Term Name:	ataxia-telangiectasia-like disorder 1
Synonyms:
Definition:	An autosomal recessive cerebellar ataxia that is characterized clinically by progressive cerebellar degeneration resulting in ataxia and oculomotor apraxia and that has_material_basis_in homozygous or compound heterozygous mutation in the MRE11A gene (MRE11) on chromosome 11q21.
Ontology:	Human Disease [DOID:0081384]   ( DOID:0081384 )