| Dataset | DISEASES Curated Gene-Disease Association Evidence Scores |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A neuromuscular disease characterized by sporadic bouts of ataxia with or without continuous muscle movement. (Human Disease Ontology, DOID_963) |
| Similar Terms | |
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4 genes involed in the disease episodic ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
| Symbol | Name |
|---|---|
| CACNA1A | calcium channel, voltage-dependent, P/Q type, alpha 1A subunit |
| CACNB4 | calcium channel, voltage-dependent, beta 4 subunit |
| KCNA1 | potassium channel, voltage gated shaker related subfamily A, member 1 |
| SLC1A3 | solute carrier family 1 (glial high affinity glutamate transporter), member 3 |
