mirror movements 1 Disease Ontology Browser

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Disease Ontology Browser

mirror movements 1 (DOID:0070636)
Alliance: disease page
Alt IDs: OMIM:157600
Definition: A congenital mirror movement disorder characterized by mirror movements and/or agenesis of the corpus callosum that has_material_basis_in heterozygous mutation in the DCC gene on chromosome 18q21, with incomplete penetrance.

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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