Phenotypes for disease #01006 (KDVS (Koolen-De Vries syndrome (KDVS, 17q21.31 deletion syndrome)), OMIM:610443)

45 entries on 1 page. Showing entries 1 - 45.
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0000092541 Intrauterine growth retardation; hypotonia; failure to thrive in infancy; abnormal hair texture; broad forehead; sparse eyebrows; upslanting palpebral fissures; epicanthal folds; pear-shaped nose; large nasal bridge; bulbous nasal tip; long philtrum; everted lower lip; large and/or prominent ears; broad chin; motor delay; mild intellectual disability; happy, friendly disposition; joint hyperextensibility; recurrent otitis - - Isolated (sporadic) 3y - - - - Giuseppe Marangi 00117294
0000092542 Hypotonia; failure to thrive in infancy; abnormal hair texture; broad forehead; sparse eyebrows; long face; upslanting palpebral fissures; epicanthal folds; pear-shaped nose; large nasal bridge; bulbous nasal tip; long philtrum; large and/or prominent ears; broad chin; motor delay; moderate intellectual disability; happy, friendly disposition; dislocation of the hip; scoliosis; joint hyperextensibility; laryngospasm - - Isolated (sporadic) 14y - - - - Giuseppe Marangi 00117295
0000092543 microdeletion syndrome, chromosome 17q21.31; intrauterine growth retardation; birth weight 2,500 g (5th centile); feeding difficulties, stridor, and failure to thrive in infancy; hypotonia; global developmental delay; independent walking and first words at two years of age; impaired fine motor skills; no seizures or stereotypical movements; short stature; fair hair; upslanting palpebral fissures; epicanthic folds; telecanthus; broad nasal base; smooth philtrum; thin vermillion border; small teeth; short webbed neck; blind ending sacral dimple; pes planus; prominence of the lateral ventricles secondary to lack of white matter volume, and some heterotopic nodules in the right frontal horn at brain MRI. - - Isolated (sporadic) 2y11m - - - - Giuseppe Marangi 00117296
0000092544 bilateral cleft lip and palate; micrognathia; ventricular septal defect (VSD) spontaneously resolved; cryptorchidism; sacral dimple; neonatal hypotonia, inspiratory stridor and feeding difficulties; developmental delay, with independent walking at 26 months, and first words at 18 months; expressive language disorder; moderate cognitive impairment (IQ 35); friendly personality; normal brain MRI; frequent acute otitis media; mild hypermetropia; strabismus divergens; long face; micrognathia; hypertelorism; strabismus; everted ears; short upslanting palpebral fissures; high nasal bridge; broad pear-shaped nose; long philtrum; open mouth appearance; unilateral simian crease; scoliosis; pes planus; mild hypotonia; gait instability - - Isolated (sporadic) 13y - - - - Giuseppe Marangi 00117297
0000092545 microdeletion syndrome, chromosome 17q21.31 - - Isolated (sporadic) - - - - - Johan den Dunnen 00117298
0000092546 microdeletion syndrome, chromosome 17q21.31 - - Isolated (sporadic) - - - - - Johan den Dunnen 00117299
0000092547 Koolen-de Vries syndrome see paper … - - Isolated (sporadic) 3y4m - - - - David Koolen 00117329
0000092548 Koolen-de Vries syndrome see paper … - - Isolated (sporadic) 5y7m - - - - David Koolen 00117330
0000092549 Koolen-de Vries syndrome see paper … - - Isolated (sporadic) 6y - - - - David Koolen 00117331
0000092550 Koolen-de Vries syndrome see paper … - - Isolated (sporadic) 06y02m - - - - David Amor 00117332
0000092551 Koolen-de Vries syndrome see paper … - - Isolated (sporadic) 7y - - - - David Koolen 00117333
0000092552 Koolen-de Vries syndrome see paper … - - Isolated (sporadic) 8y11m - - - - David Koolen 00117334
0000092553 Koolen-de Vries syndrome see paper … - - Isolated (sporadic) 10y10m - - - - David Koolen 00117335
0000092554 Koolen-de Vries syndrome see paper … - - Isolated (sporadic) 13y - - - - David Amor 00117336
0000092555 Koolen-de Vries syndrome see paper … - - Isolated (sporadic) 20y3m - - - - David Koolen 00117337
0000092556 Koolen-de Vries syndrome see paper … - - Isolated (sporadic) 46y - - - - David Koolen 00117338
0000092559 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 7m - - - - David Koolen 00043768
0000092560 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 12m - - - - David Koolen 00043769
0000092561 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 1y2m - - - - David Koolen 00043770
0000092562 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 2y7m - - - - David Koolen 00043771
0000092563 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 3y - - - - David Koolen 00043772
0000092564 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 3y6m - - - - David Koolen 00043773
0000092565 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 4y5m - - - - David Koolen 00043774
0000092566 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 5y3m - - - - David Koolen 00043791
0000092567 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 5y6m - - - - David Koolen 00043792
0000092568 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 8y7m - - - - David Koolen 00043793
0000092569 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 9y - - - - David Koolen 00043794
0000092570 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 10y - - - - David Koolen 00043795
0000092571 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 10y2m - - - - David Koolen 00043796
0000092572 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 11y8m - - - - David Koolen 00043797
0000092573 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 12y2m - - - - David Koolen 00043798
0000092574 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 14y - - - - David Koolen 00043799
0000092575 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 16y - - - - David Koolen 00043800
0000092576 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 16y3m - - - - David Koolen 00043801
0000092577 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 20y - - - - David Koolen 00043802
0000092578 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 27y - - - - David Koolen 00043803
0000092579 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 32y11m - - - - David Koolen 00043804
0000092580 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 43y - - - - David Koolen 00043805
0000092581 17q21.31 deletion syndrome, see paper; … - - Isolated (sporadic) 50y1m - - - - David Koolen 00043806
0000233136 Caesarian section; hypotonia; poor sucking; epilepsy; TIA; developmental delay; facial hypotonia; broad nasal tip; prominent nasal bridge; microdontia; clinodactyly of the fifth finger on both hands; hypotonia of the lower limbs; hypermobility and endorotation of her feet. - - Isolated (sporadic) - - - - - Alexander Dingemans 00307401
0000233137 caesarian section; hypotonia; hypoxia; bradycardia; epilepsy; developmental delay; patent ductus arteriousus; scapula alata; pes planus; protruding ears; thin upper lip; upslanted palpebral fissures ; low hanging columella nasi; hypoplastic alae nasi and a wide mouth; cerebellar hypoplasia; friendly nature; cryptorchidism - - Isolated (sporadic) 05y - - - - Alexander Dingemans 00307402
0000233138 plagiocephaly; developmental delay; hypotonia; torticollis; constipation; epilepsy; happy disposition - - Unknown 05y - - - - Alexander Dingemans 00307403
0000233231 see paper; ... - - Isolated (sporadic) 10y - - - - Alexander Dingemans 00307400
0000274645 DD; ID; muscular hypotonia; ptosis; short stature; hyperlaxity (Multiple systems) - Koolen-De Vries syndrome Familial - - - - - LOVD 00380792
0000351790 Hypotonia, Intellectual disability, mild, Seizure, Abnormal brain morphology, Multicystic kidney dysplasia, Aortic regurgitation, Joint hypermobility, Pes valgus, Scoliosis, Bicuspid aortic valve, Mitral valve prolapse, Abnormal ascending aorta morphology, Hypoplasia of the corpus callosum, Strabismus, Astigmatism, Arachnodactyly, Periventricular leukomalacia, Infantile encephalopathy - - Isolated (sporadic) 11y - - - - Andreas Laner 00466425
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