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MIM:613477 - EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5; EIEE5
Echinobase Genes: sptan1
Human Disease Resource: OMIM
DOID:0050709 - Ohtahara syndrome |
DOID:0080438 - developmental and epileptic encephalopathy 5 |
DOID:2481 - infantile epileptic encephalopathy |