autosomal recessive intellectual developmental disorder neurodevelopmental disorder with cerebellar atrophy and motor dysfunction MIM:619333 disease_ontology MIM:619333 An autosomal recessive intellectual developmental disorder characterized by cerebellar atrophy and global developmental delay with cognitive impairment, speech delay, and prominent motor abnormalities including axial hypotonia, gait ataxia, and appendicular spasticity that has_material_basis_in homozygous or compound heterozygous mutation in the GEMIN5 gene on chromosome 5q33.2. DOID:0070443