episodic ataxia, type 7 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Episodic ataxia type 7 (EA7) is an exceedingly rare form of Hereditary episodic ataxia (see this term) characterized by ataxia with weakness, vertigo, and dysarthria without interictal findings. (Orphanet Rare Disease Ontology, Orphanet_209970)
External Link http://www.omim.org/entry/611907
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1 genes associated with the episodic ataxia, type 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
EA7 Episodic ataxia, type 7