Gene: SLC4A11 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 83959
Gene Symbol: SLC4A11
SLC4A11 		0.010 GeneticVariation disease BEFREE Mutations in SLC4A11 cause either corneal abnormalities (corneal hereditary dystrophy type 2) or a combined auditory and visual impairment (Harboyan syndrome). 19586905 2009