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| Term | episodic ataxia type 6 | ID (Ontology) | DOID:0050994 (Human Disease) | |||||||||||||||||||||||||||
| Definition | An episodic ataxia that is characterized by nystagmus and dysarthria, and has_material_basis_in autosomal dominant inheritance of mutation in the SLC1A3 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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hereditary ataxia |__episodic ataxia |__episodic ataxia type 6 21 rec. |
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| Is a | episodic ataxia | ||
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External Crossreferences & Linkouts
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| MIM:612656 | |||