Disease

Cayman type 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.
Synonyms
  • Cayman cerebellar ataxia
Cross References
Parent Terms
Child Terms
None
Sources of Associations

Associated Genes

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Associated Models