About   Help   FAQ
Disease Ontology Browser
dentin dysplasia type II (DOID:0070707)
Alliance: disease page
Synonyms: coronal dentin dysplasia; DD-II
Alt IDs: OMIM:125420, ORDO:99791, UMLS_CUI:C0399380
Definition: A dentin dysplasia characterized by primary teeth with discoloration and obliteration of the pulp chamber, and secondary teeth with normal coloration, pulps shaped like thistles or tubes, and ovoid pulp stones that has_material_basis_in heterozygous mutation in the DSPP gene on chromosome 4q22.

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
05/26/2026
MGI 6.24 		The Jackson Laboratory