Global Variome shared LOVD
P2RY13 (purinergic receptor P2Y, G-protein coupled, 13)
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Phenotypes for disease #01178 (AN (aniridia (AN)))
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
2020
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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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 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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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, or equal to, 23
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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 'Asian' but not containing 'Caucasian'
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42 entries on 1 page. Showing entries 1 - 42.
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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
0000034728
-
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00047290
0000051156
lens opacity, aniridia, corneal limbal insufficiency, nystagmus, severe axile myopia, posterior capsular reaction after lens surgery
-
-
Unknown
-
-
-
-
-
Deepti Anand
00065003
0000060495
Aniridia (OMIM:106210)
-
-
Isolated (sporadic)
-
-
-
-
-
Daniel Trujillano
00080926
0000156533
aniridia
aniridia
-
Unknown
-
-
-
-
-
Andreas Laner
00036451
0000156536
aniridia
aniridia
-
Unknown
-
-
-
-
-
Andreas Laner
00036457
0000185979
best corrected visual acuity R/L 0.05/0.02; aniridia-related keratopathy; complete aniridia; cataract; no glauvoma; macular hypoplasia; nystagmus; esotropia; no ptosis; normal psychomotor development
congenital aniridia
AN-1
Familial, autosomal dominant
64y
-
-
-
-
Johan den Dunnen
00246127
0000185980
best corrected visual acuity R/L 0.02/0.02; no aniridia-related keratopathy; complete aniridia; cataract; no glauvoma; macular hypoplasia; nystagmus; no strabismus ; no ptosis; normal psychomotor development
congenital aniridia
AN-1
Familial, autosomal dominant
37y
-
-
-
-
Johan den Dunnen
00246128
0000185981
best corrected visual acuity R/L 0.1/0.1; no aniridia-related keratopathy; complete aniridia; aphakia, posterior capsule opacification; no glauvoma; macular hypoplasia uncertain (because of PCO); nystagmus; no strabismus ; no ptosis; normal psychomotor development
congenital aniridia
AN-1
Familial, autosomal dominant
35y
-
-
-
-
Johan den Dunnen
00246129
0000185982
best corrected visual acuity R/L 0.2/0.2; no aniridia-related keratopathy; complete aniridia; aphakia, posterior capsule opacification; no glauvoma; macular hypoplasia uncertain (because of PCO); nystagmus; exotropia; ptosis; normal psychomotor development
congenital aniridia
AN-1
Familial, autosomal dominant
12y
-
-
-
-
Johan den Dunnen
00246130
0000253925
HP:0000526; HP:0000482; HP:0000568
-
-
Familial, autosomal dominant
-
-
-
-
-
Sarah Seese
00336029
0000272158
bilateral microphthalmia, microcornea, aniridia, ectopia lentis
-
-
Unknown
25y
-
-
-
-
Johan den Dunnen
00376964
0000278020
-
Aniridia
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00384235
0000278030
-
Aniridia
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00384245
0000278076
-
Aniridia
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00384291
0000278123
-
Aniridia
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00384338
0000278203
-
Aniridia
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00384418
0000278213
-
Aniridia
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00384428
0000278292
-
Aniridia
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00384507
0000339471
bilateral aniridia, nystagmus, glaucoma
aniridia
AN1
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00450410
0000339472
bilateral aniridia, glaucoma, cataracts in young adulthood
aniridia
AN1
Unknown
-
-
-
-
-
Johan den Dunnen
00450411
0000339473
aniridia
aniridia
AN1
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00450412
0000339474
bilateral aniridia, cataracts (posterior subcapsular), absent foveal reflexes, no nystagmus, vision right 6/12 N5 and left 6/36 N5, corneas clear with fine limbal vessels peripherally
aniridia
AN1
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00450413
0000339475
bilateral partial aniridia
aniridia
AN1
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00450414
0000339476
variant aniridia: inferior iris defects, peripheral corneal vascularisation, inferior lens opacities, foveal hypoplasia, nystagmus, poor vision
aniridia
AN1
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00450415
0000339477
bilateral aniridia, relatively well-preserved foveas, vision 0.4 logMAR, mild keratopathy as teenager, mild cataracts
aniridia
AN1
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00450416
0000339478
aniridia
aniridia
AN1
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00450417
0000339479
aniridia, type 2 diabetes
aniridia
AN1
Familial
-
-
-
-
-
Johan den Dunnen
00450418
0000339480
aniridia
aniridia
AN1
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00450419
0000339481
aniridia spectrum, iris and foveal hypoplasia, congenital corneal opacification with small lenses apposed to posterior surface of cornea
aniridia
AN1
Familial
-
-
-
-
-
Johan den Dunnen
00450420
0000339482
aniridia; half-sibling both affected
aniridia
AN1
Familial
-
-
-
-
-
Johan den Dunnen
00450421
0000339483
partial aniridia, cataracts (surgery in late 20s)
aniridia
AN1
Familial
-
-
-
-
-
Johan den Dunnen
00450422
0000339484
aniridia
aniridia
AN1
Familial
-
-
-
-
-
Johan den Dunnen
00450423
0000339485
aniridia, glaucoma
aniridia
AN1
Unknown
-
-
-
-
-
Johan den Dunnen
00450424
0000339486
bilateral aniridia
aniridia
AN1
Unknown
-
-
-
-
-
Johan den Dunnen
00450425
0000339487
bilateral aniridia, cataract, drusen at macula and nasal to the optic disc
aniridia
AN1
Unknown
-
-
-
-
-
Johan den Dunnen
00450426
0000339488
bilateral aniridia, congenital cataracts
aniridia
AN1
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00450427
0000339489
bilateral aniridia, cataract (extraction both eyes as teenager)
aniridia
AN1
Unknown
-
-
-
-
-
Johan den Dunnen
00450428
0000339490
sporadic aniridia
aniridia
-
Unknown
-
-
-
-
-
Johan den Dunnen
00450429
0000339491
aniridia presenting as congenital glaucoma, biscuspid aortic valve, mild aortic stenosis
aniridia
-
Unknown
-
-
-
-
-
Johan den Dunnen
00450430
0000339492
bilateral aniridia, glaucoma, opaque right cornea, aortic stenosis requiring neonatal surgery (not dysmorphic)
aniridia
-
Unknown
-
-
-
-
-
Johan den Dunnen
00450431
0000339493
aniridia
aniridia
AN1
Unknown
-
-
-
-
-
Johan den Dunnen
00450432
0000339494
aniridia
aniridia
-
Unknown
-
-
-
-
-
Johan den Dunnen
00450433
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