Search Ontology:
Human Disease

spinocerebellar ataxia type 36

Term ID
DOID:0050983
Synonyms
Definition
An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria, hyperreflexia, sensiorineural hearing loss and muscle atrophy, has_material_basis_in mutation in the NOP56 gene. https://ghr.nlm.nih.gov/condition/spinocerebellar-ataxia-type-36
References
Ontology
Human Disease   ( DOID:0050983 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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