"MESH:D002973"^^ . "ORDO:1452"^^ . "OMIM:216330"^^ . . _:vb50949344 . _:vb50949344 . "DOID:13994"^^ . . "cleidocranial dysplasia"^^ . "UMLS_CUI:C0008928"^^ . . "GARD:6118"^^ . . _:vb50949344 . "Marie-Sainton Disease"@en . _:vb50949344 . . _:vb50949344 . "ICD10CM:Q74.0"^^ . "SNOMEDCT_US_2021_09_01:65976001"^^ . "cleidocranial dysostosis"@en . "NCI:C75020"^^ . "Xref MGI.\nOMIM mapping confirmed by DO. [SN]."^^ . "An osteochondrodysplasia that has_material_basis_in mutations in the RUNX2 gene which results_in undeveloped or absent located_in clavicle along with delayed closing of fontanels in the located_in skull."^^ . "OMIM:119600"^^ . . "disease_ontology"^^ .