Search Ontology:
Human Disease

spinocerebellar ataxia type 18

Term ID
DOID:0050969
Synonyms
Definition
An autosomal dominant cerebellar ataxia that is characterized by cerebellar ataxia and sensory neuropathy, has_material_basis_in mutation on chromosome 7q22-q23. https://rarediseases.info.nih.gov/diseases/9976/spinocerebellar-ataxia-18
References
Ontology
Human Disease   ( DOID:0050969 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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