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 Biomarker group CTD_human A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomalies. 15805157 2005