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Human Disease

episodic ataxia type 2

Term ID
DOID:0050990
Synonyms
Definition
An episodic ataxia that is characterized by periodic ataxia and nystagmus, and has_material_basis_in autosomal dominant inheritance of mutation in the calcium channel gene CACNA1A. https://www.omim.org/entry/108500
References
Ontology
Human Disease   ( DOID:0050990 )
Relationships
is a type of
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Genes Involved
Zebrafish Models