MYOCLONIC EPILEPSY, FAMILIAL INFANTILE Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=OMIM:605021
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Genes

2 genes/proteins associated with the disease MYOCLONIC EPILEPSY, FAMILIAL INFANTILE from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
EIM Infantile myoclonic epilepsy 2.88009
TBC1D24 TBC1 domain family, member 24 2.88009