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