Search Ontology:
Human Disease

autosomal recessive spinocerebellar ataxia 11

Term ID
DOID:0080063
Synonyms
  • SCAR11
Definition
An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the SYT14 gene on chromosome 1q32. https://www.ncbi.nlm.nih.gov/pubmed/21835308
References
Ontology
Human Disease   ( DOID:0080063 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models