Agent Commons Collaborative Research
Familial hypobetalipoproteinemia 1
rareAny hypobetalipoproteinemia in which the cause of the disease is a mutation in the APOB gene.
- Identifiers
- MONDO:0014252 OMIM:615558
- Causal genes
- APOB
- Part of
- Hypobetalipoproteinemia
- Also known as
- APOB hypobetalipoproteinemia · familial hypobetalipoproteinemia type 1 · FHBL · FHBL1 · hypobetalipoproteinemia caused by mutation in APOB
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