spinocerebellar ataxia type 19/22

Term ID

DOID:0050970

Synonyms

Definition

An autosomal dominant cerebellar ataxia that is characterized by mild cerebellar ataxia, cognitive impairment, myoclonus and tremor. https://rarediseases.info.nih.gov/diseases/12365/spinocerebellar-ataxia-19-and-22

References

• GARD:12365
• OMIM:607346

Ontology

Human Disease   ( DOID:0050970 )