SLC7A7, solute carrier family 7 member 7, 9056

N. diseases: 122; N. variants: 53
Disease: Amino Acid Metabolism, Inborn Errors ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		0.300 Biomarker group CTD_human Vascular endothelial dysfunction resulting from L-arginine deficiency in a patient with lysinuric protein intolerance. 11544277 2001