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Disease Chromosome Xp11.3 Deletion Syndrome

Name Chromosome Xp11.3 Deletion Syndrome
Synonym Mental Retardation, X-Linked, With Retinitis Pigmentosa
Categories Eye disease | Genetic disease (inborn) | Nervous system disease
MeSH® ID C564481
OMIM® ID 300578

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 Chromosome Xp11.3 Deletion Syndrome Has associated chemicals Has associated genes
2. DiseasesEye Diseases Has associated chemicals Has associated genes Has associated exposure references Eye Diseases, Hereditary Has associated chemicals Has associated genes Retinitis Pigmentosa Has associated chemicals Has associated genes Chromosome Xp11.3 Deletion Syndrome Has associated chemicals Has associated genes
3. DiseasesEye Diseases Has associated chemicals Has associated genes Has associated exposure references Retinal Diseases Has associated chemicals Has associated genes Has associated exposure references Retinal Degeneration Has associated chemicals Has associated genes Has associated exposure references Retinal Dystrophies Has associated chemicals Has associated genes Retinitis Pigmentosa Has associated chemicals Has associated genes Chromosome Xp11.3 Deletion Syndrome Has associated chemicals Has associated genes
4. 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 Eye Diseases, Hereditary Has associated chemicals Has associated genes Retinitis Pigmentosa Has associated chemicals Has associated genes Chromosome Xp11.3 Deletion Syndrome Has associated chemicals Has associated genes
5. 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 Chromosome Xp11.3 Deletion Syndrome Has associated chemicals Has associated genes
6. 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 Chromosome Xp11.3 Deletion Syndrome Has associated chemicals Has associated genes

Top ↑ Descendants

None.