An asphyxiating thoracic dystrophy that has material basis in homozygous or compound heterozygous mutation in the DYNC2H1 gene on chromosome 11q22. The disease is MONDO_0013127 (asphyxiating thoracic dystrophy 3). Also known as: ATD3, DYNC2H1-related short rib thoracic dysplasia, SRPS type 1, SRPS type 3, SRPS1, SRPS2B, SRPS3, SRTD3.