipoprotein A5 deficiency familial apolipoprotein C-II deficiency familial chylomicronemia due to inhibition of lipoprotein lipase activity familial GPIHBP1 deficiency familial lipase maturation factor 1 deficiency ... Show All 6 Terms

familial apolipoprotein A5 deficiency familial apolipoprotein C-II deficiency familial chylomicronemia due to inhibition of lipoprotein lipase activity familial GPIHBP1 deficiency familial lipase maturation factor 1 deficiency familial lipoprotein lipase deficiency Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models