spinocerebellar ataxia 45

Term ID

DOID:0080287

Synonyms

Definition

An autosomal dominant cerebellar ataxia that has_material_basis_in heterozygous mutation in the FAT2 gene on chromosome 5q33. https://pubmed.ncbi.nlm.nih.gov/29053796/

References

• OMIM:617769

Ontology

Human Disease   ( DOID:0080287 )