disease has basis in dysfunction of WDR35 short-rib thoracic dysplasia 7 with or without polydactyly An asphyxiating thoracic dystrophy that has material basis in homozygous or compound heterozygous mutation in the WDR35 gene on chromosome 2p21.1. DOID:0110090 ICD10:Q77.2 MONDO:0013569 OMIM:614091 SRPS5 SRTD7 UMLS:C3279792 short rib-polydactyly syndrom type V short rib-polydactyly syndrome, type 5 short-rib thoracic dysplasia 7 with or without polydactyly Jeune syndrome short rib-polydactyly syndrome, Verma-Naumoff type