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OMIM:300673 - ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
MONDO:0010397 - severe neonatal-onset encephalopathy with microcephaly |
Human Disease Resources: OMIM
Xenbase Genes: mecp2
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MONDO:0010397 - severe neonatal-onset encephalopathy with microcephaly |