| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | An osteochondrodysplasia that results_in dwarfism which has_material_basis_in abnormal ossification of cartilage in located_in long bone. (Human Disease Ontology, DOID_4480) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D000130 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Achondroplasia from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| FGFR3 | fibroblast growth factor receptor 3 | 2.88009 |
