SLC4A4, solute carrier family 4 member 4, 8671

N. diseases: 14; N. variants: 10
Disease: Corneal Opacity ×
Source: CURATED ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity 		0.300 Biomarker phenotype CTD_human G418-mediated ribosomal read-through of a nonsense mutation causing autosomal recessive proximal renal tubular acidosis. 18614622 2008