OnlineIMD
Iminoglycinuria
Type
Phenotype
External link(s)
Orphanet
IEMbase
VMH
Associated genes
Gene list
SLC6A19
Hartnup disease
SLC36A2
Proton-coupled amino acid transporter 2 deficiency
SLC6A20
Proline imino transporter-asssociated disease
Disease group(s)
1.11 Disorders of amino acid transport