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

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Broader categories

Disease (680) Metabolic disease (233) Nervous system disorder (231) Hereditary disease (176) Inborn errors of metabolism (45) Human disease (14) Hereditary neurological disease (6) Autosomal recessive disease (4) Disease of genetic or genomic mechanism (2) Autosomal genetic disease (0)

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