# osteogenesis imperfecta type 10

> osteogenesis imperfecta that has material basis in mutation in the SERPINH gene on chromosome 11q13

**Wikidata**: [Q27677744](https://www.wikidata.org/wiki/Q27677744)  
**Source**: https://4ort.xyz/entity/osteogenesis-imperfecta-type-10


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Homozygosity for a missense mutation in SERPINH1, which encodes the collagen chaperone protein HSP47, results in severe recessive osteogenesis imperfecta
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)