DO_rare_slim has material basis in autosomal recessive disease infection-induced acute-onset axonal neuropathy MIM:621333 A motor neuron disease characterized by acute onset of progressive muscle weakness and axonal sensorimotor neuropathy following an infection or febrile episode in infancy or early childhood that has_material_basis_in homozygous or compound heterozygous mutation in the RCC1 gene on chromosome 1p35. Affected individuals may have progressive cerebral and cerebellar atrophy and may have recurrent episodes resulting in loss of ambulation, long-term ventilatory support, or early death. IIAAN UMLS_CUI:C6065907 UMLS_CUI:C6065907 disease_ontology DOID:0070798 MIM:621333 motor neuron disease autosomal recessive inheritance