Source: CLINGEN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55814
Gene Symbol: BDP1
BDP1
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.300 Biomarker CLINGEN Linkage study and exome sequencing identify a BDP1 mutation associated with hereditary hearing loss. 24312468

2013