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Disease Spinocerebellar ataxia 21

Name Spinocerebellar ataxia 21
Synonym SCA21
Categories Genetic disease (inborn) | Nervous system disease
MeSH® ID C537200
OMIM® ID 607454

Top ↑ Ancestors

1. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Central Nervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Brain Diseases Has associated chemicals Has associated genes Has associated exposure references Cerebellar Diseases Has associated chemicals Has associated genes Spinocerebellar Degenerations Has associated chemicals Has associated genes Spinocerebellar ataxia 21
2. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Central Nervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Spinal Cord Diseases Has associated chemicals Has associated genes Has associated exposure references Spinocerebellar Degenerations Has associated chemicals Has associated genes Spinocerebellar ataxia 21
3. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Neurodegenerative Diseases Has associated chemicals Has associated genes Has associated exposure references Heredodegenerative Disorders, Nervous System Has associated chemicals Has associated genes Spinocerebellar Degenerations Has associated chemicals Has associated genes Spinocerebellar ataxia 21
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 Heredodegenerative Disorders, Nervous System Has associated chemicals Has associated genes Spinocerebellar Degenerations Has associated chemicals Has associated genes Spinocerebellar ataxia 21

Top ↑ Descendants

None.