Phenotypes for disease #00116 (ND (Norrie disease), OMIM:310600)

73 entries on 1 page. Showing entries 1 - 73.
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AscendingPhenotype 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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