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MIM:613402 - MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY; MCSZ
Echinobase Genes: pnkp
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 |