Global Variome shared LOVD
GABRD (gamma-aminobutyric acid (GABA) A receptor, d...)
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Global Variome, with Curator vacancy
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Phenotypes for disease #01814 (GLC3A (glaucoma, congenital, primary, type 3A (GLC-3A)), OMIM:231300)
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
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Date
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Date
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Date
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Date
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Date
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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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Numeric
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all entries with values from 20 to 29, but not equal to 23
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all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
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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
0000038632
early onset (0–3y) aggressive glaucoma, increased IOP, corneal edema, excessive tearing, photophobia, buphthalmos, cloudy cornea
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00051844
0000038633
early onset (0–3y) aggressive glaucoma, increased IOP, corneal edema, excessive tearing, photophobia, buphthalmos, cloudy cornea
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00051846
0000038634
early onset (0–3y) aggressive glaucoma, increased IOP, corneal edema, excessive tearing, photophobia, buphthalmos, cloudy cornea
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00051841
0000038635
early onset (0–3y) aggressive glaucoma, increased IOP, corneal edema, excessive tearing, photophobia, buphthalmos, cloudy cornea
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00051871
0000038636
early onset (0–3y) aggressive glaucoma, increased IOP, corneal edema, excessive tearing, photophobia, buphthalmos, cloudy cornea
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00051843
0000038637
early onset (0–3y) aggressive glaucoma, increased IOP, corneal edema, excessive tearing, photophobia, buphthalmos, cloudy cornea
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00051837
0000038638
early onset (0–3y) aggressive glaucoma, increased IOP, corneal edema, excessive tearing, photophobia, buphthalmos, cloudy cornea
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00051875
0000038639
early onset (0–3y) aggressive glaucoma, increased IOP, corneal edema, excessive tearing, photophobia, buphthalmos, cloudy cornea
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00051842
0000038640
early onset (0–3y) aggressive glaucoma, increased IOP, corneal edema, excessive tearing, photophobia, buphthalmos, cloudy cornea
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00051838
0000038641
early onset (0–3y) aggressive glaucoma, increased IOP, corneal edema, excessive tearing, photophobia, buphthalmos, cloudy cornea
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00051839
0000061317
increased intraocular pressure (HP:0007906) OD/OS 52/44, cup to disc ratio no view/no view, visual acuity no light perception/light perception, increased corneal diameter (HP:0000485), corneal edema (HP:0012040), corneal haze, spheroidal degeneration (HP:0007705)
-
-
Familial, autosomal recessive
45y
-
-
-
-
Johan den Dunnen
00081683
0000061318
increased intraocular pressure (HP:0007906) OD/OS 16/16; cup to disc ratio 0.6/0.4; visual acuity light perception/light perception; increased corneal diameter (HP:0000485); bilateral buphthalmos (HP:0000557); bilateral myopic fundus
-
-
Familial, autosomal recessive
4y
-
-
-
-
Johan den Dunnen
00081684
0000061319
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00081685
0000061320
increased intraocular pressure (HP:0007906) OD/OS 40/32; cup to disc ratio 0.7/0.4; visual acuity light perception/hand movement; increased corneal diameter (HP:0000485); bilateral buphthalmos (HP:0000557); corneal opacity (HP:0007957)
-
-
Familial, autosomal recessive
2y
-
-
-
-
Johan den Dunnen
00081686
0000061321
increased intraocular pressure (HP:0007906) OD/OS 26/20; cup to disc ratio no view/no view; visual acuity hand movement/hand movement; corneal diameter lateral >14mm; bilateral corneal opacity (HP:0007957); vascularization
-
-
Familial, autosomal recessive
12y
-
-
-
-
Johan den Dunnen
00081687
0000061322
visual acuity light perception/light perception; ; corneal opacity (HP:0007957)
-
-
Familial, autosomal recessive
14y
-
-
-
-
Johan den Dunnen
00081688
0000061323
increased intraocular pressure (HP:0007906) OD/OS 44/30; cup to disc ratio 0.8/no view; visual acuity light perception/light perception; increased corneal diameter (HP:0000485); bilateral buphthalmos (HP:0000557); bilateral megalocornea (HP:0000485)
-
-
Familial, autosomal recessive
2y
-
-
-
-
Johan den Dunnen
00081689
0000061324
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00081690
