About   Help   FAQ
Disease Ontology Browser
osteogenesis imperfecta (DOID:12347)
Alliance: disease page
Synonyms: brittle bone disease; Fragilitas ossium; Lobstein's syndrome; Osteopsathyrosis; Vrolik's disease
Alt IDs: DOID:14708, ICD10CM:Q78.0, ICD9CM:756.51, MESH:D010013, NCI:C26837, OMIM:PS166200, ORDO:666, UMLS_CUI:C0029434
Definition: An osteochondrodysplasia that has_material_basis_in a deficiency in type-I collagen which results_in brittle bones and defective connective tissue.

Disease References using Mouse Models (35)
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
11/05/2024
MGI 6.24 		The Jackson Laboratory