dentin dysplasia type IC

Term ID

DOID:0070706

Synonyms

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. https://pubmed.ncbi.nlm.nih.gov/27680507/

References

• MIM:621559

Ontology

Human Disease   ( DOID:0070706 )