Phenotypes for disease #04249 (macular dystrophy (dystrophy, macular))

565 entries on 6 pages. Showing entries 1 - 100.
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AscendingPhenotype 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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