Disease: Albinism, Ocular ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Albinism, Ocular
CUI: C0078917
Disease: Albinism, Ocular
0.010 GeneticVariation BEFREE Here, we present a second WS2 family with OA and provide evidence suggesting the TYR(R402Q) allele does not cause OA in this family. 19938076 2009