Gene: BMPR1B ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 658
Gene Symbol: BMPR1B
BMPR1B 		0.300 GeneticVariation disease ORPHANET A novel R486Q mutation in BMPR1B resulting in either a brachydactyly type C/symphalangism-like phenotype or brachydactyly type A2. 16957682 2006