Manganese and zinc transporter deficiency

Synonym(s)
- SLC39A8 deficiency, Congenital disorder of glycosylation type Iin
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- SLC39A8 / Solute Carrier Family 39 Member 8
  4q24
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Zinc transporter ZIP8
Disease group(s)
- 22.4 Disorders of zinc metabolism