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MIM:613722 - EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12; EIEE12
Echinobase Genes:
Human Disease Resource: OMIM
DOID:0050709 - Ohtahara syndrome |
DOID:2481 - infantile epileptic encephalopathy |
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DOID:0050709 - Ohtahara syndrome |
DOID:2481 - infantile epileptic encephalopathy |