| C1968556 |
ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS |
MONDO |
severe neonatal-onset encephalopathy with microcephaly
|
0010397 |
| C1968556 |
ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS |
MSH |
Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations
|
C566878 |
| C1968556 |
ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS |
NCI |
Severe Neonatal Encephalopathy Due to MECP2 Mutations
|
C132293 |
| C1968556 |
ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS |
OMIM |
ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
|
300673 |
| C1968556 |
ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS |
ORDO |
Severe neonatal-onset encephalopathy with microcephaly
|
209370 |