Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 25861
Gene Symbol: WHRN
WHRN
CUI: C1568249
Disease: Usher Syndrome, Type II
Usher Syndrome, Type II
0.940 Biomarker MGD Mice carrying a targeted disruption near the N-terminus of whirlin manifest retinal and inner ear defects, reproducing the clinical features of human USH2 disease. 20502675

2010