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Disease RETT SYNDROME, CONGENITAL VARIANT

Name RETT SYNDROME, CONGENITAL VARIANT
Categories Genetic disease (inborn) | Nervous system disease
OMIM® ID 613454
External Links

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 Rett Syndrome Has associated chemicals Has associated genes RETT SYNDROME, CONGENITAL VARIANT 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 Rett Syndrome Has associated chemicals Has associated genes RETT SYNDROME, CONGENITAL VARIANT 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 Rett Syndrome Has associated chemicals Has associated genes RETT SYNDROME, CONGENITAL VARIANT Has associated chemicals Has associated genes

Top ↑ Descendants

None.