Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Deaf-Blind Disorders
CUI: C1955603
Disease: Deaf-Blind Disorders
0.010 GeneticVariation BEFREE Because the CLRN1(N48K) mutation causes both hearing and vision loss, BF844 could in principle prevent both sensory deficiencies in patients with USH3. 27110679 2016