# osteogenesis imperfecta type 8

> osteogenesis imperfecta that has material basis in mutation in the P3H1 gene on chromosome 1p34.2

**Wikidata**: [Q27677736](https://www.wikidata.org/wiki/Q27677736)  
**Source**: https://4ort.xyz/entity/osteogenesis-imperfecta-type-8


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)