OBO ID: DOID:0050971
Term Name: spinocerebellar ataxia type 20 Search Ontology:
Synonyms:
Definition: An autosomal dominant cerebellar ataxia that is characterized by cerebellar dysarthria. https://rarediseases.info.nih.gov/diseases/9997/spinocerebellar-ataxia-20
References:
Ontology: Human Disease   ( DOID:0050971 )
Relationships
is a type of:
OTHER spinocerebellar ataxia type 20 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS (1)
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