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Disease Ontology Browser
dentinogenesis imperfecta (DOID:4154)
Alliance: disease page
Alt IDs: OMIM:125490, OMIM:125500, ICD10CM:K00.5, MESH:D003811, NCI:C84667, ORDO:49042, UMLS_CUI:C0011436
Definition: A tooth disease characterized by discolored, opalescent teeth that has_material_basis_in mutation in the DSPP gene on chromosome 4q22.

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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Send questions and comments to User Support. 		last database update
04/09/2024
MGI 6.23 		The Jackson Laboratory