cleidocranial dysplasia Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
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1 genes associated with the cleidocranial dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
RUNX2 runt-related transcription factor 2