| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | An osteochondrodysplasia that has_material_basis_in mutation in the FGFR3 gene which affects ossification of cartilage and results_in short limb dwarfism. (Human Disease Ontology, DOID_0080041) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C562937 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Hypochondroplasia from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| FGFR3 | fibroblast growth factor receptor 3 | 2.88009 |
