ocular motor apraxia, Cogan type Disease Ontology Browser

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Disease Ontology Browser

ocular motor apraxia, Cogan type (DOID:0080849)
Alliance: disease page
Alt IDs: OMIM:257550, ORDO:1404
Definition: An eye disease that is characterized by defective or absent horizontal voluntary eye movements, and defective or absent horizontal ocular attraction movements.

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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