Global Variome shared LOVD
LINC00052 (long intergenic non-protein coding RNA 52)
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Phenotypes for disease #04249 (macular dystrophy (dystrophy, macular))
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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all entries containing 'South Asian', but not containing 'South East Asian'
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565 entries on 6 pages. Showing entries 1 - 100.
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Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000028856
Macular dystrophy
-
-
Familial, autosomal recessive
-
-
25y
decreased visual acuity
-
Frans Cremers
00038313
0000028857
Macular dystrophy
-
-
Familial, autosomal recessive
-
-
32y
decreased visual acuity
-
Frans Cremers
00038314
0000057099
macular dystrophy
-
-
Unknown
-
-
21y
unknown
-
Stéphanie Cornelis
00077324
0000057859
macular dystrophy
-
-
Unknown
-
-
-
unknown
-
Stéphanie Cornelis
00078084
0000057860
macular dystrophy
-
-
Unknown
-
-
-
unknown
-
Stéphanie Cornelis
00078085
0000057861
macular dystrophy
-
-
Unknown
-
-
-
unknown
-
Stéphanie Cornelis
00078086
0000057862
macular dystrophy
-
-
Unknown
-
-
-
unknown
-
Stéphanie Cornelis
00078087
0000057863
macular dystrophy
-
-
Unknown
-
-
-
unknown
-
Stéphanie Cornelis
00078088
0000057864
macular dystrophy
-
-
Unknown
-
-
-
unknown
-
Stéphanie Cornelis
00078089
0000067132
-
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00087599
0000117047
Age diagnosis 32
-
-
Familial, autosomal recessive
-
-
-
-
-
Rob W.J. Collin
00144269
0000117059
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Rob W.J. Collin
00144281
0000272724
bilateral yellowish yolk-like lesions in the macula
-
-
Familial, autosomal dominant
-
-
-
-
-
Ruifang Sui
00377567
0000272725
see paper; ...
North Carolina macular dystrophy
MCDR1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00377571
0000272726
see paper; ...
North Carolina macular dystrophy
MCDR1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00377572
0000272727
see paper; ...
North Carolina macular dystrophy
MCDR1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00377573
0000272728
see paper; ...
North Carolina macular dystrophy
MCDR1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00377574
0000272729
see paper; ...
North Carolina macular dystrophy
MCDR1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00377575
0000272730
see paper; ...
North Carolina macular dystrophy
MCDR1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00377576
0000272731
see paper; ...
North Carolina macular dystrophy
MCDR1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00377577
0000272732
see paper; ...
North Carolina macular dystrophy
MCDR1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00377578
0000272733
see paper; ...
North Carolina macular dystrophy
MCDR1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00377579
0000272734
see paper; ...
North Carolina macular dystrophy
MCDR1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00377580
0000272735
see paper; ...
North Carolina macular dystrophy
MCDR1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00377581
0000272736
see paper; ...
North Carolina macular dystrophy
MCDR1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00377582
0000272738
see paper; ...
progressive bifocal chorioretinal atrophy
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00377584
0000272739
see paper; ...
progressive bifocal chorioretinal atrophy
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00377585
0000272740
see paper; ...
progressive bifocal chorioretinal atrophy
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00377586
0000272741
see paper; ...
-
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00377587
0000273204
HP:0000662, HP:0000613, HP:0001129, HP:0000007, HP:0007754
dystrophy, macular (MCD)
-
Familial, autosomal recessive
-
-
-
-
-
Jinu Han
00378062
0000273414
HP:0000662, HP:0000613, HP:0001129, HP:0003745, HP:0007754, HP:0032037
dystrophy, macular (MCD)
-
Familial, autosomal recessive
-
-
-
-
-
Jinu Han
00379541
0000273498
HP:0030515, HP:0001129, HP:0000551, HP:0003745, HP:0007754
dystrophy, macular (MCD)
-
Familial, autosomal recessive
-
-
-
-
-
Jinu Han
00379654
0000274006
HP:0001141, HP:0000662, HP:0000613, HP:0001123, HP:0000551, HP:0007754
dystrophy, macular (MCD)
-
Familial, autosomal recessive
-
-
-
-
-
Jinu Han
00380151
0000339577
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450522
0000339578
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450523
0000339579
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450524
0000339580
-
cone-rod dystrophy
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450525
0000339581
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450526
0000339582
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450527
0000339583
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450528
0000339584
-
cone-rod dystrophy
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450529
0000339585
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450530
0000339586
-
macular dystrophy-PS
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450531
0000339587
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450532
0000339588
-
macular dystrophy
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450533
0000339589
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450534
0000339590
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450535
0000339591
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450536
0000339592
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450537
0000339593
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450538
0000339594
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450539
0000339595
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450540
0000339596
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450541
0000339597
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450542
0000339598
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450543
0000339599
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450544
0000339600
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450545
0000339601
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450546
0000339602
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450547
0000339603
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450548
0000339604
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450549
0000339605
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450550
0000339606
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450551
0000339607
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450552
0000339608
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450553
0000339609
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450554
0000339610
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450555
0000339611
-
cone-rod dystrophy
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450556
0000339612
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450557
0000339613
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450558
0000339614
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450559
0000339615
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450560
0000339616
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450561
0000339617
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450562
0000339618
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450563
0000339619
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450564
0000339620
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450565
0000339621
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450566
0000339622
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450567
0000339623
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450568
0000339624
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450569
0000339625
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450570
0000339626
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450571
0000339627
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450572
0000339628
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450573
0000339629
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450574
0000339630
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450575
0000339631
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450576
0000339632
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450577
0000339633
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450578
0000339634
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450579
0000339635
-
retinitis pigmentosa
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450580
0000339636
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450581
0000339637
-
macular dystrophy-I
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450582
0000339638
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450583
0000339639
-
cone-rod dystrophy
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450584
0000339640
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450585
0000339641
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450586
0000339642
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450587
0000339643
-
Stargardt disease
-
Unknown
-
-
-
-
-
Rebekkah Hitti-Malin
00450588
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