Disease_Mapped_To_Gene
Neonatal Encephalopathy
Severe Neonatal Encephalopathy Due to MECP2 Mutations
An X-linked recessive condition caused by mutation(s) in the MECP2 gene, encoding methyl-CpG-binding protein 2. It is characterized by severe neonatal encephalopathy.
C132293
C1968556
Cellosaurus
Disease or Syndrome
Severe Neonatal Encephalopathy Due to MECP2 Mutations
Severe Neonatal Encephalopathy Due to MECP2 Mutations
Cellosaurus Disease Terminology
Cellosaurus Terminology
MECP2 Gene