Term Name:	autosomal recessive spinocerebellar ataxia 21
Synonyms:	acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome, autosomal recessive spinocerebellar ataxia 21 with hepatopathy, SCAR21
Definition:	An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the SCYL1 gene on chromosome 11q13.
Ontology:	Human Disease [DOID:0111155]   ( DOID:0111155 )