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Phenotypes for disease #01372 (WGVRP (Wagner syndrome), OMIM:143200)
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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Column type
Example
Matches
Text
Arg
all entries containing 'Arg'
space
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|
Text
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!
Text
!fs
all entries not containing 'fs'
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Text
^p.(Arg
all entries beginning with 'p.(Arg'
$
Text
Ser)$
all entries ending with 'Ser)'
=""
Text
=""
all entries with this field empty
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Text
="p.0"
all entries exactly matching 'p.0'
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all entries with this field not empty
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Text
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combination
Text
*|Ter !fs
all entries containing '*' or 'Ter' but not containing 'fs'
Date
2020
all entries matching the year 2020
|
Date
2020-03|2020-04
all entries matching March or April, 2020
!
Date
!2020-03
all entries not matching March, 2020
<
Date
<2020
all entries before the year 2020
<=
Date
<=2020-06
all entries in or before June, 2020
>
Date
>2020-06
all entries after June, 2020
>=
Date
>=2020-06-15
all entries on or after June 15th, 2020
combination
Date
2019|2020 <2020-03
all entries in 2019 or 2020, and before March, 2020
Numeric
23
all entries exactly matching 23
|
Numeric
23|24
all entries exactly matching 23 or 24
!
Numeric
!23
all entries not exactly matching 23
<
Numeric
<23
all entries lower than 23
<=
Numeric
<=23
all entries lower than, or equal to, 23
>
Numeric
>23
all entries higher than 23
>=
Numeric
>=23
all entries higher than, or equal to, 23
combination
Numeric
>=20 <30 !23
all entries with values from 20 to 29, but not equal to 23
Some more advanced examples:
Example
Matches
Asian
all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
Asian !Caucasian
all entries containing 'Asian' but not containing 'Caucasian'
Asian|African !Caucasian
all entries containing 'Asian' or 'African', but not containing 'Caucasian'
"South Asian"
all entries containing 'South Asian', but not containing 'South East Asian'
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20 entries on 1 page. Showing entries 1 - 20.
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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
0000061381
-
-
-
Unknown
-
-
-
-
-
Burin des Roziers Cyril
00079999
0000061382
-
-
-
Unknown
-
-
-
-
-
Burin des Roziers Cyril
00080000
0000061383
see paper; ..., ocular phenotypes includes empty vitreous with fibrillary condensations, avascular membrane, perivascular sheathing, progressive chorioretinal dystrophy (similar to Wagner syndrome)
-
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00081742
0000061384
see paper; ...
-
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00081743
0000308886
see paper
Wagner disease
WGVRP
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00417399
0000308887
see paper
Wagner disease
WGVRP
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00417400
0000308888
see paper
Wagner disease
WGVRP
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00417401
0000308889
see paper
Wagner disease
WGVRP
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00417402
0000308890
see paper
Wagner disease
WGVRP
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00417403
0000308891
see paper
Wagner disease
WGVRP
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00417404
0000308892
see paper
Wagner disease
WGVRP
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00417405
0000308893
see paper
Wagner disease
WGVRP
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00417406
0000308894
see paper
Wagner disease
WGVRP
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00417407
0000308895
see paper
Wagner disease
WGVRP
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00417408
0000315270
ophtalmological examinations right, left eye (no view of fundus because of opacity of anterior ocular media): best corrected visual acuity: hand movement, 20/25; recent refraction spherical equivalent: -0.875, 0.25; past (presurgical) refraction spherical equivalent: not available, not available; axial length, mm: not available, 23.44; lens status: anterior chamber intraocular lens pupillary membrane, anterior chamber intraocular lens; retinal detachment age, y:not available; surgery: cataract extraction/intraocular lens tube shunt, cataract extraction/intraocular lens; optically empty vitreous: not available, yes; vitreal avascular membranes: not available, yes; retinal traction: not available, none; chorioretinal atrophy: not available, mild; retinal pigmentary changes: not available, mild; ocular alignment: orthophoria, orthophoria; visual field: not available, paracentral scotoma
