OBO ID: DOID:0050956
Term Name: spinocerebellar ataxia type 6 Search Ontology:
Synonyms:
Definition: An autosomal dominant cerebellar ataxia that is characterized by progresive ataxia, has_material_basis_in mutation in the CACNA1A gene. https://ghr.nlm.nih.gov/condition/spinocerebellar-ataxia-type-6
References:
Ontology: Human Disease   ( DOID:0050956 )
Relationships
is a type of:
OTHER spinocerebellar ataxia type 6 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CACNA1A Spinocerebellar ataxia 6 183086
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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