autosomal dominant cerebellar ataxia, deafness and narcolepsy Disease Ontology Browser

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autosomal dominant cerebellar ataxia, deafness and narcolepsy (DOID:0050968)
Alliance: disease page
Alt IDs: OMIM:604121
Definition: An autosomal dominant cerebellar ataxia that is characterized by ataxia, sensorineal deafness, narcolepsy with cataplexy, and dementia, has_material_basis_in mutation in the DNMT1 gene.

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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