About   Help   FAQ
Disease Ontology Browser
osteogenesis imperfecta type 7 (DOID:0110337)
Alliance: disease page
Synonyms: OI7; osteogenesis imperfecta type VII
Alt IDs: OMIM:610682, ICD10CM:Q78.0, MESH:C565200
Definition: An osteogenesis imperfecta that has_material_basis_in mutation in the CRTAP gene on chromosome 3p22.

Disease References using Mouse Models (2)
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
04/16/2024
MGI 6.23 		The Jackson Laboratory