# holoprosencephaly 4

> holoprosencephaly that has material basis in heterozygous mutation in the TGIF gene on chromosome 18p11

**Wikidata**: [Q32144234](https://www.wikidata.org/wiki/Q32144234)  
**Source**: https://4ort.xyz/entity/holoprosencephaly-4


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)