Term Name:	autosomal recessive spinocerebellar ataxia 31
Synonyms:	SCAR31
Definition:	An autosomal recessive cerebellar ataxia characterized by global developmental delay with hypotonia and variably impaired intellectual and language development that has_material_basis_in homozygous or compound heterozygous mutation in the ATG7 gene on chromosome 3p25.
Ontology:	Human Disease [DOID:0070412]   ( DOID:0070412 )