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Disease Ontology Browser
osteogenesis imperfecta type 12 (DOID:0110348)
Alliance: disease page
Synonyms: OI12; osteogenesis imperfecta type XII
Alt IDs: OMIM:613849, ICD10CM:Q78.0
Definition: An osteogenesis imperfecta that has_material_basis_in mutation in the SP7 gene on chromosome 12q13.

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)
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Send questions and comments to User Support. 		last database update
11/19/2024
MGI 6.24 		The Jackson Laboratory