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

• GARD:9976
• OMIM:607458

Ontology

Human Disease   ( DOID:0050969 )