Episodic ataxia, type 6 Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Episodic ataxia type 6 (EA6) is an exceedingly rare form of Hereditary episodic ataxia (see this term) with varying degrees of ataxia and associated findings including slurred speech, headache, confusion and hemiplegia. (Orphanet Rare Disease Ontology, Orphanet_209967)
External Link http://www.omim.org/entry/612656
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1 genes associated with the Episodic ataxia, type 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
SLC1A3 solute carrier family 1 (glial high affinity glutamate transporter), member 3