Phenotypes for disease #04210 (LCA (Leber congenital amaurosis (LCA)))

1109 entries on 12 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     
0000026468 - - - Unknown - - - - - Johan den Dunnen 00033039
0000026472 autosomal recessive retinitis pigmentosa (ARRP) - - Unknown - - - - - Johan den Dunnen 00033043
0000026473 autosomal recessive retinitis pigmentosa (ARRP) - - Unknown - - - - - Johan den Dunnen 00033044
0000026482 - - - Unknown - - - - - Johan den Dunnen 00033053
0000026483 - - - Unknown - - - - - Johan den Dunnen 00033054
0000026485 - - - Unknown - - - - - Johan den Dunnen 00033056
0000026487 - - - Unknown - - - - - Johan den Dunnen 00033058
0000026488 - - - Unknown - - - - - Johan den Dunnen 00033059
0000026489 - - - Unknown - - - - - Johan den Dunnen 00033060
0000026490 - - - Unknown - - - - - Johan den Dunnen 00033061
0000026491 - - - Unknown - - - - - Johan den Dunnen 00033062
0000026493 - - - Unknown - - - - - Johan den Dunnen 00033064
0000026494 - - - Unknown - - - - - Johan den Dunnen 00033065
0000026495 - - - Unknown - - - - - Johan den Dunnen 00033066
0000026497 - - - Unknown - - - - - Johan den Dunnen 00033068
0000026505 - - - Unknown - - - - - Johan den Dunnen 00033076
0000026508 - - - Unknown - - - - - Johan den Dunnen 00033079
0000026509 - - - Unknown - - - - - Johan den Dunnen 00033080
0000026511 - - - Unknown - - - - - Johan den Dunnen 00033082
0000026512 - - - Unknown - - - - - Johan den Dunnen 00033083
0000026513 - - - Unknown - - - - - Johan den Dunnen 00033084
0000026514 - - - Unknown - - - - - Johan den Dunnen 00033085
0000026781 - - - Familial, autosomal recessive - - - - - Leen Abu Safieh 00033352
0000026785 - - - Familial, autosomal recessive - - - - - Leen Abu Safieh 00033356
0000026786 - - - Familial, autosomal recessive - - - - - Leen Abu Safieh 00033357
0000026791 gliosis - - Familial, autosomal recessive - - - - - Leen Abu Safieh 00033362
0000026792 - - - Familial, autosomal recessive - - - - - Leen Abu Safieh 00033363
0000026793 - - - Familial, autosomal recessive - - - - - Leen Abu Safieh 00033364
0000026810 Bilateral contaract; keratoconus;  Oculodigital Phenomena; Onset Visual loss, Nyctalopia - - Familial, autosomal recessive - - - - - Raheel Qamar 00033381
0000026811 Bilateral plasties; Oculodigital Phenomena; Onset Visual loss - - Familial, autosomal recessive - - - - - Raheel Qamar 00033382
0000026812 foveal depression; Onset Visual disturbance, nystagmus - - Familial, autosomal recessive 1y - - - - Raheel Qamar 00033383
0000026813 foveal depression; Onset Visual disturbance, nystagmus - - Familial, autosomal recessive 5y - - - - Raheel Qamar 00033384
0000026815 Pseudophakic; keratoconus; patches of periphral chorio retinal atrophy; Oculodigital Phenomena; Onset Visual loss, Nyctalopia;Photosensitivity - - Familial, autosomal recessive - - - - - Raheel Qamar 00033386
0000026817 Bilateral pigmentary degeneration; significant hyperopia with astigmatism.; Onset Roving nystagmus;sluggish pupils, andphotophobi - - Familial, autosomal recessive 2y - - - - Raheel Qamar 00033388
0000026818 Bluntedfoveal reflex; minimally attenuatedretinal vessels; andmildpigment dispersion with traces of finemottling; Onset Nystagmus, sluggish pupillary responses andmildhyperopiawith astigmatism - - Familial, autosomal recessive 8m - - - - Raheel Qamar 00033389
0000026825 Nystagmus; Onset Severe visual loss - - Familial, autosomal recessive - - - - - Raheel Qamar 00033396
0000026826 Nystagmus; Onset Severe visual loss - - Familial, autosomal recessive - - - - - Raheel Qamar 00033397
0000026834 Nystagmus; mildmottling of maculopathy; high myopia ; Onset Nystagmus - - Familial, autosomal recessive 2y - - - - Raheel Qamar 00033405
0000026835 - - - Familial, autosomal recessive - - - - - Raheel Qamar 00033406
0000026836 foveal depression; Onset Visual disturbance, nystagmus - - Familial, autosomal recessive 3y - - - - Raheel Qamar 00033407
0000026837 - - - Familial, autosomal recessive - - - - - Raheel Qamar 00033408
0000026838 Keratoconus; cataract; foveal depression; Onset Visual disturbance, nystagmus - - Familial, autosomal recessive 23y - - - - Raheel Qamar 00033409
