OBO ID: DOID:0050962
Term Name: spinocerebellar ataxia type 12 Search Ontology:
Synonyms:
Definition: An autosomal dominant cerebellar ataxia that is characterized by minor ataxia and intention tremor, has_material_basis_in CAG expansion of the PPP2R2B gene. https://rarediseases.info.nih.gov/diseases/10476/spinocerebellar-ataxia-12
References:
Ontology: Human Disease   ( DOID:0050962 )
Relationships
is a type of:
OTHER spinocerebellar ataxia type 12 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PPP2R2B Spinocerebellar ataxia 12 604326
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.