Phenotypes for disease #00202 (SGS (Shprintzen-Goldberg craniosynostosis syndrome (SGS)), OMIM:182212)

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0000039756 craniosynostosis; dolichocephaly; hypertelorism; down-slanting eyes; proptosis; malar hypoplasia; high/narrow palate; micrognathia; low set ears; arachnodactyly; camptodactyly; scoliosis; pectus deformity; joint hypermobility; joint contracture; no C1/2 spine malformation; hypotonia; developmental delay; mitral valve prolapse; aortic root dilatation; dural ectasia; no ectopia lentis; no cleft palate; no cleft palate; no club foot deformity; no arterial tortuosity; splenic artery aneurysm - - Isolated (sporadic) 43y - - - - Johan den Dunnen 00053031
0000039757 craniosynostosis; dolichocephaly; hypertelorism; down-slanting eyes; noproptosis; malar hypoplasia; high/narrow palate; micrognathia; low set ears; arachnodactyly; camptodactyly; scoliosis; pectus deformity; joint hypermobility; joint contracture; no C1/2 spine malformation; hypotonia; developmental delay; mitral valve prolapse; aortic root dilatation; dural ectasia; no ectopia lentis; no cleft palate; broad/bifid uvula; no club foot deformity; no arterial tortuosity; no other aneurysm - - Isolated (sporadic) 6y - - - - Johan den Dunnen 00053032
0000039758 craniosynostosis; dolichocephaly; hypertelorism; down-slanting eyes; proptosis; malar hypoplasia; high/narrow palate; micrognathia; low set ears; arachnodactyly; camptodactyly; scoliosis; pectus deformity; joint hypermobility; joint contracture; hypotonia; developmental delay; mitral valve prolapse; aortic root dilatation; no ectopia lentis; no cleft palate; club foot deformity - - Isolated (sporadic) 16y - - - - Johan den Dunnen 00053033
0000039759 craniosynostosis; dolichocephaly; hypertelorism; down-slanting eyes; proptosis; malar hypoplasia; high/narrow palate; micrognathia; low set ears; arachnodactyly; camptodactyly; scoliosis; pectus deformity; joint hypermobility; joint contracture; C1/2 spine malformation; hypotonia; developmental delay; no mitral valve prolapse; aortic root dilatation; no ectopia lentis; cleft palate; no cleft palate; no club foot deformity; no arterial tortuosity; no other aneurysm - - Isolated (sporadic) 12y - - - - Johan den Dunnen 00053034
0000039760 craniosynostosis; dolichocephaly; hypertelorism; down-slanting eyes; proptosis; malar hypoplasia; high/narrow palate; micrognathia; low set ears; arachnodactyly; camptodactyly; scoliosis; pectus deformity; joint hypermobility; joint contracture; C1/2 spine malformation; hypotonia; developmental delay; no mitral valve prolapse; aortic root dilatation; no ectopia lentis; no cleft palate; no club foot deformity - - Isolated (sporadic) 22y - - - - Johan den Dunnen 00053035
0000039761 craniosynostosis; dolichocephaly; hypertelorism; down-slanting eyes; noproptosis; malar hypoplasia; high/narrow palate; micrognathia; low set ears; arachnodactyly; camptodactyly; scoliosis; pectus deformity; joint hypermobility; joint contracture; hypotonia; developmental delay; aortic root dilatation; no ectopia lentis; no cleft palate - - Isolated (sporadic) 21y - - - - Johan den Dunnen 00053036
0000039762 craniosynostosis; no dolichocephaly; hypertelorism; down-slanting eyes; proptosis; malar hypoplasia; high/narrow palate; micrognathia; low set ears; arachnodactyly; no camptodactyly; scoliosis; pectus deformity; joint hypermobility; no joint contracture; hypotonia; developmental delay; aortic root dilatation; no ectopia lentis; cleft palate; no club foot deformity - - Isolated (sporadic) 2y - - - - Johan den Dunnen 00053037
0000039763 craniosynostosis; dolichocephaly; hypertelorism; down-slanting eyes; proptosis; malar hypoplasia; high/narrow palate; micrognathia; low set ears; arachnodactyly; no camptodactyly; no scoliosis; no pectus deformity; joint hypermobility; joint contracture; hypotonia; developmental delay; no mitral valve prolapse; no aortic root dilatation; no ectopia lentis; cleft palate; club foot deformity; splenic artery aneurysm with spontaneous rupture (blank cells, not determined) - - Isolated (sporadic) 6y - - - - Johan den Dunnen 00053038
0000039764 craniosynostosis; dolichocephaly; hypertelorism; down-slanting eyes; proptosis; malar hypoplasia; high/narrow palate; micrognathia; low set ears; arachnodactyly; camptodactyly; no scoliosis; pectus deformity; joint hypermobility; joint contracture; C1/2 spine malformation; hypotonia; developmental delay; mitral valve prolapse; no aortic root dilatation; no ectopia lentis; no cleft palate; no broad/bifid uvula; no club foot deformity - - Isolated (sporadic) 5y - - - - Johan den Dunnen 00053039
