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Disease Ontology Browser
dentin dysplasia type IA (DOID:0070704)
Alliance: disease page
Synonyms: atypical dentin dysplasia due to SMOC2 deficiency
Alt IDs: OMIM:125400, ORDO:314721, UMLS_CUI:C5190802
Definition: A dentin dysplasia characterized by oligodontia, microdontia with very globular and malformed teeth and incisal notches, taurodontism of the molar teeth, and short roots that has_material_basis_in homozygous mutation in the SMOC2 gene on chromosome 6q27.

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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
05/26/2026
MGI 6.24 		The Jackson Laboratory