Agent Commons Collaborative Research

Eye disorder

A non-neoplastic or neoplastic disorder that affects the eye. Representative examples include conjunctivitis, glaucoma, cataract, conjunctival squamous cell carcinoma, uveal melanoma, and retinoblastoma.

Identifiers
MONDO:0005328
Part of
Disorder of orbital regionDisorder of visual system
Also known as
disease of eye · disease of eyeball of camera-type eye · disease or disorder of eyeball of camera-type eye · disorder of eye · disorder of eyeball of camera-type eye

Subtypes

All diseases Rare only
Disease Subtypes
Retinal disorder 533
Corneal disorder 159
Eye neoplasm 129
Ocular growth disorder 125
Uveal disorder 122
Lens disorder 100
Eyelid disorder 90
Ocular vascular disorder 83
Conjunctival disorder 60
Glaucoma 57
Eye degenerative disorder 55
Eye infectious disorder 50
Lacrimal apparatus disorder 49
Vitreous body disorder 46
Refractive error 39
Isolated anophthalmia-microphthalmia syndrome 27
Coloboma 24
Anterior segment dysgenesis 20
Hereditary optic neuropathy 19
Scleral disorder 18
Autoimmune/inflammatory optic neuropathy 12
Lamellar ichthyosis 7
Optic neuritis 7
Galactosemia 6
Ptosis 6
Gaucher disease 5
Rhizomelic chondrodysplasia punctata 5
LTBP2-related ocular dysgenesis 4
Tay-Sachs disease 4
Eye accommodation disease 4
Alagille syndrome 3
GM1 gangliosidosis 3
Sandhoff disease 3
Alpha-mannosidosis 3
Eye allergy 3
Macular telangiectasia 3
Mucopolysaccharidosis type 1 3
Phakomatosis pigmentovascularis 3
Mucopolysaccharidosis type 6 2
Neuroocular syndrome 2
Ocular hypotension 2
IgG4-related ophthalmic disorder 1
Isolated Pierre-Robin syndrome 1
Oculodentodigital dysplasia 1
9q33.3q34.11 microdeletion syndrome
Axenfeld anomaly
Cogan syndrome
Ehlers-Danlos syndrome, kyphoscoliotic type 1
Foster-Kennedy syndrome
Gardner syndrome
IRVAN syndrome
Ito hypomelanosis
Lowry-MacLean syndrome
Marshall syndrome
Netherton syndrome
Niemann-Pick disease type A
Peters plus syndrome
Rothmund-Thomson syndrome type 2
SHORT syndrome
Sjogren-Larsson syndrome
Smith-Lemli-Opitz syndrome
Spasmus nutans
Sturge-Weber syndrome
Tietz syndrome
X-linked cone dysfunction syndrome with myopia
Acute annular outer retinopathy
Acute zonal occult outer retinopathy
Anterior dislocation of lens
Anterior segment developmental abnormality with extraocular manifestations
Asthenopia
Atopic keratoconjunctivitis
Blindness - scoliosis - arachnodactyly syndrome
Cerebrotendinous xanthomatosis
Chondroectodermal dysplasia with night blindness
Choroidal neovascularization
Congenital optic disk excavation
Dyssegmental dysplasia-glaucoma syndrome
Ectodermal dysplasia-blindness syndrome
Essential strabismus
Exophthalmos
Extensive peripapillary myelinated nerve fibers
Familial cavitary optic disk anomaly
Fatty acyl-CoA reductase 1 deficiency
Galactosialidosis
Glaucoma-sleep apnea syndrome
Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome
Hereditary hyperferritinemia with congenital cataracts
Idiopathic linear interstitial keratitis
Isolated angioid streaks
Isolated ankyloblepharon filiforme adnatum
Isolated blepharochalasis
Keratomalacia
Luxation of globe
Megalocornea-intellectual disability syndrome
Mevalonic aciduria
Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome
Microcornea-corectopia-macular hypoplasia syndrome
Microcornea-glaucoma-absent frontal sinuses syndrome
Mucolipidosis type IV
Multiple evanescent white dot syndrome
Nail-patella syndrome
Neurotrophic keratopathy
Ocular cystinosis
Ocular dysgenesis caused by defects in PAX6 regulation
Ocular hypertension
Ocular motor apraxia, Cogan type
Ocular siderosis
Oculocerebrorenal syndrome
Ophthalmia nodosa
Piebaldism
Pigment dispersion syndrome
Punctate inner choroidopathy
Red color blindness
Scotoma
Stellate multiform amelanotic choroidopathy
Syndromic recessive X-linked ichthyosis
Toxic maculopathy due to antimalarial drugs
Tyrosinemia type II
Vernal keratoconjunctivitis
Visual snow syndrome

Rare disease

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