disease has basis in dysfunction of IFT140 short-rib thoracic dysplasia 9 with or without polydactyly An asphyxiating thoracic dystrophy that has material basis in homozygous or compound heterozygous mutation in the IFT140 gene on chromosome 16p13. Conorenal syndrome DOID:0110097 GARD:0008600 ICD10:Q87.5 ICD9:759.89 MONDO:0009964 Mainzer Saldino syndrome Mainzer-Saldino syndrome OMIM:266920 Orphanet:140969 SCTID:254092004 SRTD9 Saldino-Mainzer syndrome renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, and skeletal dysplasia renal dysplasia-retinal pigmentary dystrophy-cerebellar ataxia-skeletal dysplasia syndrome short-rib thoracic dysplasia 9 with or without polydactyly Jeune syndrome acromelic dysplasia familial cystic renal disease syndromic retinitis pigmentosa retinal ciliopathy