Global Variome shared LOVD
HIST1H2BJ (histone cluster 1, H2bj)
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Phenotypes for disease #00116 (ND (Norrie disease), OMIM:310600)
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.
Diagnosis/Initial
: initial diagnosis, before molecular testing
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
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
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
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
Protein
: result from protein staining
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Date
2020
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Date
2020-03|2020-04
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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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combination
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
|
Numeric
23|24
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 higher than, or equal to, 23
combination
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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all entries containing 'South Asian', but not containing 'South East Asian'
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73 entries on 1 page. Showing entries 1 - 73.
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How to query
Phenotype ID
Diagnosis/Initial
Inheritance
Age/Examination
Diagnosis/Definite
Age/Diagnosis
Age/Onset
Phenotype/Onset
Phenotype details
Protein
Owner
Individual ID
0000000085
-
Familial, X-linked recessive
-
-
-
-
-
-
-
Anne Polvi
00000396
0000028048
-
Isolated (sporadic)
-
-
-
-
-
-
-
Frans Cremers
00037527
0000028049
-
Familial
-
-
-
-
-
-
-
Frans Cremers
00037528
0000028050
-
Isolated (sporadic)
-
-
-
-
-
-
-
Frans Cremers
00037529
0000028051
-
Isolated (sporadic)
-
-
-
-
-
-
-
Frans Cremers
00037530
0000028052
-
Isolated (sporadic)
-
-
-
-
-
-
-
Frans Cremers
00037531
0000028053
-
Familial
-
-
-
-
-
-
-
Frans Cremers
00037532
0000028054
-
Familial
-
-
-
-
-
-
-
Frans Cremers
00037533
0000028055
-
Familial
-
-
-
-
-
-
-
Frans Cremers
00037534
0000028057
-
Familial
-
-
-
-
-
-
-
Frans Cremers
00037536
0000028058
-
Isolated (sporadic)
-
-
-
-
-
-
-
Frans Cremers
00037537
0000028059
-
Familial
-
-
-
-
-
-
-
Frans Cremers
00037538
0000028060
-
Familial
-
-
-
-
-
-
-
Frans Cremers
00037539
0000028061
-
Familial
-
-
-
-
-
-
-
Frans Cremers
00037540
0000028062
-
Isolated (sporadic)
-
-
-
-
-
-
-
Frans Cremers
00037541
0000028063
-
Familial
-
-
-
-
-
-
-
Frans Cremers
00037542
0000028064
-
Isolated (sporadic)
-
-
-
-
-
-
-
Frans Cremers
00037543
0000028065
-
Familial
-
-
-
-
-
-
-
Frans Cremers
00037544
0000028066
-
Familial
-
-
-
-
-
-
-
Frans Cremers
00037545
0000028067
-
Isolated (sporadic)
-
-
-
-
-
-
-
Frans Cremers
00037546
0000028068
-
Isolated (sporadic)
-
-
-
-
-
-
-
Frans Cremers
00037547
0000028069
-
Familial
-
-
-
-
-
-
-
Frans Cremers
00037548
0000028071
-
Isolated (sporadic)
-
-
-
-
-
-
-
Frans Cremers
00037550
0000028073
-
Familial
-
-
-
-
-
-
-
Frans Cremers
00037552
0000028074
-
Familial
-
-
-
-
-
-
-
Frans Cremers
00037553
0000028075
-
Isolated (sporadic)
-
-
-
-
-
-
-
Frans Cremers
00037554
0000028076
-
Isolated (sporadic)
-
-
-
-
-
-
-
Frans Cremers
00037555
0000028077
-
Isolated (sporadic)
-
-
-
-
-
-
-
Frans Cremers
00037556
0000028078
-
Isolated (sporadic)
-
-
-
-
-
-
-
Frans Cremers
