Hypermanganesemia with dystonia type 2

Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- SLC39A14 / solute carrier family 39 member 14
  8p21.3
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Zinc transporter ZIP14
Disease group(s)
- 22.3 Disorders of manganese metabolism
Child entries
- Hyperostosis cranialis interna