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Human Disease
Cayman type cerebellar ataxia
- Term ID
- DOID:0060694
- Synonyms
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- 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
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- ICD10CM:G11.0
- MESH:C563363
- MIM:601238
- ORDO:94122
- Ontology
- Human Disease ( DOID:0060694 )
- is a type of
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Genes Involved
Zebrafish Models