hypermanganesemia with dystonia 1 Disease Ontology Browser

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hypermanganesemia with dystonia 1 (DOID:0080536)
Alliance: disease page
Alt IDs: OMIM:613280
Definition: A hypermanganesemia with dystonia that is characterized by increased serum manganese, motor neurodegeneration with extrapyramidal features, polycythemia, and hepatic dysfunction and has_material_basis_in homozygous mutation in the SLC30A10 gene on chromosome 1q41.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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