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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, NCI:C99003, OMIM:PS166200, ORDO:666, UMLS_CUI:C0023931, 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 (33)

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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last database update
02/18/2020
MGI 6.14
The Jackson Laboratory