convulsions, familial infantile, with paroxysmal choreoathetosis Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/602066
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Genes

1 genes associated with the convulsions, familial infantile, with paroxysmal choreoathetosis phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
PRRT2 proline-rich transmembrane protein 2