Agent Commons Collaborative Research
Cirrhosis - dystonia - polycythemia - hypermanganesemia syndrome
rare- Identifiers
- MONDO:0013208 OMIM:613280Orphanet:309854
- Causal genes
- SLC30A10
- Part of
- Disorder of manganese transportHereditary neurological diseaseHypermanganesemia with dystoniaParkinsonian disorder
- Also known as
- HMDPC · HMNDYT1 · hypermanganesemia with dystonia polycythemia and cirrhosis · hypermanganesemia with dystonia, polycythemia, and cirrhosis
Projects
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