0000039765 craniosynostosis; dolichocephaly; hypertelorism; down-slanting eyes; proptosis; malar hypoplasia; high/narrow palate; micrognathia; low set ears; arachnodactyly; camptodactyly; scoliosis; pectus deformity; joint hypermobility; joint contracture; C1/2 spine malformation; hypotonia; developmental delay; mitral valve prolapse; aortic root dilatation; dural ectasia; no ectopia lentis; no cleft palate; broad/bifid uvula; no club foot deformity; arterial tortuosity; no other aneurysm - - Isolated (sporadic) 4y - - - - Johan den Dunnen 00053040
0000039766 craniosynostosis, no arachnodactyly, pectus deformity, no scoliosis, joint contractures, camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, no hernias, loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, no myopia - - Isolated (sporadic) 21y - - - - Johan den Dunnen 00053041
0000039768 no craniosynostosis, arachnodactyly, pectus deformity, scoliosis, joint contractures, no camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, no hernias, no loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, myopia - - Familial, autosomal dominant 42y - - - - Johan den Dunnen 00053043
0000039769 craniosynostosis, arachnodactyly, pectus deformity, scoliosis, joint contractures, no camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, hernias, loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, myopia - - Familial, autosomal dominant 22y - - - - Johan den Dunnen 00053044
0000039770 craniosynostosis, arachnodactyly, pectus deformity, scoliosis, joint contractures, camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, no hernias, no loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, no myopia - - Isolated (sporadic) 20y - - - - Johan den Dunnen 00053045
0000039771 no craniosynostosis, arachnodactyly, no pectus deformity, scoliosis, joint contractures, no camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, no proptosis, downslanting palpebral fissures, no micrognathia/retrognathia, intellectual disability, no hernias, no loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, myopia - - Familial, autosomal dominant 11y - - - - Johan den Dunnen 00053046
0000039772 no craniosynostosis, arachnodactyly, no pectus deformity, scoliosis, joint contractures, no camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, no hernias, no loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, myopia; 44y-died of respiratory insufficiency - - Familial, autosomal dominant 44y - - - - Johan den Dunnen 00053047
0000039773 no craniosynostosis, arachnodactyly, no pectus deformity, no scoliosis, joint contractures, no camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, downslanting palpebral fissures, no micrognathia/retrognathia, intellectual disability, no hernias, no loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, myopia - - Familial, autosomal dominant 13y - - - - Johan den Dunnen 00053048
0000039774 no craniosynostosis, arachnodactyly, no pectus deformity, scoliosis, joint contractures, no camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, no proptosis, downslanting palpebral fissures, no micrognathia/retrognathia, intellectual disability, no hernias, no loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, no myopia - - Familial, autosomal dominant 14y - - - - Johan den Dunnen 00053049
0000039775 craniosynostosis, arachnodactyly, pectus deformity, scoliosis, joint contractures, no camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, hernias, loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, myopia - - Familial, autosomal dominant 22y - - - - Johan den Dunnen 00053050
0000039776 craniosynostosis, arachnodactyly, pectus deformity, scoliosis, joint contractures, no camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, no proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, hernias, no loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, myopia? - - Familial, autosomal dominant 20y - - - - Johan den Dunnen 00053051
0000039777 craniosynostosis, arachnodactyly, pectus deformity, scoliosis, no joint contractures, no camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, hernias, no loss of subcutaneous fat, mitral valve prolapse, aortic dilatation requiring surgery (16y, aortic root dilatation with Z score=7.014), vertebrobasilar and internal carotid tortuosity, dilated pulmonary-artery root, no myopia - - Isolated (sporadic) 18y - - - - Johan den Dunnen 00053052
0000039778 craniosynostosis, arachnodactyly, pectus deformity, scoliosis, joint contractures, camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, no proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, no hernias, loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, no myopia - - Isolated (sporadic) 16y - - - - Johan den Dunnen 00053053
