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 473
Corneal disorder 105
Uveal disorder 95
Ocular growth disorder 84
Lens disorder 74
Eye neoplasm 73
Ocular vascular disorder 53
Eye degenerative disorder 47
Vitreous body disorder 43
Eye infectious disorder 35
Eyelid disorder 35
Glaucoma 29
Isolated anophthalmia-microphthalmia syndrome 26
Coloboma 22
Anterior segment dysgenesis 20
Hereditary optic neuropathy 19
Conjunctival disorder 13
Autoimmune/inflammatory optic neuropathy 12
Lacrimal apparatus disorder 12
Lamellar ichthyosis 7
Optic neuritis 7
Galactosemia 6
Gaucher disease 5
Ptosis 5
Rhizomelic chondrodysplasia punctata 5
Tay-Sachs disease 4
Refractive error 4
Scleral disorder 4
Alagille syndrome 3
GM1 gangliosidosis 3
LTBP2-related ocular dysgenesis 3
Sandhoff disease 3
Alpha-mannosidosis 3
Mucopolysaccharidosis type 1 3
Phakomatosis pigmentovascularis 3
Macular telangiectasia 2
Mucopolysaccharidosis type 6 2
Neuroocular syndrome 2
IgG4-related ophthalmic disorder 1
Eye accommodation disease 1
Isolated Pierre-Robin syndrome 1
Oculodentodigital dysplasia 1
9q33.3q34.11 microdeletion syndrome
Axenfeld anomaly
Cogan syndrome
Ehlers-Danlos syndrome, kyphoscoliotic type 1
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 segment developmental abnormality with extraocular manifestations
Atopic keratoconjunctivitis
Blindness - scoliosis - arachnodactyly syndrome
Cerebrotendinous xanthomatosis
Chondroectodermal dysplasia with night blindness
Congenital optic disk excavation
Ectodermal dysplasia-blindness syndrome
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
Megalocornea-intellectual disability syndrome
Mevalonic aciduria
Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome
Microcornea-glaucoma-absent frontal sinuses syndrome
Mucolipidosis type IV
Multiple evanescent white dot syndrome
Nail-patella syndrome
Neurotrophic keratopathy
Ocular cystinosis
Ocular motor apraxia, Cogan type
Oculocerebrorenal syndrome
Piebaldism
Pigment dispersion syndrome
Punctate inner choroidopathy
Stellate multiform amelanotic choroidopathy
Syndromic recessive X-linked ichthyosis
Toxic maculopathy due to antimalarial drugs
Tyrosinemia type II
Vernal keratoconjunctivitis
Visual snow syndrome

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