|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||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. (Human Disease Ontology, DOID_13994)|
|Downloads & Tools|
1 genes associated with the cleidocranial dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
|RUNX2||runt-related transcription factor 2|