Hypermanganesemia with Dystonia 2 (HMNDYT2)

Hypermanganesemia with Dystonia 2, also known as hmndyt2, is related to hypermanganesemia with dystonia and slc39a14 deficiency. An important gene associated with Hypermanganesemia with Dystonia 2 is SLC39A14 (Solute Carrier Family 39 Member 14), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Nuclear receptors meta-pathway. Affiliated tissues include brain, and related phenotypes are intellectual disability and spasticity