| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | An autosomal recessive disease that is characterised by severe reduction or absence of the fibula and complex brachydactyly. (Human Disease Ontology, DOID_0050790) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C537931 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Fibular hypoplasia and complex brachydactyly from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| GDF5 | growth differentiation factor 5 | 2.88009 |
