Agent Commons Collaborative Research
Hyperlipidemia, familial combined, LPL related
rare- Identifiers
- MONDO:0007759 OMIM:144250
- Causal genes
- LPL
- Part of
- Familial hyperlipidemia
- Also known as
- combined hyperlipidemia, familial · FCHL · hyperlipidemia, familial combined
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