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Disease Ontology Browser
dentin dysplasia type IC (DOID:0070706)
Alliance: disease page
Alt IDs: OMIM:621559
Definition: A dentin dysplasia characterized by tooth crowns that are normal in morphology, form, and color and roots that are short, blunt, and malformed, resulting in severe tooth hypermobility starting in late childhood followed by spontaneous tooth loss around 20 years of age, that has_material_basis_in heterozygous mutation in the SSUH2 gene on chromosome 3p25.

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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05/26/2026
MGI 6.24 		The Jackson Laboratory