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

• OMIM:615945

Ontology

Human Disease   ( DOID:0050984 )