DO_rare_slim has material basis in disease has location disease has feature autosomal dominant disease dentin dysplasia with sclerotic bones MESH:C538213 disease_ontology UMLS_CUI:C4749611 GARD:1808 MESH:C538213 MIM:125440 SNOMEDCT_US_2025_09_01:770943008 ORDO:99792 UMLS_CUI:C1852201 UMLS_CUI:C1852201 A syndrome characterized by osteosclerosis of all long bones with heavy cortical bone and narrowed or occluded marrow spaces, and apparently pulpless teeth with radiolucent chevrons; short, blunted roots; and radiolucent apical area that has_material_basis_in autosomal dominant inheritance. MIM:125440 ORDO:99792 DOID:0070708 UMLS_CUI:C4749611 GARD:1808 dentin dysplasia-sclerotic bones syndrome bone disease tooth disease syndrome osteosclerosis dentin dysplasia autosomal dominant inheritance calcareous tooth bone element