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short rib-polydactyly syndrome (MONDO:0015461)
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syndromic anorectal malformation (MONDO:0015246)
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short rib-polydactyly syndrome, Verma-Naumoff type ()

       Child Nodes:
........expandasphyxiating thoracic dystrophy 3 ()
........expandshort-rib thoracic dysplasia 11 with or without polydactyly ()
........expandshort-rib thoracic dysplasia 7 with or without polydactyly ()
........expandshort-rib thoracic dysplasia 8 with or without polydactyly ()



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..expandcataract-intellectual disability-anal atresia-urinary defects syndrome ()
..expandcaudal duplication ()
..expandcaudal regression-sirenomelia spectrum ()
..expandcloacal exstrophy (disease) ()
..expandCurrarino triad ()
..expanddistal monosomy 13q ()
..expandDuane-radial ray syndrome ()
..expandeven-plus syndrome ()
..expandFG syndrome 1 ()
..expandFraser syndrome ()
..expandGoldberg-Shprintzen megacolon syndrome ()
..expandHirschsprung disease-deafness-polydactyly syndrome ()
..expandHirschsprung disease-ganglioneuroblastoma syndrome ()
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..expandHirschsprung disease-type D brachydactyly syndrome ()
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..expandmaternal uniparental disomy of chromosome 16 ()
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..expandOpitz G/BBB syndrome ()
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..expandpelvis syndrome ()
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..expandring chromosome 13 ()
..expandshort rib-polydactyly syndrome, Verma-Naumoff type ()
..expandskeletal dysplasia-intellectual disability syndrome ()
..expandspondylocostal dysostosis-anal and genitourinary malformations syndrome ()
..expandsyndactyly-telecanthus-anogenital and renal malformations syndrome ()
..expandtetrasomy 12p ()
..expandTownes-Brocks syndrome ()
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MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:19664
Name:short rib-polydactyly syndrome, Verma-Naumoff type
Definition:Short rib-polydactyly syndrome, Verma-Naumoff type is a short rib-polydactyly syndrome (see this term), characterized by short limb dwarfism, short ribs with thoracic dysplasia, postaxial polydactyly and protuberant abdomen. Associated multiple malformations include cardiovascular defects, renal agenesis /hypoplasia (see these terms), anormal clocal development (ambiguous genitalia, anal atresia) and cerebellar hypoplasia. Short rib-polydactyly syndrome, Verma-Naumoff type follows an autosomal recessive mode of transmission. The disease is usually fatal in the perinatal period.
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Synonyms:polydactyly with neonatal chondrodystrophy type III; short rib polydactyly syndrome Verma Naumoff type; short rib-polydactyly syndrome type 3; short rib-polydactyly syndrome type III; SRPS type 3; Verma Naumoff syndrome
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