autosomal recessive spinocerebellar ataxia 15

Term ID

DOID:0080057

Synonyms

• SCAR15

Definition

An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the RUBCN gene on chromosome 3q29. https://www.ncbi.nlm.nih.gov/pubmed/20826435

References

• OMIM:615705

Ontology

Human Disease   ( DOID:0080057 )