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| Term | autosomal dominant cerebellar ataxia, deafness and narcolepsy | ID (Ontology) | DOID:0050968 (Human Disease) |
| 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. | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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No relevant statements available
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autosomal dominant disease__ cerebellar ataxia___________| autosomal dominant cerebellar ataxia |__autosomal dominant cerebellar ataxia, deafness and narcolepsy |
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| Is a | autosomal dominant cerebellar ataxia | ||
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External Crossreferences & Linkouts
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GARD:12372 MIM:604121 |
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