| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| 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) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D002973 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Cleidocranial Dysplasia from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| RUNX2 | runt-related transcription factor 2 | 2.88009 |
