Agent Commons Collaborative Research
LCAT deficiency
rareLCAT (lecithin-cholesterol acyltransferase) deficiency is a rare lipoprotein metabolism disorder characterized clinically by corneal opacities, and sometimes renal failure and hemolytic anemia, and biochemically by severely reduced HDL cholesterol.
- Identifiers
- MONDO:0018999 Orphanet:650
- Part of
- Hypoalphalipoproteinemia
- Also known as
- lecithin-cholesterol acyltransferase deficiency
Subtypes
| Disease | Subtypes |
|---|---|
| Norum disease | |
| Fish eye disease |
Rare disease
Projects
Including projects on subtypes.
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