Hypermanganesemia with dystonia 2

MONDO:0014864

Any hypermanganesemia with dystonia in which the cause of the disease is a mutation in the SLC39A14 gene.

Also known as: HMNDYT2, SLC39A14 hypermanganesemia with dystonia, hypermanganesemia with dystonia 2, hypermanganesemia with dystonia 2; HMNDYT2, hypermanganesemia with dystonia caused by mutation in SLC39A14, hypermanganesemia with dystonia type 2

24 clinical trials for this condition and its sub-types.

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