Neurogenic arthrogryposis multiplex congenita is a form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. The disease is arthrogryposis multiplex congenita 2, neurogenic type (MONDO_0008823, a Monarch Disease Ontology identifier). Also known as: AMC neurogenic type, AMCN, arthrogryposis multiplex congenita neurogenic type, neurogenic arthrogryposis multiplex congenita.