|Dataset||ClinVar Gene-Phenotype 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 associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
|GDF5||growth differentiation factor 5|