Charlevoix-Saguenay spastic ataxia

Summary
Definition
An autosomal recessive cerebellar ataxia that is characterized by early onset of cerebellar ataxia, pyramidal tract signs and peripheral neuropathy, has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding the sacsin protein on chromosome 13q12.
Super Class
autosomal recessive cerebellar ataxia
Disease Ontology
DOID:0050946
Mondo Disease Ontology
MeSH
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
26278 SACS sacsin molecular chaperone
51479 ANKFY1 ankyrin repeat and FYVE domain containing 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
50720 Sacs sacsin

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024