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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H01938 | Hypermanganesemia with dystonia | ... (HMNDYT) is an autosomal recessive disorder of manganese (Mn) homeostasis. Loss-of-function mutations in SLC30A10, a Mn efflux transporter, or SLC39A14, a Mn influx transporter, increase Mn levels in blood ... | Hematologic disease |
(HMNDYT1) SLC30A10 [HSA:55532] [KO:K14697] (HMNDYT2) SLC39A14 [HSA:23516] [KO:K14720] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |