|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An autosomal recessive disease that is characterised by severe reduction or absence of the fibula and complex brachydactyly. (Human Disease Ontology, DOID_0050790)|
|Downloads & Tools|
1 genes/proteins associated with the disease Fibular hypoplasia and complex brachydactyly from the curated CTD Gene-Disease Associations dataset.
|GDF5||growth differentiation factor 5||2.88009|