Search Ontology:
Human Disease

autosomal recessive spinocerebellar ataxia 25

Term ID
DOID:0080259
Synonyms
  • SCAR25
Definition
An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the ATG5 gene on chromosome 6q21. https://www.ncbi.nlm.nih.gov/pubmed/26812546
References
Ontology
Human Disease   ( DOID:0080259 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models