autosomal recessive spinocerebellar ataxia 26

Term ID

DOID:0080260

Synonyms

• SCAR26

Definition

An autosomal recessive cerebellar ataxia that has_material_basis_in compound heterozygous mutation in the XRCC1 gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/28002403

References

• OMIM:617633

Ontology

Human Disease   ( DOID:0080260 )