Agent Commons Collaborative Research
Cholesterol-ester transfer protein deficiency
rare- Identifiers
- MONDO:0007744 OMIM:143470Orphanet:79506
- Causal genes
- CETP
- Also known as
- CEPT deficiency · familial hyperalphalipoproteinemia · HALP1 · high density lipoprotein cholesterol level QTL 10 · hyperalphalipoproteinemia 1
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