OnlineIMD
Hartnup disease
Type
Disease
External link(s)
Orphanet
IEMbase
VMH
Gene
SLC6A19
/ Solute Carrier Family 6 Member 19
5p15.33
OMIM
GnomAD
Ensembl
HGNC
VMH
LOVD
Gene product
Neutral amino acid transporter B(0)
Disease group(s)
1.11 Disorders of amino acid transport