FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Cayman type cerebellar ataxia ID (Ontology) DOID:0060694 (Human Disease)
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.
Also Known As "Cayman cerebellar ataxia"
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 Cayman type cerebellar ataxia       1
 for disease ribbon | Cayman type cerebellar ataxia       1
 model of | Cayman type cerebellar ataxia       1
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autosomal recessive disease__
cerebellar ataxia____________|
                             autosomal recessive cerebellar ataxia
                              |__Cayman type cerebellar ataxia  1 rec.
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Is a autosomal recessive cerebellar ataxia
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Synonyms
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Secondary IDs
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ICD10CM:G11.0
MESH:C563363
MIM:601238
ORDO:94122