Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 200894
Gene Symbol: ARL13B
ARL13B
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases 		0.010 GeneticVariation BEFREE Thus our data identify a novel ARL13B variant that causes JS and retinopathy and suggest an extension of the phenotypic spectrum of ARL13B mutations to obesity. 25138100

2015