Phenotypes for disease #05412 (maculopathy (maculopathy))

16 entries on 1 page. Showing entries 1 - 16.
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0000127818 Maculopathy - - Familial, autosomal recessive - - - - - Dror Sharon 00155318
0000127831 Maculopathy - - Familial, autosomal recessive - - - - - Dror Sharon 00155331
0000127833 Maculopathy - - Familial, autosomal recessive - - - - - Dror Sharon 00155333
0000127837 Maculopathy - - Familial, autosomal recessive - - - - - Dror Sharon 00155337
0000127839 Maculopathy - - Familial, autosomal recessive - - - - - Dror Sharon 00155339
0000127845 Maculopathy - - Familial, autosomal recessive - - - - - Dror Sharon 00155345
0000127856 Maculopathy - - Familial, autosomal recessive - - - - - Dror Sharon 00155356
0000127864 Maculopathy - - Familial, autosomal recessive - - - - - Dror Sharon 00155364
0000201911 - - Large population study of Age-related Macular Degeneration (AMD) in UK. Unknown - - - - - Christian Drouet 00264064
0000203540 - - Patients presenting with age-related macular degeneration Unknown - - - - - Christian Drouet 00265753
0000245500 Bilateral, Symmetrical, Cuticular Drusen - Fundus: Multiple large, confluent drusen in the central macula and nasal retina Ocular Coherence Tomography (OCT): Numerous confluent drusen in the macula Vision at time of examination was unaffected. Familial, autosomal recessive 42y - - - - Lance P Doucette 00327053
0000245691 - - Fundus/History: Bilateral macular schisis, vitreous veils, mild pigmentary retinopathy. Right eye developed shallow rhegmatogenous inferior retinal detachment, and was treated by scleral buckle procedure, cryotherapy with gas injection. Ocular Coherence Tomography: Bilateral parafoveal thinning of the outer retina layers. Central splitting between the inner nuclear and the outer plexiform layer. Electroretinogram (ERG): Small residual cone flicker (6.2 microV in OD, and 7.1 microV in OS) with no measurable responses to ISCE standard seriesd ERG in ffERG Familial, autosomal recessive 11y - - - - Lance P Doucette 00327400
0000245750 - - Fundus: No specific findings OCT: Normal ERG:Central loss on multi-focal electroretinogram (abnormal ERG HP:0000512) - Reduced Visual Acuity 20/40 OU (HP:0007663) Familial, autosomal recessive 15y - - - - Lance P Doucette 00327461
0000245752 Retinopathy - Fundus findings: Circumscribed central retinal atrophy (Retinal atrophy HP:0001105) Ocular coherence tomography (OCT): Atrophy of outer retina. Bruch's membrane is absent in the central fovea. Electroretinogram: Normal ffERG in the right eye; reduced cone flash and flicker in the left eye (Abnormal ERG HP:0000512) Familial, autosomal recessive 29y - - - - Lance P Doucette 00327463
0000300515 - - - Familial, autosomal dominant - - - - - Oscar F Chacon-Camacho 00408394
0000308985 maculopathy - see paper Isolated (sporadic) - - - - - Johan den Dunnen 00417503
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