infantile cerebellar-retinal degeneration Disease Ontology Browser

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Disease Ontology Browser

infantile cerebellar-retinal degeneration (DOID:0050883)
Alliance: disease page
Alt IDs: OMIM:614559
Definition: A neurodegenerative disease that is characterized by onset between ages 2 and 6 months of truncal hypotonia, athetosis, seizures, and ophthalmologic abnormalities, particularly optic atrophy and retinal degeneration.

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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