Search Ontology:
Human Disease

spinocerebellar ataxia type 25

Term ID
DOID:0050974
Synonyms
Definition
An autosomal dominant cerebellar ataxia that is characterized by ataxia and sensory neuropathy, has_material_basis_in repeat CAG expansion on chromosome 2p15-p21. https://rarediseases.info.nih.gov/diseases/9996/spinocerebellar-ataxia-25
References
Ontology
Human Disease   ( DOID:0050974 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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