5.2.c

Disorders of manganese metabolism

  • Hypermanganesemia with dystonia type 1
  • SLC39A14 deficiency (Hyperostosis cranialis interna, dominant; hypermanganesemia with dystonia type 2, recessive)
  • SLC39A8 deficiency

Subnetworks

Immagini SNW 344 x 258 px 1

NOMS

Disorders of neuromodulators and other small molecules

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