| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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://www.omim.org/entry/228900 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the du pan syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| GDF5 | growth differentiation factor 5 |
