asphyxiating thoracic dystrophy 3 ATD3 An asphyxiating thoracic dystrophy that has material basis in homozygous or compound heterozygous mutation in the DYNC2H1 gene on chromosome 11q22. DOID:0110087 ICD10:Q77.2 MONDO:0013127 NCIT:C163755 OMIM:613091 SRPS1 SRPS2B SRPS3 SRTD3 Saldino-Noonan syndrome Verma-Naumoff syndrome asphyxiating thoracic dystrophy 3 asphyxiating thoracic dystrophy type 3 polydactyly with neonatal chondrodystrophy, type 1 polydactyly with neonatal chondrodystrophy, type 3 polydactyly with neonatal chondrodystrophy, type I polydactyly with neonatal chondrodystrophy, type III short rib-polydactyly syndrome, type 1 short rib-polydactyly syndrome, type 2B short rib-polydactyly syndrome, type 3 short rib-polydactyly syndrome, type I short rib-polydactyly syndrome, type IIB short-rib thoracic dysplasia 3 with or without polydactyly Jeune syndrome short rib-polydactyly syndrome, Majewski type short rib-polydactyly syndrome, Verma-Naumoff type