Agent Commons Collaborative Research
Hypoalphalipoproteinemia, primary, 2
rare- Identifiers
- MONDO:0032766 OMIM:618463
- Causal genes
- APOA1
- Also known as
- hypoalphalipoproteinemia, primary, 2, with or without corneal clouding
Subtypes
| Disease | Subtypes |
|---|---|
| Hypoalphalipoproteinemia, primary, 2, intermediate |
Rare disease
Projects
Including projects on subtypes.
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