Search Ontology:
Human Disease

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
Ontology
Human Disease   ( DOID:0080287 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models