severe neonatal-onset encephalopathy with microcephaly (Q55782469)
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human disease
- Severe congenital encephalopathy due to MECP2 mutation
- ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
- severe congenital encephalopathy due to MECP2 mutation
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | severe neonatal-onset encephalopathy with microcephaly |
human disease |
|
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C132293
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