epilepsy, progressive myoclonic 3, with or without intracellular inclusions Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/611726
Similar Terms
Downloads & Tools

Genes

1 genes associated with the epilepsy, progressive myoclonic 3, with or without intracellular inclusions phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
KCTD7 potassium channel tetramerization domain containing 7