Search Ontology:
Human Disease

Cayman type cerebellar ataxia

Term ID
DOID:0060694
Synonyms
  • Cayman cerebellar ataxia
Definition
An autosomal recessive cerebellar ataxia characterized by marked autosomal recessive inheritance, psychomotor retardation, cerebellar dysfunction including nystagmus, intention tremor, dysarthria, and wide-based ataxic gait, hypotonia and the absence of retinal abnormalities that has_material_basis_in mutation in the ATCAY gene on chromosome 19p13.3. (2)
References
Ontology
Human Disease   ( DOID:0060694 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models