0000026839 foveal depression; Onset Visual disturbance, nystagmus - - Familial, autosomal recessive 27y - - - - Raheel Qamar 00033410
0000026841 Retinal drunes like depositions;  Oculodigital Phenomena; Onset Visual loss, Nyctalopia - - Familial, autosomal recessive - - - - - Raheel Qamar 00033412
0000026842 MildMaculopathy ; Onset Severe pigmentary retinopathy - - Familial, autosomal recessive 24y - - - - Raheel Qamar 00033413
0000026843 - - - Familial, autosomal recessive - - - - - Raheel Qamar 00033414
0000026844 - - - Familial, autosomal recessive - - - - - Raheel Qamar 00033415
0000026845 - - - Familial, autosomal recessive - - - - - Raheel Qamar 00033416
0000026846 dilatedretinal vessels; mainly venules; primarily localisedin the posterior pole;photoreceptors are absent; retinal gliosis was present; Headache andpain in eyes; Bilateral Nysgtagmus - - Familial, autosomal recessive 22y - - - - Raheel Qamar 00033417
0000026847 dilatedretinal vessels; mainly venules; primarily localisedin the posterior pole;photoreceptors are absent; retinal gliosis was present; Headache andpain in eyes; Bilateral Nysgtagmus - - Familial, autosomal recessive 4y - - - - Raheel Qamar 00033418
0000026848 Nystagmus; moderate pigmentry retionopathy;maculopathy atrophy;disc pallor drusen; posterior subcapsular cataract; keratoconus; Onset Poor vision;nystagmus - - Familial, autosomal recessive 30y - - - - Raheel Qamar 00033419
0000026849 Nystagmus; moderate pigmentry retionopathy;maculopathy atrophy;disc pallor drusen; posterior subcapsular cataract; keratoconus; Onset Poor vision;nystagmus - - Familial, autosomal recessive 36y - - - - Raheel Qamar 00033420
0000026850 ? - - Familial, autosomal recessive - - - - - Raheel Qamar 00033421
0000026857 Nystagmus;moderate pigmentry retionpathy;maculopathy atrophy; drusen; presence of white retinal dots; posterior subcapsular cataract; moderate myopia; Onset Poor vision, nystagmus - - Familial, autosomal recessive 17y - - - - Raheel Qamar 00033428
0000026858 - - - Familial, autosomal recessive - - - - - Raheel Qamar 00033429
0000026859 - - - Familial, autosomal recessive - - - - - Raheel Qamar 00033430
0000026862 dilatedretinal vessels; mainly venules; primarily localisedin the posterior pole; Headache andpain in eyes; Bilateral Nysgtagmus - - Familial, autosomal recessive 22y - - - - Raheel Qamar 00033433
0000026863 dilatedretinal vessels; mainly venules; primarily localisedin the posterior pole; Headache andpain in eyes; Bilateral Nysgtagmus - - Familial, autosomal recessive 4y - - - - Raheel Qamar 00033434
0000026864 Visual fieldchanges; ERG reduction; Onset Nystagmus, - - Familial, autosomal recessive - - - - - Raheel Qamar 00033435
0000026865 mild maculopathy; absence of pigmentary retinopathy - - Familial, autosomal recessive 4m - - - - Raheel Qamar 00033436
0000026866 ? - - Familial, autosomal recessive - - - - - Raheel Qamar 00033437
0000026869 Pseudophakic; keratoconus; patches of periphral chorio retinal atrophy;  Oculodigital Phenomena; Onset Visual loss, Nyctalopia, Photosensitivity, Atrophy of retinal pigment andchoroid, pigmentary clumping - - Familial, autosomal recessive - - - - - Raheel Qamar 00033440
0000026870 Keratoconus; Bilateral Contaracts; Oculodigital Phenomena; Onset Visual loss, Nyctalopia;Photosensitivity - - Familial, autosomal recessive - - - - - Raheel Qamar 00033441
0000026875 - - - Familial, autosomal recessive - - - - - Raheel Qamar 00033446
0000026876 Severe Maculopathy; Moderate pigmentary retinopathy - - Familial, autosomal recessive 8y - - - - Raheel Qamar 00033447
0000026877 Onset Severe pigmentary Retinopathy - - Familial, autosomal recessive - - - - - Raheel Qamar 00033448
0000026880 Onset Severe pigmentary Retinopathy - - Familial, autosomal recessive - - - - - Raheel Qamar 00033451
0000026889 Nystagmus; moderate hyperopia; Onset Poor vision;nystagmus - - Familial, autosomal recessive 2y - - - - Raheel Qamar 00033460
0000026890 MildMaculopathy; Onset Severe pigmentary retinopathy - - Familial, autosomal recessive 10y - - - - Raheel Qamar 00033461
