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| Term | spinocerebellar ataxia type 31 | ID (Ontology) | DOID:0050980 (Human Disease) | |||||||||||||||||||||||||||
| Definition | An autosomal dominant cerebellar ataxia that is characterized by late-onset ataxia, dysarthria and horizontal nystagmus, has_material_basis_in repeat expansion mutation in the BEAN1 gene. | |||||||||||||||||||||||||||||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal dominant disease__ cerebellar ataxia___________| autosomal dominant cerebellar ataxia |__spinocerebellar ataxia type 31 29 rec. |
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| Is a | autosomal dominant cerebellar ataxia | ||
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External Crossreferences & Linkouts
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| MIM:117210 | |||