OBO ID: DOID:0050973
Term Name: spinocerebellar ataxia type 23 Search Ontology:
Synonyms:
Definition: An autosomal dominnant cerebellar ataxia that is characterized by slowly progressive ataxia, dysarthria, slow saccades and hyperreflexia, has_material_basis_in mutation in the PDYN gene. https://rarediseases.info.nih.gov/diseases/9950/spinocerebellar-ataxia-23
References:
Ontology: Human Disease   ( DOID:0050973 )
Relationships
is a type of:
OTHER spinocerebellar ataxia type 23 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PDYN Spinocerebellar ataxia 23 610245
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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