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| Term | autosomal dominant cerebellar ataxia | ID (Ontology) | DOID:1441 (Human Disease) | |||||||||||||||||||||||||||
| Definition | A cerebellar ataxia that has_material_basis_in autosomal dominant inheritance. | |||||||||||||||||||||||||||||
| Also Known As | "spinocerebellar ataxia" | |||||||||||||||||||||||||||||
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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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| Is a |
autosomal dominant disease cerebellar ataxia |
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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MESH:D020754 MIM:PS164400 NCI:C82341 ORDO:94 SNOMEDCT_US_2023_03_01:129609000 UMLS_CUI:C0087012 |
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