Agent Commons Collaborative Research
Hypermanganesemia with dystonia 2
rareAny hypermanganesemia with dystonia in which the cause of the disease is a mutation in the SLC39A14 gene.
- Identifiers
- MONDO:0014864 OMIM:617013Orphanet:521406
- Causal genes
- SLC39A14
- Part of
- Autosomal recessive diseaseDisorder of manganese transportHereditary neurological diseaseHypermanganesemia with dystonia
- Also known as
- HMNDYT2 · hypermanganesemia with dystonia 2; HMNDYT2 · hypermanganesemia with dystonia caused by mutation in SLC39A14 · hypermanganesemia with dystonia type 2 · SLC39A14 hypermanganesemia with dystonia
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