disease has basis in dysfunction of ERGIC1 arthrogryposis multiplex congenita 2, neurogenic type AMC neurogenic type AMC, neurogenic type AMCN DOID:0090124 GARD:0000790 ICD10:Q74.3 MESH:C536614 MONDO:0008823 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. OMIM:208100 Orphanet:1143 SCTID:715316005 UMLS:C1859721 arthrogryposis multiplex congenita neurogenic type arthrogryposis multiplex congenita, neurogenic type neurogenic arthrogryposis multiplex congenita neurogenic type of AMC arthrogryposis multiplex congenita