OBO ID: DOID:0050960
Term Name: spinocerebellar ataxia type 10 Search Ontology:
Synonyms:
Definition: An autosomal dominant cerebellar ataxia that is characterized by gait ataxia, upper-limb ataxia, dysarthria and dysphagia, has_material_basis_in mutation in the ATXN10 gene. https://www.ncbi.nlm.nih.gov/books/NBK1175/
References:
Ontology: Human Disease   ( DOID:0050960 )
Relationships
is a type of:
OTHER spinocerebellar ataxia type 10 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ATXN10 Spinocerebellar ataxia 10 603516
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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