|OBO ID: DOID:0050994|
|Term Name:||episodic ataxia type 6||Search Ontology:|
|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. https://www.omim.org/entry/612656|
|Ontology:||Human Disease (DOID:0050994)|
|is a type of:||
OTHER episodic ataxia type 6 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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