OBO ID: DOID:0050955
Term Name: spinocerebellar ataxia type 2 Search Ontology:
Synonyms:
Definition: An autosomal dominant cerebellar ataxia that is characterized by ataxia, bulbar palsy, peripheral neuropathy chorea and muscle atrophy, has_material_basis_in mutation in the ATXN2 gene. https://ghr.nlm.nih.gov/condition/spinocerebellar-ataxia-type-2
References:
Ontology: Human Disease   ( DOID:0050955 )
Relationships
is a type of:
OTHER spinocerebellar ataxia type 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ATXN2 Spinocerebellar ataxia 2 183090
{Amyotrophic lateral sclerosis, susceptibility to, 13} 183090
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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