Medical Subject Headings
MeSH Tree Structures - 2013
C11 - Eye Diseases
- Eye Diseases [C11]
- Asthenopia [C11.093]
- Cogan Syndrome [C11.180]
- Conjunctival Diseases [C11.187]
- Conjunctival Neoplasms [C11.187.169]
- Conjunctivitis [C11.187.183]
- Pemphigoid, Benign Mucous Membrane [C11.187.482]
- Pinguecula [C11.187.631]
- Pterygium [C11.187.781]
- Xerophthalmia [C11.187.810]
- Corneal Diseases [C11.204]
- Corneal Dystrophies, Hereditary [C11.204.236]
- Corneal Edema [C11.204.267]
- Corneal Endothelial Cell Loss [C11.204.278]
- Corneal Neovascularization [C11.204.290]
- Corneal Opacity [C11.204.299]
- Corneal Perforation [C11.204.365]
- Corneal Wavefront Aberration [C11.204.431]
- Iridocorneal Endothelial Syndrome [C11.204.497]
- Keratitis [C11.204.564]
- Keratoconus [C11.204.627]
- Trachoma [C11.204.813]
- Eye Abnormalities [C11.250]
- Aniridia [C11.250.060]
- Anophthalmos [C11.250.080]
- Blepharophimosis [C11.250.090]
- Coloboma [C11.250.110]
- Ectopia Lentis [C11.250.300]
- Fraser Syndrome [C11.250.390]
- Hydrophthalmos [C11.250.480]
- Microphthalmos [C11.250.566]
- Persistent Hyperplastic Primary Vitreous [C11.250.616]
- Retinal Dysplasia [C11.250.666]
- Eye Diseases, Hereditary [C11.270]
- Aicardi Syndrome [C11.270.019]
- Albinism [C11.270.040]
- Aniridia [C11.270.060]
- Choroideremia [C11.270.142]
- Corneal Dystrophies, Hereditary [C11.270.162]
- Duane Retraction Syndrome [C11.270.235]
- Gyrate Atrophy [C11.270.468]
- Leber Congenital Amaurosis [C11.270.516]
- Optic Atrophies, Hereditary [C11.270.564]
- Retinal Dysplasia [C11.270.660]
- Retinitis Pigmentosa [C11.270.684]
- Graves Ophthalmopathy [C11.270.842]
- Walker-Warburg Syndrome [C11.270.881]
- Weill-Marchesani Syndrome [C11.270.921]
- Eye Hemorrhage [C11.290]
- Eye Infections [C11.294]
- Corneal Ulcer [C11.294.177]
- Endophthalmitis [C11.294.265]
- Eye Infections, Bacterial [C11.294.354]
- Eye Infections, Fungal [C11.294.450]
- Eye Infections, Parasitic [C11.294.725]
- Eye Infections, Viral [C11.294.800]
- Eye Injuries [C11.297]
- Eye Manifestations [C11.300]
- Eye Neoplasms [C11.319]
- Eyelid Diseases [C11.338]
- Lacrimal Apparatus Diseases [C11.496]
- Lens Diseases [C11.510]
- Ocular Hypertension [C11.525]
- Ocular Hypotension [C11.540]
- Ocular Motility Disorders [C11.590]
- Duane Retraction Syndrome [C11.590.224]
- Miller Fisher Syndrome [C11.590.312]
- Nystagmus, Pathologic [C11.590.400]
- Oculomotor Nerve Diseases [C11.590.436]
- Ophthalmoplegia [C11.590.472]
- Ophthalmoplegia, Chronic Progressive External [C11.590.641]
- Opsoclonus-Myoclonus Syndrome [C11.590.725]
- Strabismus [C11.590.810]
- Tolosa-Hunt Syndrome [C11.590.905]
- Optic Nerve Diseases [C11.640]
- Orbital Diseases [C11.675]
- Pupil Disorders [C11.710]
- Refractive Errors [C11.744]
- Retinal Diseases [C11.768]
- Angioid Streaks [C11.768.094]
- Central Serous Chorioretinopathy [C11.768.175]
- Diabetic Retinopathy [C11.768.257]
- Epiretinal Membrane [C11.768.328]
- Hypertensive Retinopathy [C11.768.346]
- Leber Congenital Amaurosis [C11.768.364]
- Retinal Artery Occlusion [C11.768.400]
- Retinal Degeneration [C11.768.585]
- Retinal Detachment [C11.768.648]
- Retinal Dysplasia [C11.768.660]
- Retinal Hemorrhage [C11.768.710]
- Retinal Neoplasms [C11.768.717]
- Retinal Neovascularization [C11.768.725]
- Retinal Perforations [C11.768.740]
- Retinal Telangiectasis [C11.768.748]
- Retinal Vasculitis [C11.768.757]
- Retinal Vein Occlusion [C11.768.760]
- Retinitis [C11.768.773]
- Retinopathy of Prematurity [C11.768.836]
- Vitreoretinopathy, Proliferative [C11.768.890]
- Scleral Diseases [C11.790]
- Uveal Diseases [C11.941]
- Choroid Diseases [C11.941.160]
- Iris Diseases [C11.941.375]
- Uveal Neoplasms [C11.941.855]
- Uveitis [C11.941.879]
- Vision Disorders [C11.966]
- Vitreoretinopathy, Proliferative [C11.975]
- Vitreous Detachment [C11.980]
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