-
vitreoretinopathy, Wagner (WGVRP, Wagner syndrome)
Familial, autosomal dominant
60y
-
-
-
-
LOVD
00424062
0000315271
ophtalmological examinations right, left eye: best corrected visual acuity: 20/20, 20/25; recent refraction spherical equivalent: -2, -0.25; past (presurgical) refraction spherical equivalent: not available, not available; axial length, mm: 24.69, 24.46; lens status: posterior chamber intraocular lens, posterior chamber intraocular lens; retinal detachment age, y:not available; surgery: cataract extraction/intraocular lens, cataract extraction/intraocular lens; optically empty vitreous: yes, yes; vitreal avascular membranes: yes, yes; retinal traction: moderate, moderate; chorioretinal atrophy: moderate, moderate; retinal pigmentary changes: moderate, moderate; ocular alignment: exotropia, exotropia; visual field: ring scotoma, ring scotoma
-
vitreoretinopathy, Wagner (WGVRP, Wagner syndrome)
Familial, autosomal dominant
37y
-
-
-
-
LOVD
00424063
0000315272
ophtalmological examinations right, left eye (no view of fundus because of opacity of anterior ocular media): best corrected visual acuity: no light perception, 20/400; recent refraction spherical equivalent: not available, Plano; past (presurgical) refraction spherical equivalent: not available, not available; axial length, mm: not available, 22.38; lens status: Dense nuclear sclerotic cataract, posterior chamber intraocular lens; retinal detachment age, y:5; surgery: scleral buckle/pars plana vitrectomy, none; optically empty vitreous: not available, yes; vitreal avascular membranes: not available, yes; retinal traction: not available, mild; chorioretinal atrophy: not available, severe; retinal pigmentary changes: not available, severe; ocular alignment: exotropia, exotropia; visual field: not available, severe constriction
-
vitreoretinopathy, Wagner (WGVRP, Wagner syndrome)
Familial, autosomal dominant
40y
-
-
-
-
LOVD
00424064
0000315273
ophtalmological examinations right, left eye: best corrected visual acuity: 20/20, 20/32; recent refraction spherical equivalent: not available, -1; past (presurgical) refraction spherical equivalent: (age 14 y) -1.00 + 1.00 x 90, (age 14 y) -1.00 + 2.00 x 90; axial length, mm: 24.56, 25.07; lens status: Clear, Clear; retinal detachment age, y:not available; surgery: none, scleral buckle/pars plana vitrectomy; optically empty vitreous: yes, yes; vitreal avascular membranes: yes, yes; retinal traction: severe, severe; chorioretinal atrophy: none, none; retinal pigmentary changes: none, none; ocular alignment: orthophoria, orthophoria; visual field: enlarged blind spot, paracentral scotoma
-
vitreoretinopathy, Wagner (WGVRP, Wagner syndrome)
Familial, autosomal dominant
16y
-
-
-
-
LOVD
00424065
0000315274
ophtalmological examinations right, left eye (no view of fundus because of opacity of anterior ocular media): best corrected visual acuity: no light perception, 20/160; recent refraction spherical equivalent: not available, -0.25; past (presurgical) refraction spherical equivalent: (age 4 y) +2.50 sph, (age 4 y) +2.50 sph; axial length, mm: not available, 22.18; lens status: Dense nuclear sclerotic cataract, Clear; retinal detachment age, y:9; surgery: scleral buckle/pars plana vitrectomy, none; optically empty vitreous: not available, yes; vitreal avascular membranes: not available, yes; retinal traction: not available, moderate; chorioretinal atrophy: not available, severe; retinal pigmentary changes: not available, severe; ocular alignment: orthophoria, orthophoria; visual field: not available, moderate constriction
-
vitreoretinopathy, Wagner (WGVRP, Wagner syndrome)
Familial, autosomal dominant
16y
-
-
-
-
LOVD
00424066
0000315275
ophtalmological examinations right, left eye: best corrected visual acuity: 20/200, 20/50; recent refraction spherical equivalent: -3.25, 0.75; past (presurgical) refraction spherical equivalent: (age 2.5 y) 1.25 + 3.00 x 90, (age 2.5 y) -1.50+ 4.25 x 95; axial length, mm: 23.62, 22.85; lens status: posterior subcapsular cataract, Clear; retinal detachment age, y:8; surgery: scleral buckle/pars plana vitrectomy, none; optically empty vitreous: not availabled, yes; vitreal avascular membranes: not availabled, yes; retinal traction: none, none; chorioretinal atrophy: moderate, moderate; retinal pigmentary changes: none, none; ocular alignment: exotropia, exotropia; visual field: nasal scotoma, superior scotoma
-
vitreoretinopathy, Wagner (WGVRP, Wagner syndrome)
Familial, autosomal dominant
11y
-
-
-
-
LOVD
00424067
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