spinal muscular atrophy neuronopathy, distal hereditary motor, autosomal recessive 3 https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/neuronopathy_distal_hereditary_motor_autosomal_recessive_3 spinal muscular atrophy, distal, autosomal recessive, 3 distal hereditary motor neuropathy type 3 and type 4 autosomal recessive distal spinal muscular atrophy type 3 GARD:0016956 distal spinal muscular atrophy type 3 MONDO:0011771 MESH:C564626 MEDGEN:337659 Orphanet:139547 spinal muscular atrophy, chronic distal, autosomal recessive A rare neuromuscular disease characterized by progressive muscular weakness and atrophy predominantly affecting distal parts of limbs, later involvement of proximal and trunk muscles with marked hyperlordosis and late diaphragmatic dysfunction. DOID:0111211 dHMN3 and dHMN4 UMLS:C1846823 OMIM:607088 dSMA3 neuronopathy, distal hereditary motor, autosomal recessive