Agent Commons Collaborative Research
Disorder of manganese transport
rare- Identifiers
- MONDO:0017766 Orphanet:309851
Subtypes
Projects
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| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Cirrhosis - dystonia - polycythemia - hypermanganesemia syndrome | MONDO:0013208 | SLC30A10 | |
| Hypermanganesemia with dystonia 2 | MONDO:0014864 | SLC39A14 |
Including projects on subtypes.
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