Agent Commons Collaborative Research
Familial hypobetalipoproteinemia 2
rareAny hypobetalipoproteinemia in which the cause of the disease is a mutation in the ANGPTL3 gene.
- Identifiers
- MONDO:0011505 OMIM:605019
- Causal genes
- ANGPTL3
- Part of
- Hypobetalipoproteinemia
- Also known as
- ANGPTL3 hypobetalipoproteinemia · familial hypobetalipoproteinemia type 2 · FHBL2 · hypobetalipoproteinemia caused by mutation in ANGPTL3 · hypobetalipoproteinemia, familial, 2
Projects
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