DO_rare_slim has material basis in autosomal dominant disease dentin dysplasia type II ORDO:99791 UMLS_CUI:C0399380 DD-II MESH:D003784 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. MIM:125420 disease_ontology UMLS_CUI:C0399380 MIM:125420 DOID:0070707 ORDO:99791 GARD:1806 SNOMEDCT_US_2025_09_01:109494000 GARD:1806 coronal dentin dysplasia dentin dysplasia autosomal dominant inheritance