OBO ID: DOID:0050970
Term Name: spinocerebellar ataxia type 19/22 Search Ontology:
Synonyms:
Definition: An autosomal dominant cerebellar ataxia that is characterized by mild cerebellar ataxia, cognitive impairment, myoclonus and tremor. https://rarediseases.info.nih.gov/diseases/12365/spinocerebellar-ataxia-19-and-22
References:
Ontology: Human Disease   ( DOID:0050970 )
Relationships
is a type of:
OTHER spinocerebellar ataxia type 19/22 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
KCND3 Spinocerebellar ataxia 19 607346
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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