myoclonic epilepsy, infantile, familial Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/605021
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Genes

1 genes associated with the myoclonic epilepsy, infantile, familial phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
TBC1D24 TBC1 domain family, member 24