OnlineIMD
Cystinuria type A
Type
Disease
External link(s)
Orphanet
IEMbase
VMH
Gene
SLC3A1
/ Solute Carrier Family 3 Member 1
2p21
OMIM
GnomAD
Ensembl
HGNC
VMH
LOVD
Gene product
4F2hc (4F2 cell-surface antigen heavy chain)
Parent entry
Cystinuria
Child entries
Hypotonia-cystinuria syndrome
Hypotonia-cystinuria syndrome, atypical