About   Help   FAQ
Disease Ontology Browser
osteogenesis imperfecta type 10 (DOID:0110346)
Alliance: disease page
Synonyms: OI10; osteogenesis imperfecta type X
Alt IDs: OMIM:613848, ICD10CM:Q78.0
Definition: An osteogenesis imperfecta that has_material_basis_in mutation in the SERPINH gene on chromosome 11q13.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
MGI 6.22
The Jackson Laboratory