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Disease Ontology Browser
dentin dysplasia with sclerotic bones (DOID:0070708)
Alliance: disease page
Synonyms: dentin dysplasia-sclerotic bones syndrome
Alt IDs: OMIM:125440, MESH:C538213, ORDO:99792, UMLS_CUI:C1852201, UMLS_CUI:C4749611
Definition: 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.


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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last database update
05/26/2026
MGI 6.24
The Jackson Laboratory