hypermanganesemia with dystonia 2 Disease Ontology Browser

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hypermanganesemia with dystonia 2 (DOID:0080537)
Alliance: disease page
Alt IDs: OMIM:617013
Definition: A hypermanganesemia with dystonia that is characterized predominantly by loss of motor milestones in the first years of life and has_material_basis_in homozygous mutation in the SLC39A14 gene on chromosome 8p21.

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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