0000039779 no craniosynostosis, arachnodactyly, pectus deformity, no scoliosis, no joint contractures, no camptodactyly, no foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, hernias, no loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, no myopia - - Isolated (sporadic) 5y - - - - Johan den Dunnen 00053054
0000039780 craniosynostosis, arachnodactyly, pectus deformity, scoliosis, joint contractures, camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, hernias, loss of subcutaneous fat, mitral valve prolapse, no aortic root dilatation, no myopia - - Isolated (sporadic) 21y - - - - Johan den Dunnen 00053055
0000039781 craniosynostosis, arachnodactyly, pectus deformity, scoliosis, joint contractures, camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, no downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, hernias, loss of subcutaneous fat, mitral valve prolapse, mitral insufficiency, aortic root dilatation upper normal limit, myopia; 10y died suddenly, autopsy showed severe mitral valve dysplasia with calcifications mitral annulus - - Isolated (sporadic) 10y - - - - Johan den Dunnen 00053056
0000039782 craniosynostosis, arachnodactyly, pectus deformity, scoliosis, joint contractures, camptodactyly, foot malposition, no scaphocephaly/dolichocephaly, no hypertelorism, proptosis, downslanting palpebral fissures, no micrognathia/retrognathia, intellectual disability, hernias, no loss of subcutaneous fat, mitral valve prolapse, aortic root dilatation, no myopia - - Isolated (sporadic) 11y - - - - Johan den Dunnen 00053057
0000039783 no craniosynostosis, arachnodactyly, pectus deformity, scoliosis, no joint contractures, camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, hernias, no loss of subcutaneous fat, mitral valve prolapse, mitral insufficiency, aortic root dilatation, myopia - - Isolated (sporadic) 32y - - - - Johan den Dunnen 00053058
0000039784 craniosynostosis, arachnodactyly, pectus deformity, scoliosis, joint contractures, camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, no downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, hernias, loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, no myopia - - Isolated (sporadic) 20y - - - - Johan den Dunnen 00053059
0000039785 craniosynostosis, arachnodactyly, pectus deformity, scoliosis, no joint contractures, camptodactyly, no foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, no downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, hernias, no loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, no myopia - - Familial, autosomal dominant 26y - - - - Johan den Dunnen 00053060
0000230406 Scoliosis (HP:0002650), Bifid uvula (HP:0000193), Wide anterior fontanel (HP:0000260) Shprintzen-Goldberg syndrome SGS Isolated (sporadic) 3m - - - - Katta M Girisha 00303329
0000299892 Proptosis, Generalized hypotonia, Dystonia, Plagiocephaly, Failure to thrive, Scoliosis - - Unknown 00y06m - - - - Andreas Laner 00407762
0000309911 see paper (extensive phenotyping) Shprintzen-Goldberg craniosynostosis syndrome SGS Familial, autosomal dominant - - - - - Johan den Dunnen 00418574
0000309912 see paper (extensive phenotyping) Shprintzen-Goldberg craniosynostosis syndrome SGS Familial, autosomal dominant - - - - - Johan den Dunnen 00418575
0000309913 see paper (extensive phenotyping) Shprintzen-Goldberg craniosynostosis syndrome SGS Familial, autosomal dominant - - - - - Johan den Dunnen 00418576
0000309914 see paper (extensive phenotyping) Shprintzen-Goldberg craniosynostosis syndrome SGS Familial, autosomal dominant - - - - - Johan den Dunnen 00418577
0000310070 hypermetropy, joint hypermobility, mitral valve prolapse, polyvalvular dysplasia/ insufficiency, kyphoscoliosis , bilateral inguinal hernias Aortic valvular disease Shprintzen–Goldberg Syndrome Unknown - - - - - Carmela Fusco 00418774
0000310071 mitral valve prolapse, aneurismatic ovale fossa, megalocornea, joint hypermobility, Intellectual disability Aortic valvular disease Shprintzen–Goldberg Syndrome Familial - - - - - Carmela Fusco 00418775
0000343212 Hypotonia, Mild global developmental delay, Pectus excavatum, Scapular winging, Atrial septal defect, Mildly elevated creatine kinase, Oligohydramnios - - Isolated (sporadic) 08y - - - - Andreas Laner 00454565
0000350492 Intellectual disability, Delayed speech and language development, Obesity, Brachycephaly, Anteverted nares, Synophrys, Abnormal dental enamel morphology, Short stature, Microcephaly, Neurodevelopmental delay - - Unknown 13y - - - - Andreas Laner 00464463
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