autosomal recessive spinocerebellar ataxia 21 (DOID:0111155)
Alliance: disease page
Synonyms: acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome; autosomal recessive spinocerebellar ataxia 21 with hepatopathy; SCAR21
Alt IDs: OMIM:616719, ORDO:466794
Definition: An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the SCYL1 gene on chromosome 11q13.