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Human Disease

spinocerebellar ataxia type 37

Term ID
DOID:0050984
Synonyms
Definition
An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia and dysarthria, presenting in mid-adulthood, and has_material_basis_in mutation to the DAB1 gene. https://www.omim.org/entry/615945
References
Ontology
Human Disease   ( DOID:0050984 )
Relationships
is a type of
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Genes Involved
Zebrafish Models