epileptic encephalopathy, early infantile, 25 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/615905
Similar Terms
Downloads & Tools

Genes

1 genes associated with the epileptic encephalopathy, early infantile, 25 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SLC13A5 solute carrier family 13 (sodium-dependent citrate transporter), member 5