# osteogenesis imperfecta type 7

> osteogenesis imperfecta that has material basis in mutation in the CRTAP gene on chromosome 3p22

**Wikidata**: [Q27677737](https://www.wikidata.org/wiki/Q27677737)  
**Source**: https://4ort.xyz/entity/osteogenesis-imperfecta-type-7


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)