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Human Disease

spinocerebellar ataxia type 7

Term ID
DOID:0050958
Synonyms
Definition
An autosomal dominant cerebellar ataxia that is characterized by ataxia, progressive vision loss, and failure to thrive, has_material_basis_in mutation in the ATXN7 gene. https://rarediseases.info.nih.gov/diseases/4955/spinocerebellar-ataxia-7
References
Ontology
Human Disease   ( DOID:0050958 )
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