| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | An osteochondrodysplasia that has_material_basis_in a mutation in chromosome 17 which results_in bowing in the located_in tibia or located_in femur. (Human Disease Ontology, DOID_0050463) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D055036 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Campomelic Dysplasia from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| SOX9 | SRY (sex determining region Y)-box 9 | 2.88009 |
