autosomal recessive spinocerebellar ataxia 21

Summary
Synonym
  • SCAR21
  • acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome
  • autosomal recessive spinocerebellar ataxia 21 with hepatopathy
Definition
An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the SCYL1 gene on chromosome 11q13.
Super Class
autosomal recessive cerebellar ataxia
Disease Ontology
DOID:0111155
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
57410 SCYL1 SCY1 like pseudokinase 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
854279 CEX1 Cex1p

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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