Global Variome shared LOVD
E2F3 (E2F transcription factor 3)
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Phenotypes for disease #01006 (KDVS (Koolen-De Vries syndrome (KDVS, 17q21.31 deletion syndrome)), OMIM:610443)
Legend
Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
Diagnosis/Initial
: initial diagnosis, before molecular testing
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
Inheritance
: Indicates the inheritance of the phenotype in the family; unknown, familial (autosomal/X-linked, dominant/ recessive), paternal (Y-linked), maternal (mitochondrial), isolated (sporadic) or complex
All options:
Unknown
Familial
Familial, autosomal dominant
Familial, autosomal recessive
Familial, X-linked
Familial, X-linked dominant
Familial, X-linked dominant, male sparing
Familial, X-linked recessive
Paternal, Y-linked
Maternal, mitochondrial
Isolated (sporadic)
Di-genic
Complex
- = Not applicable
Age/Examination
: age at which the individual was examined.
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Age/Diagnosis
: age diagnosis was confirmed
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Age/Onset
: Age first symptoms disease appeared in individual:
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Phenotype/Onset
: individual's phenotype at Age/Onset described using HPO
Protein
: result from protein staining
How to query this table
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all entries beginning with 'p.(Arg'
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Date
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all entries matching the year 2020
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Date
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all entries matching March or April, 2020
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Date
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all entries not matching March, 2020
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Date
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all entries before the year 2020
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Date
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Date
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all entries after June, 2020
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Date
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all entries on or after June 15th, 2020
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Date
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all entries in 2019 or 2020, and before March, 2020
Numeric
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all entries exactly matching 23
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Numeric
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all entries exactly matching 23 or 24
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Numeric
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all entries not exactly matching 23
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Numeric
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all entries lower than 23
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Numeric
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all entries lower than, or equal to, 23
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Numeric
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all entries higher than 23
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Numeric
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Numeric
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all entries with values from 20 to 29, but not equal to 23
Some more advanced examples:
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all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
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all entries containing 'South Asian', but not containing 'South East Asian'
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45 entries on 1 page. Showing entries 1 - 45.
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How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
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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