Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8419
Gene Symbol: BFSP2
BFSP2
CUI: C0086543
Disease: Cataract
Cataract
0.390 GeneticVariation LHGDN The progressive phenotype has provided more evidence for the heterogeneity of congenital cataract caused by BFSP2 mutations and for the important role BFSP2 plays in cataract formation. 17982427

2007