OBO ID: DOID:0050969
Term Name: spinocerebellar ataxia type 18 Search Ontology:
Synonyms:
Definition: An autosomal dominant cerebellar ataxia that is characterized by cerebellar ataxia and sensory neuropathy, has_material_basis_in mutation on chromosome 7q22-q23. https://rarediseases.info.nih.gov/diseases/9976/spinocerebellar-ataxia-18
References:
Ontology: Human Disease   ( DOID:0050969 )
Relationships
is a type of:
OTHER spinocerebellar ataxia type 18 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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