00037557
0000028079
-
Isolated (sporadic)
-
-
-
-
-
-
-
Frans Cremers
00037558
0000028080
-
Isolated (sporadic)
-
-
-
-
-
-
-
Frans Cremers
00037559
0000028081
-
Familial
-
-
-
-
-
-
-
Frans Cremers
00037560
0000028082
-
Isolated (sporadic)
-
-
-
-
-
-
-
Frans Cremers
00037561
0000028083
-
Familial
-
-
-
-
-
-
-
Frans Cremers
00037562
0000028084
-
Familial
-
-
-
-
-
-
-
Frans Cremers
00037563
0000028085
-
Familial
-
-
-
-
-
-
-
Frans Cremers
00037564
0000028086
-
Unknown
-
-
-
-
-
-
-
Frans Cremers
00037565
0000028087
-
Isolated (sporadic)
-
-
-
-
-
-
-
Frans Cremers
00037566
0000121316
Supranuclear palsy
Unknown
62y
-
-
-
-
-
-
Marc Cruts
00148898
0000121325
Supranuclear palsy
Familial
42y
-
-
-
-
Dementia
-
Marc Cruts
00148907
0000121328
Supranuclear palsy
Familial
42y07m
-
-
-
-
-
-
Marc Cruts
00148910
0000121339
Supranuclear palsy
Familial, autosomal dominant
51y06m
-
-
-
-
-
-
Marc Cruts
00148921
0000121408
Supranuclear palsy
Isolated (sporadic)
40y
-
-
-
-
-
-
Marc Cruts
00148990
0000121445
Supranuclear palsy
Familial
50y
-
-
-
-
-
-
Marc Cruts
00149027
0000121464
Supranuclear palsy
Familial
39y
-
-
-
-
-
-
Marc Cruts
00149046
0000203113
-
Familial, X-linked
00y02m
Norrie-like retinopathy
-
-
leukocoria (HP:0000555)
Norrie's disease (HP:0000407), total retinal detachment (HP:0000541)
-
Jasmine Chen
00265315
0000203149
-
Isolated (sporadic)
00y02m
Norrie-like retinopathy
-
-
leukocoria (HP:0000555)
Norrie disease (HP:0000407), microphthalmia (HP:0000568)
-
Jasmine Chen
00265352
0000203150
-
Familial, X-linked
02y01m
Norrie-like retinopathy
-
-
leukocoria (HP:0000555)
Norrie disease (HP:0000407), total retinal detachment (HP:0000541)
-
Jasmine Chen
00265353
0000203151
-
Isolated (sporadic)
02y00m
Norrie-like retinopathy
-
-
leukocoria (HP:0000555)
Norrie disease (HP:0000407), total retinal detachment (HP:0000541)
-
Jasmine Chen
00265354
0000203152
-
Familial, X-linked
00y06m
Norrie-like retinopathy
-
-
-
Norrie disease (HP:0000407), total retinal detachment
-
Jasmine Chen
00265355
0000209615
Norrie-like retinopathy
Familial, X-linked recessive
19y
Norrie disease
-
-
-
total retinal detachment (HP:0030490)
-
Jasmine Chen
00274677
0000209616
Norrie-like retinopathy
Familial, X-linked recessive
00y06m
Norrie disease
-
-
-
retinal detachment (HP:0030490), vitreoretinal haemorrhage (HP:0007902)
-
Jasmine Chen
00274678
0000210070
Norrie-like retinopathy
Familial, X-linked
01y
Norrie disease
-
00y02m
bilateral leukocoria (HP:0000555)
total retinal detachment (HP:0000541)
-
Jasmine Chen
00275445
0000210072
Norrie-like retinopathy
Familial, X-linked
01y
Norrie disease
-
-
-
-
-
Jasmine Chen
00275447
0000210074
Norrie-like retinopathy
Familial, X-linked
00y04m
Norrie disease
-
-
bilateral leukocoria (HP:0000555)
-
-
Jasmine Chen
00275449
0000210084
Norrie-like retinopathy
Isolated (sporadic)
-
Norrie disease
-
-
-
microphthalmia (HP:0000568), sensorineural hearing loss (HP:0000407), developmental delay (HP:0001249)
-
Jasmine Chen
00275456
0000308396
-
Familial, X-linked recessive
6y
Norrie disease (ND)
3y
-
-
best corrected visual acuity right, left eye:light perception,20/60; initial refractive error:+ 0.75 sphere left eye; slit-lamp examination:normal /normal; fundus: avascular periphery total retinal detachment /avascular periphery, retinal detachment
-
LOVD
00416884
0000308397
-
Familial, X-linked recessive
65y
Norrie disease (ND)
48y
-
-
