List of MeSH codes (C11)
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The following is a partial list of the "C" codes for Medical Subject Headings (MeSH), as defined by the United States National Library of Medicine (NLM).
This list continues the information at List of MeSH codes (C10). Codes following these are found at List of MeSH codes (C12). For other MeSH codes, see List of MeSH codes.
The source for this content is the set of 2006 MeSH Trees from the NLM.
eye diseases
asthenopia
conjunctival diseases
- MeSH C11.187.183 – conjunctivitis
- conjunctivitis, allergic
- conjunctivitis, bacterial
- ophthalmia neonatorum
- MeSH C11.187.183.220.889 – trachoma
- conjunctivitis, viral
- keratoconjunctivitis, infectious
- keratoconjunctivitis sicca
- MeSH C11.187.781 – pterygium
- MeSH C11.187.810 – xerophthalmia
corneal diseases
- Fuchs' endothelial dystrophy
- MeSH C11.204.267 – corneal edema
- MeSH C11.204.299 – corneal opacity
- MeSH C11.204.299.070 – arcus senilis
- MeSH C11.204.564 – keratitis
- MeSH C11.204.564.225 – corneal ulcer
- keratoconjunctivitis, infectious
- keratoconjunctivitis sicca
- MeSH C11.204.627 – keratoconus
- MeSH C11.204.813 – trachoma
MeSH C11.250 – eye abnormalities
- MeSH C11.250.060 – aniridia
- MeSH C11.250.060.950 – WAGR syndrome
- anophthalmos
- MeSH C11.250.090 – blepharophimosis
- MeSH C11.250.110 – coloboma
- MeSH C11.250.300 – ectopia lentis
- hydrophthalmos
- microphthalmos
- MeSH C11.250.666 – retinal dysplasia
MeSH C11.270 – eye diseases, hereditary
- MeSH C11.270.040 – albinism
- albinism, ocular
- albinism, oculocutaneous
- MeSH C11.270.060 – aniridia
- MeSH C11.270.060.950 – WAGR syndrome
- MeSH C11.270.142 – choroideremia
- Fuchs' endothelial dystrophy
- duane retraction syndrome
- gyrate atrophy
- optic atrophies, hereditary
- optic atrophy, hereditary, leber
- optic atrophy, autosomal dominant
- MeSH C11.270.564.980 – Wolfram syndrome
- MeSH C11.270.660 – retinal dysplasia
- MeSH C11.270.684 – retinitis pigmentosa
- Usher syndromes
MeSH C11.290 – eye hemorrhage
- MeSH C11.290.195 – choroid hemorrhage
- MeSH C11.290.484 – hyphema
- retinal hemorrhage
- MeSH C11.290.960 – vitreous hemorrhage
MeSH C11.294 – eye infections
- MeSH C11.294.177 – corneal ulcer
- conjunctivitis, bacterial
- ophthalmia neonatorum
- MeSH C11.294.354.220.800 – trachoma
- hordeolum
- keratoconjunctivitis, infectious
- tuberculosis, ocular
- uveitis, suppurative
- uveitis, suppurative
- onchocerciasis, ocular
- toxoplasmosis, ocular
- MeSH C11.294.800 – eye infections, viral
- conjunctivitis, viral
MeSH C11.300 – eye manifestations
eye neoplasms
- eyelid neoplasms
- MeSH C11.319.457 – orbital neoplasms
- MeSH C11.319.475 – retinal neoplasms
- MeSH C11.319.475.760 – retinoblastoma
- uveal neoplasms
- MeSH C11.319.494.198 – choroid neoplasms
- MeSH C11.319.494.400 – iris neoplasms
eyelid diseases
- MeSH C11.338.133 – blepharitis
- MeSH C11.338.190 – blepharophimosis
- blepharoptosis
- MeSH C11.338.250 – blepharospasm
- MeSH C11.338.300 – chalazion
- MeSH C11.338.362 – ectropion
- MeSH C11.338.443 – entropion
- eyelid neoplasms
- hordeolum
Lacrimal apparatus diseases
- MeSH C11.496.221 – dacryocystitis
- MeSH C11.496.260 – dry eye syndromes
- keratoconjunctivitis sicca
- MeSH C11.496.260.719 – Sjögren syndrome
- MeSH C11.496.260.892 – xerophthalmia
lens diseases
- MeSH C11.510.103 – aphakia
- MeSH C11.510.245 – cataract
