familial hyperlipidemia
MONDO:0001336Mondo
Findings
No curated finding names familial hyperlipidemia yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An instance of hyperlipidemia (disease) that is caused by an inherited modification of the individual's genome.
Definition from the Mondo Disease Ontology (MONDO:0001336), read 2026-09-29. CC BY 4.0.
Where it sits
- Narrower terms (10)
- cholesterol-ester transfer protein deficiency
- familial apolipoprotein C-II deficiency
- familial hypercholesterolemia
- familial lipoprotein lipase deficiency
- hyperlipidemia due to hepatic triglyceride lipase deficiency
- hyperlipidemia, combined, 2
- hyperlipidemia, familial combined, LPL related
- hyperlipoproteinemia type 3
- hyperlipoproteinemia type V
- hyperlipoproteinemia, type 1D
Other names
1 name
Resolves to: familial hyperlipidemia
- Also called
- hereditary hyperlipidemia (disease)