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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)
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12/10/2024
MGI 6.24 		The Jackson Laboratory