best corrected visual acuity right, left eye:hand motions,20/40; initial refractive error:-3.75 sphere left eye; slit-lamp examination:white cataract /posterior subcapsular cataract; fundus: congenital retinal fold /temporal dragging of vessels, avascular periphery, retinal detachment
-
LOVD
00416885
0000308398
-
Familial, X-linked recessive
61y
Norrie disease (ND)
57y
-
-
best corrected visual acuity right, left eye:20/25,20/160; initial refractive error:-8.50 sphere right eye; slit-lamp examination:posterior subcapsular cataract /brunescent cataract; fundus: peripheral pigmentary changes /peripheral pigmentary changes
-
LOVD
00416886
0000308399
-
Familial, X-linked recessive
53y
Norrie disease (ND)
6y
-
-
best corrected visual acuity right, left eye:light perception,20/30; initial refractive error:-6.75 sphere right eye/ -8.75 sphere left eye; slit-lamp examination:normal /normal; fundus: congenital retinal fold, retinal detachment /normal
-
LOVD
00416887
0000308400
-
Familial, X-linked recessive
62y
Norrie disease (ND)
47y
-
-
best corrected visual acuity right, left eye:20/50,count fingers; initial refractive error:-2.00 sphere right eye/left eye; slit-lamp examination:normal /posterior subcapsular cataract; fundus: avascular peripheral retina, peripheral fibrotic ridge, temporal dragging of vessels /avascular peripheral retina, peripheral fibrotic ridge, macular dystrophy
-
LOVD
00416888
0000308401
-
Familial, X-linked recessive
53y
Norrie disease (ND)
14y
-
-
best corrected visual acuity right, left eye:enucleation,20/20; initial refractive error:+ 5.00 sphere left eye; slit-lamp examination:enucleation /normal; fundus: retinal detachment /temporal dragging of vessels
-
LOVD
00416889
0000308402
-
Familial, X-linked recessive
33y
Norrie disease (ND)
13y
-
-
best corrected visual acuity right, left eye:20/20,no light perception; initial refractive error:+ 1.00 sphere right eye; slit-lamp examination:normal /white cataract; fundus: temporal dragging of vessels, abnormal vessels /retinal detachment
-
LOVD
00416890
0000308403
-
Familial, X-linked recessive
79y
Norrie disease (ND)
71y
-
-
best corrected visual acuity right, left eye:20/30,20/30; initial refractive error:+ 1.00 sphere right eye/left eye; slit-lamp examination:2 + nuclear sclerosis /2 + nuclear sclerosis; fundus: mild peripheral and central retinal pigment epithelial changes /mild peripheral and central retinal pigment epithelial changes
-
LOVD
00416891
0000308404
-
Familial, X-linked recessive
-
Norrie disease (ND)
-
-
-
-
-
LOVD
00416892
0000308405
-
Familial, X-linked recessive
-
Norrie disease (ND)
-
-
-
moderately affected, FEVR
-
LOVD
00416893
0000308406
-
Familial, X-linked recessive
-
Norrie disease (ND)
-
0m
pseudoglioma
Norrie disease
-
LOVD
00416894
0000308479
-
Familial, X-linked
-
Norrie disease
-
4m
-
no hearing impairment
-
LOVD
00416968
0000308482
-
Familial, X-linked
-
Norrie disease
-
2m
-
no hearing impairment
-
LOVD
00416971
0000308483
-
Familial, X-linked
-
Norrie disease
-
0m
-
hearing impairment
-
LOVD
00416972
0000308484
-
Familial, X-linked
-
Norrie disease
-
0m
-
no hearing impairment
-
LOVD
00416973
0000308485
-
Familial, X-linked
-
Norrie disease
-
1m
-
no hearing impairment
-
LOVD
00416974
0000308881
-
Isolated (sporadic)
-
Norrie disease/bilateral persistent fetal vasculature syndrome
-
-
-
-
-
LOVD
00417394
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