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Disease Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations

Name Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations
Synonym Mecp2-Related Severe Neonatal Encephalopathy
Categories Genetic disease (inborn) | Nervous system disease
MeSH® ID C566878
OMIM® ID 300673

Top ↑ Ancestors

1. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Neurologic Manifestations Has associated chemicals Has associated genes Has associated exposure references Neurobehavioral Manifestations Has associated chemicals Has associated genes Has associated exposure references Intellectual Disability Has associated chemicals Has associated genes Has associated exposure references Mental Retardation, X-Linked Has associated chemicals Has associated genes Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Has associated chemicals Has associated genes
2. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, X-Linked Has associated chemicals Has associated genes Mental Retardation, X-Linked Has associated chemicals Has associated genes Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Has associated chemicals Has associated genes
3. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Heredodegenerative Disorders, Nervous System Has associated chemicals Has associated genes Mental Retardation, X-Linked Has associated chemicals Has associated genes Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Has associated chemicals Has associated genes

Top ↑ Descendants

None.