Gene: GDF5 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8200
Gene Symbol: GDF5
GDF5 		0.020 GeneticVariation disease BEFREE A novel mutation in GDF5 causes autosomal dominant symphalangism in two Chinese families. 16892395 2006
Entrez Id: 8200
Gene Symbol: GDF5
GDF5 		0.020 GeneticVariation disease BEFREE They cause brachydactyly type A2 (L441P) and symphalangism (R438L), conditions previously associated with mutations in the GDF5 receptor bone morphogenetic protein receptor type 1b (BMPR1B) and the BMP antagonist NOGGIN, respectively. 16127465 2005