0000061325
increased intraocular pressure (HP:0007906) OD/OS 30/26; cup to disc ratio 0.8/0.6; visual acuity light perception/light perception; increased corneal diameter (HP:0000485); bilateral buphthalmos (HP:0000557); bilateral corneal opacity (HP:0007957)
-
-
Familial, autosomal recessive
2y
-
-
-
-
Johan den Dunnen
00081691
0000061326
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00081692
0000061327
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00081693
0000061328
increased intraocular pressure (HP:0007906) OD/OS ?/38; visual acuity light perception/light perception; increased corneal diameter (HP:0000485); bilateral buphthalmos (HP:0000557); megalocornea (HP:0000485)
-
-
Familial, autosomal recessive
3y
-
-
-
-
Johan den Dunnen
00081694
0000061329
increased intraocular pressure (HP:0007906) OD/OS 22/20; cup to disc ratio no view/no view; visual acuity light perception/light perception; corneal diameter 13.0/14.0; bilateral buphthalmos (HP:0000557); bilateral corneal opacity (HP:0007957)
-
-
Familial, autosomal recessive
3y
-
-
-
-
Johan den Dunnen
00081695
0000061330
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00081696
0000061331
increased intraocular pressure (HP:0007906) OD/OS 28/28; cup to disc ratio 1.0/1.0; visual acuity /36/4/12; increased corneal diameter (HP:0000485); bilateral buphthalmos (HP:0000557); bilateral megalocornea (HP:0000485)
-
-
Familial, autosomal recessive
10y
-
-
-
-
Johan den Dunnen
00081697
0000061332
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00081698
0000061333
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00081699
0000061334
increased intraocular pressure (HP:0007906) OD/OS 19/22; cup to disc ratio 0.9/0.9; visual acuity counting fingers/counting fingers; increased corneal diameter (HP:0000485); bilateral buphthalmos (HP:0000557)
-
-
Familial, autosomal recessive
13y
-
-
-
-
Johan den Dunnen
00081700
0000061335
increased intraocular pressure (HP:0007906) OD/OS 38/?; cup to disc ratio no view/no view; visual acuity hand movement/no light perception; increased corneal diameter (HP:0000485); right buphthalmos (HP:0000557); left phthisical eye
-
-
Familial, autosomal recessive
14y
-
-
-
-
Johan den Dunnen
00081701
0000061336
increased intraocular pressure (HP:0007906) OD/OS 53/?; cup to disc ratio 0.7/no view; visual acuity hand 6/60/no light perception; increased corneal diameter (HP:0000485); right megalocornea (HP:0000485); right corneal haze
-
-
Familial, autosomal recessive
12y
-
-
-
-
Johan den Dunnen
00081702
0000061337
visual acuity light perception/light perception; buphthalmos (HP:0000557); corneal opacity (HP:0007957)
-
-
Familial, autosomal recessive
12y
-
-
-
-
Johan den Dunnen
00081703
0000061338
visual acuity no light perception/no light perception; corneal opacity (HP:0007957)
-
-
Familial, autosomal recessive
10y
-
-
-
-
Johan den Dunnen
00081704
0000061339
buphthalmos (HP:0000557); corneal opacity (HP:0007957)
-
-
Familial, autosomal recessive
4y
-
-
-
-
Johan den Dunnen
00081705
0000275937
anterior segment developmental anomalies including glaucoma; MIM, 231300 or 617315
MIM, 231300 or 617315
-
Familial, autosomal recessive
-
-
-
-
-
LOVD
00382095
0000275938
anterior segment developmental anomalies including glaucoma; MIM, 231300 or 617315
MIM, 231300 or 617315
-
Familial, autosomal recessive
-
-
-
-
-
LOVD
00382096
0000275939
anterior segment developmental anomalies including glaucoma; MIM, 231300 or 617315
MIM, 231300 or 617315
-
Familial, autosomal recessive
-
-
-
-
-
LOVD
00382097
0000275940
anterior segment developmental anomalies including glaucoma; MIM, 231300 or 617315
MIM, 231300 or 617315
-
Familial, autosomal recessive
-
-
-
-
-
LOVD
00382098
0000275941
anterior segment developmental anomalies including glaucoma; MIM, 231300 or 617315
MIM, 231300 or 617315
-
Familial, autosomal recessive
-
-
-
-
-
LOVD
00382099
0000275942
anterior segment developmental anomalies including glaucoma; MIM, 231300 or 617315
MIM, 231300 or 617315
-
Familial, autosomal recessive
-
-
-
-
-
LOVD
00382100
0000275943
anterior segment developmental anomalies including glaucoma; MIM, 231300 or 617315
MIM, 231300 or 617315
-
Familial, autosomal recessive
-
-
-
-
-
LOVD
00382101
0000275944
anterior segment developmental anomalies including glaucoma; MIM, 231300 or 617315
MIM, 231300 or 617315
-
Familial, autosomal recessive
-
-
-
-
-
LOVD
00382102
0000275945
anterior segment developmental anomalies including glaucoma; MIM, 231300 or 617315
MIM, 231300 or 617315
-
Familial, autosomal recessive
-
-
-
-
-
LOVD
00382103
0000275946
anterior segment developmental anomalies including glaucoma; MIM, 231300 or 617315
MIM, 231300 or 617315
-
Familial, autosomal recessive
-
-
-
-
-
LOVD
00382104
0000275960
anterior segment developmental anomalies including glaucoma; MIM, 225750
MIM, 225750
-
Familial, autosomal recessive
-
-
-
-
-
LOVD
00382118
0000275963
anterior segment developmental anomalies including glaucoma; MIM, 217700 or 217400
MIM, 217700 or 217400
-
Familial, autosomal recessive
-
-
-
-
-
LOVD
00382121
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