0000026891 keratoconu; cataracts; pale optic discs;arteriolar attenuation andintraretinal pigment migration; Onset Night blindness - - Familial, autosomal recessive - - - - - Raheel Qamar 00033462
0000026892 keratoconu; cataracts; pale optic discs;arteriolar attenuation andintraretinal pigment migration; Onset Night blindness - - Familial, autosomal recessive - - - - - Raheel Qamar 00033463
0000026893 ? - - Familial, autosomal recessive - - - - - Raheel Qamar 00033464
0000026894 ? - - Familial, autosomal recessive - - - - - Raheel Qamar 00033465
0000026895 ? - - Familial, autosomal recessive - - - - - Raheel Qamar 00033466
0000026896 ? - - Familial, autosomal recessive - - - - - Raheel Qamar 00033467
0000026900 Onset Severe pigmentary retinopathy - - Familial, autosomal recessive - - - - - Raheel Qamar 00033471
0000026901 - - - Familial, autosomal recessive - - - - - Raheel Qamar 00033472
0000026902 - - - Familial, autosomal recessive - - - - - Raheel Qamar 00033473
0000026903 ? - - Familial, autosomal recessive - - - - - Raheel Qamar 00033474
0000026904 ? - - Familial, autosomal recessive - - - - - Raheel Qamar 00033475
0000026905 ? - - Familial, autosomal recessive - - - - - Raheel Qamar 00033476
0000026906 ? - - Familial, autosomal recessive - - - - - Raheel Qamar 00033477
0000026915 MildMaculopathy; Onset Severe pigmentary retinopathy - - Familial, autosomal recessive 16y - - - - Raheel Qamar 00033486
0000026921 ? - - Familial, autosomal recessive - - - - - Raheel Qamar 00033492
0000026922 MildMaculopathy; Onset Severe pigmentary retinopathy - - Familial, autosomal recessive 17y - - - - Raheel Qamar 00033493
0000026923 MildMaculopathy - - Familial, autosomal recessive 19y - - - - Raheel Qamar 00033494
0000026924 Cataract; foveal depression; Onset Visual disturbance, nystagmus - - Familial, autosomal recessive 33y - - - - Raheel Qamar 00033495
0000026925 Foveal depression; RPE pigmentation abnormalities; Onset Visual disturbance, nystagmus - - Familial, autosomal recessive 40y - - - - Raheel Qamar 00033496
0000026927 Bone specule like changes; Bull's eye appearence; Atrophic macular lesions; drusion like deposits;  Oculodigital Phenomena; Onset Visual Loss, Severe pigmentary retinopathy, Atrophy of retinal pigment, mottling of hypopigmentation. - - Familial, autosomal recessive - - - - - Raheel Qamar 00033498
0000026928 Cataract; Melanin abnormalities; foveal depression; Onset Visual disturbance, nystagmus - - Familial, autosomal recessive 40y - - - - Raheel Qamar 00033499
0000026929 RPE pigmentation abnormalities; foveal depression; Onset Visual disturbance, nystagmus - - Familial, autosomal recessive 7y - - - - Raheel Qamar 00033500
0000026930 Melanin abnormalities; foveal depression; Onset Visual disturbance, nystagmus - - Familial, autosomal recessive 39y - - - - Raheel Qamar 00033501
0000026931 Cataract; retinal degeneration; foveal depression; Onset Visual disturbance, nystagmus, visual acuity, nyctalopia - - Familial, autosomal recessive 45y - - - - Raheel Qamar 00033502
0000026946 Severe keratoconus; poor acuity; macular atrophy - - Familial, autosomal recessive - - - - - Raheel Qamar 00033517
0000026947 Severe keratoconus; poor acuity; macular atrophy - - Familial, autosomal recessive - - - - - Raheel Qamar 00033518
0000026948 Severe keratoconus; poor acuity; macular atrophy - - Familial, autosomal recessive - - - - - Raheel Qamar 00033519
0000026949 Grossly intact extraocular movement; sluggishpupillary responses; normal intraocular pressure to palpation;andsevere hyperopia with astigmatism.; Onset Nystagmus - - Familial, autosomal recessive 4m - - - - Raheel Qamar 00033520
0000026950 Nystagmus; Moderate pigmentry retinopathy;bone spicules; mildmolting maculopathy; presence of white retinal dots;myopia; Onset Poor vision, nystagmus - - Familial, autosomal recessive 19y - - - - Raheel Qamar 00033521
0000026951 Nystagmus; Moderate pigmentry retinopathy;bone spicules; maculopathy atrophy; Onset Poor vision, nystagmus - - Familial, autosomal recessive 24y - - - - Raheel Qamar 00033522
0000026952 ? - - Familial, autosomal recessive - - - - - Raheel Qamar 00033523
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