ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS

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Summary

Literature (0)

MIM:300673 - ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS

Xenbase Genes: mecp2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010397 - severe neonatal-onset encephalopathy with microcephaly

MONDO:0010397 - severe neonatal-onset encephalopathy with microcephaly

Disease Ontology (DO):

DOID:0111932 - severe congenital encephalopathy due to MECP2 mutation

DOID:0111932 - severe congenital encephalopathy due to MECP2 mutation