- lens subluxation
- MeSH C11.510.598.373 – ectopia lentis
MeSH C11.525 – ocular hypertension
- MeSH C11.525.381 – glaucoma
- hydrophthalmos
ocular hypotension
ocular motility disorders
- Duane retraction syndrome
- Miller Fisher syndrome
- nystagmus, pathologic
- nystagmus, congenital
- oculomotor nerve diseases
- MeSH C11.590.436.200 – Adie syndrome
- ophthalmoplegia
- ophthalmoplegia, chronic progressive external
- supranuclear palsy, progressive
- ophthalmoplegia, chronic progressive external
- MeSH C11.590.810 – strabismus
- MeSH C11.590.810.400 – esotropia
- MeSH C11.590.810.440 – exotropia
- MeSH C11.590.905 – Tolosa–Hunt syndrome
optic nerve diseases
- optic atrophy
- optic atrophies, hereditary
- optic atrophy, hereditary, leber
- optic atrophy, autosomal dominant
- optic disk drusen
- optic nerve injuries
- optic nerve neoplasms
- MeSH C11.640.576 – optic neuritis
- neuromyelitis optica
- optic neuropathy, ischemic
- MeSH C11.640.710 – papilledema
orbital diseases
- MeSH C11.675.319 – enophthalmos
- MeSH C11.675.349 – exophthalmos
- MeSH C11.675.349.500 – Graves' disease
- Graves ophthalmopathy
- MeSH C11.675.659 – orbital neoplasms
- retrobulbar hemorrhage
pupil disorders
- MeSH C11.710.090 – anisocoria
- MeSH C11.710.528 – miosis
- horner syndrome
- MeSH C11.710.570 – mydriasis
- tonic pupil
- MeSH C11.710.800.180 – aide syndrome
refractive errors
- MeSH C11.744.116 – aniseikonia
- MeSH C11.744.126 – anisometropia
- MeSH C11.744.212 – astigmatism
- hyperopia
- MeSH C11.744.636 – myopia
- MeSH C11.744.786 – presbyopia
retinal diseases
- MeSH C11.768.094 – angioid streaks
- MeSH C11.768.257 – diabetic retinopathy
- MeSH C11.768.328 – epiretinal membrane
- retinal artery occlusion
- MeSH C11.768.585 – retinal degeneration
- retinal drusen
- kearns-sayer syndrome
- usher syndromes
- MeSH C11.768.585.865 – retinoschisis
- MeSH C11.768.648 – retinal detachment
- MeSH C11.768.660 – retinal dysplasia
- retinal hemorrhage
- MeSH C11.768.717 – retinal neoplasms
- MeSH C11.768.717.760 – retinoblastoma
- MeSH C11.768.740 – retinal perforations
- MeSH C11.768.757 – retinal vasculitis
- retinal vein occlusion
- MeSH C11.768.773 – retinitis
- MeSH C11.768.773.348 – chorioretinitis
- retinal necrosis syndrome, acute
scleral diseases
- MeSH C11.790.500 – scleritis
uveal diseases
- choroid diseases
- MeSH C11.941.160.238 – choroid neoplasms
- MeSH C11.941.160.300 – choroideremia
- choroiditis
- pars planitis
- gyrate atrophy
- iris diseases
- MeSH C11.941.375.060 – aniridia
- MeSH C11.941.375.060.950 – WAGR syndrome
- exfoliation syndrome
- iridocyclitis
- MeSH C11.941.375.375 – iris neoplasms
- iritis
- uveal neoplasms
- MeSH C11.941.855.198 – choroid neoplasms
- MeSH C11.941.855.400 – iris neoplasms
- MeSH C11.941.879 – uveitis
- MeSH C11.941.879.780 – panuveitis
- ophthalmia, sympathetic
- uveitis, anterior
- behcet syndrome
- iridocyclitis
- iritis
- uveitis, posterior
- choroiditis
- pars planitis
- pars planitis
- uveitis, suppurative
- uveomeningoencephalitic syndrome
vision disorders
- MeSH C11.966.073 – amblyopia
- blindness
- MeSH C11.966.075.125 – amaurosis fugax
- blindness, cortical
- MeSH C11.966.075.500 – hemianopsia
- color vision defects
- MeSH C11.966.339 – diplopia
- night blindness
- MeSH C11.966.741 – photophobia
- MeSH C11.966.811 – scotoma
- vision, low
vitreous detachment
The list continues at List of MeSH codes (C12).