myoclonus, familial cortical Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/614937
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Genes

1 genes associated with the myoclonus, familial cortical phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
NOL3 nucleolar protein 3 (apoptosis repressor with CARD domain)