| Disease Browser
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Parent Node:
 Eye Diseases (D005128) |
..Starting node
.. Retinal Diseases (D012164)
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Child Nodes:
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| ........Al Gazali Sabrinathan Nair syndrome (C535617) |
| ........Angioid Streaks (D000793) |
| ........Ausems Wittebol-Post Hennekam syndrome (C538272) |
| ........Bestrophinopathy (C567518) |
| ........BESTROPHINOPATHY, AUTOSOMAL RECESSIVE (OMIM:611809) |
| ........Bietti Crystalline Dystrophy (C535440) |
| ........Bothnia Retinal Dystrophy (C564392) |
| ........Central Serous Chorioretinopathy (D056833) |
| ........Cerebroretinal Microangiopathy with Calcifications and Cysts (C567401) |
........Diabetic Retinopathy (D003930)  1 |
| ........Epiretinal Membrane (D019773) |
| ........Exudative Vitreoretinopathy 4 (C566619) |
| ........Exudative Vitreoretinopathy 5 (C567648) |
| ........Familial Exudative Vitreoretinopathy (C580083) |
| ........Fleck Retina, Familial Benign (C565564) |
| ........FLOTCH syndrome (C537065) |
| ........Fundus Albipunctatus (C562733) |
| ........Grouped Pigmentation of the Macula (C565530) |
| ........Hypertensive Retinopathy (D058437) |
| ........Iris hypoplasia and glaucoma (C535538) |
| ........Leber Congenital Amaurosis (D057130) 20 |
| ........Microcephaly with Chorioretinopathy, Autosomal Dominant (C563583) |
| ........Microcephaly with Chorioretinopathy, Autosomal Recessive (C565379) |
| ........MICROPHTHALMIA, ISOLATED 5 (OMIM:611040) |
| ........Oculomelic amyoplasia (C537737) |
| ........Rambaud Galian syndrome (C535283) |
| ........Ramos Arroyo Clark syndrome (C535286) |
| ........Retinal Aplasia (C566720) |
| ........Retinal Artery Occlusion (D015356) 1 |
| ........Retinal Degeneration (D012162) 195 |
| ........Retinal Detachment (D012163) 9 |
| ........Retinal Dysplasia (D015792) 2 |
| ........RETINAL DYSPLASIA, PRIMARY (OMIM:312550) |
| ........Retinal Hemorrhage (D012166) 2 |
| ........Retinal Neoplasms (D019572) 3 |
| ........Retinal Neovascularization (D015861) |
| ........Retinal Nonattachment, Nonsyndromic Congenital (C565633) |
| ........Retinal Perforations (D012167) |
| ........Retinal Telangiectasis (D058456) 1 |
| ........Retinal Vasculitis (D031300) 1 |
| ........Retinal Vein Occlusion (D012170) |
| ........Retinitis (D012173) 4 |
| ........Retinopathy of Prematurity (D012178) |
| ........Roifman syndrome (C535866) |
| ........Stickler Syndrome, Autosomal Recessive, COL9A1-Related (C565177) |
| ........Vasculopathy, Retinal, With Cerebral Leukodystrophy (C566007) |
| ........Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia (C565179) |
| ........Vitreoretinopathy, Proliferative (D018630) 5 |
Sister Nodes: |
..Asthenopia (D001248)
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..Cogan Syndrome (D055952) 2
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..Conjunctival Diseases (D003229) 29
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..Corneal Diseases (D003316) 120
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..Encephalocraniocutaneous lipomatosis (C535736)
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..Exudative Vitreoretinopathy 4 (C566619)
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..Exudative Vitreoretinopathy 5 (C567648)
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..Eye Abnormalities (D005124) 208
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..Eye Diseases, Hereditary (D015785) 373
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..Eye Hemorrhage (D005130) 6
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..Eye Infections (D015817) 25
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..Eye Injuries (D005131) 7
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..Eye Manifestations (D005132) 9
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..Eye Neoplasms (D005134) 20
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..Eyelid Diseases (D005141) 64
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..Hernandez Fragoso syndrome (C536062)
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..Lacrimal Apparatus Diseases (D007766) 18
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..Lens Diseases (D007905) 166
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..Mollica Pavone Antener syndrome (C535809)
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..MORM syndrome (C536984)
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..Neuropathy, Hereditary Sensorimotor, with Upper Motor Neuron, Visual Pathway and Autonomic Disturbance (C563517)
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..Ocular Hypertension (D009798) 52
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..Ocular Hypotension (D015814)
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..Ocular Motility Disorders (D015835) 109
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..Optic Nerve Diseases (D009901) 69
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..Orbital Diseases (D009916) 17
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..Pupil Disorders (D011681) 20
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..Refractive Errors (D012030) 57
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..Retinal Diseases (D012164) 287
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..Scleral Diseases (D015422) 3
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..Uveal Diseases (D014603) 59
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..Vision Disorders (D014786) 84
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..Vitreoretinopathy, Proliferative (D018630) 5
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..Vitreous Detachment (D020255) 1
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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