OBO ID: DOID:0050979
Term Name: spinocerebellar ataxia type 30 Search Ontology:
Synonyms:
Definition: An autosomal dominant cerebellar ataxia that is characterized by slowly progressive gait abnormalities and dysarthria, has_material_basis_in mutation in the ODZ3 gene. https://www.omim.org/entry/613371
References:
Ontology: Human Disease   ( DOID:0050979 )
Relationships
is a type of:
OTHER spinocerebellar ataxia type 30 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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