Hypermanganesemia with dystonia type 1

Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- SLC30A10 / Solute Carrier Family 30 Member 10
  1q41
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Zinc transporter 10
Disease group(s)
- 22.3 Disorders of manganese metabolism