disease has basis in dysfunction of DYNC2I1 short-rib thoracic dysplasia 8 with or without polydactyly An asphyxiating thoracic dystrophy that has material basis in compound heterozygous mutation in the WDR60 gene on chromosome 7q36. DOID:0110094 ICD10:Q77.2 MONDO:0014214 OMIM:615503 SRPS6 SRTD8 UMLS:C3809691 short rib-polydactyly syndrome type VI short rib-polydactyly syndrome, type 6 short-rib thoracic dysplasia 8 with or without polydactyly Jeune syndrome short rib-polydactyly syndrome, Verma-Naumoff type