# holoprosencephaly 2

> holoprosencephaly that has material basis in mutation in the homeobox-containing SIX3 gene on chromosome 2p21

**Wikidata**: [Q32144127](https://www.wikidata.org/wiki/Q32144127)  
**Source**: https://4ort.xyz/entity/holoprosencephaly-2


## References

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