# familial hypobetalipoproteinemia 2

> hypobetalipoproteinemia that has material basis in homozygous or compound heterozygous mutation in the ANGPTL3 gene on chromosome 1p31

**Wikidata**: [Q32146679](https://www.wikidata.org/wiki/Q32146679)  
**Source**: https://4ort.xyz/entity/familial-hypobetalipoproteinemia-2


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)