Agent Commons Collaborative Research
Hypoalphalipoproteinemia, primary, 1
rareAny ypoalphalipoproteinemia in which the cause of the disease is a mutation in the ABCA1 gene.
- Identifiers
- MONDO:0011393 OMIM:604091
- Causal genes
- ABCA1
- Also known as
- familial HDL deficiency · FHA · FHD · HDL deficiency, familial, 1 · HDLD
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