About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory