loss of vision
Basic Information
- Identifier
- SYMP_0000321
- Notation
- SYMP:0000321
- Category
- symptoms
Related Diseases
- CEDNIK syndrome
- D-bifunctional protein deficiency
- Doyne honeycomb retinal dystrophy
- Fuchs' endothelial dystrophy
- GM1 gangliosidosis type 1
- GM2 gangliosidosis
- GM2 gangliosidosis, AB variant
- Krabbe disease
- Leber congenital amaurosis 7
- Leber plus disease
- Lisch epithelial corneal dystrophy
- McCune Albright syndrome
- NARP syndrome
- Norrie disease
- Peroxisome biogenesis disorder 7B
- Proteus syndrome
- Refsum disease
- Sandhoff disease
- Schindler disease
- Schindler disease type 1
- Stargardt disease
- Sveinsson chorioretinal atrophy
- Tay-Sachs disease
- Usher syndrome type 1C
- Usher syndrome type 1D
- Usher syndrome type 1E
- Usher syndrome type 1G
- Usher syndrome type 1J
- Usher syndrome type 1K
- WAGR syndrome
- Waardenburg syndrome type 2E
- acute disseminated encephalomyelitis
- acute endophthalmitis
- acute retinal necrosis syndrome
- acute retrobulbar neuritis
- adult brain stem glioma
- age related macular degeneration
- age related macular degeneration 1
- age related macular degeneration 10
- age related macular degeneration 11
- age related macular degeneration 12
- age related macular degeneration 13
- age related macular degeneration 14
- age related macular degeneration 15
- age related macular degeneration 2
- age related macular degeneration 5
- age related macular degeneration 6
- age related macular degeneration 8
- age related macular degeneration 9
- angle-closure glaucoma
- aqueous misdirection
- arteritic anterior ischemic optic neuropathy
- autoimmune uveitis
- autosomal dominant nonsyndromic deafness 28
- bilateral renal aplasia
- cavernous sinus thrombosis
- central pterygium
- cerebral lipidosis
- choroid disease
- chronic endophthalmitis
- cone-rod dystrophy 18
- congenital stromal corneal dystrophy
- conjunctival cancer
- conjunctival pterygium
- degeneration of macula and posterior pole
- dominant optic atrophy plus syndrome
- double pterygium
- exudative vitreoretinopathy
- eye carcinoma
- glaucomatous atrophy of optic disc
- glioblastoma
- globe disease
- gummatous syphilis
- hydrophthalmos
- hypersecretion glaucoma
- hypertensive retinopathy
- hypothalamic disease
- hypothalamic neoplasm
- inner ear cancer
- intermittent proptosis
- intracranial arteriosclerosis
- intracranial meningioma
- juvenile glaucoma
- late-adult onset retinitis pigmentosa
- leukoencephalopathy with vanishing white matter
- low tension glaucoma
- luxation of globe
- macular corneal dystrophy
- macular degeneration
- macular keratitis
- malignant oculomotor nerve tumor
- mitochondrial DNA depletion syndrome 20
- mitochondrial DNA depletion syndrome 4b
- mitochondrial DNA depletion syndrome 6
- mitochondrial complex I deficiency
- mitochondrial complex III deficiency
- mitochondrial complex V (ATP synthase) deficiency
- mitochondrial type mitochondrial complex I deficiency
- mitochondrial type mitochondrial complex I deficiency 1
- multiple mitochondrial dysfunctions syndrome
- multiple mitochondrial dysfunctions syndrome 2
- multiple mitochondrial dysfunctions syndrome 4
- multiple mitochondrial dysfunctions syndrome 6
- neovascular glaucoma
- neuritis
- neuromyelitis optica
- neuronal ceroid lipofuscinosis
- neuronal ceroid lipofuscinosis 1
- neuronal ceroid lipofuscinosis 10
- neuronal ceroid lipofuscinosis 2
- neuronal ceroid lipofuscinosis 7
- neuronal ceroid lipofuscinosis 8
- neuronal intranuclear inclusion disease
- neuroretinitis
- neurotrophic keratoconjunctivitis
- nodular degeneration of cornea
- nuclear type mitochondrial complex I deficiency 13
- nuclear type mitochondrial complex I deficiency 31
- obsolete CLN3 disease
- obsolete childhood supratentorial neoplasm
- obsolete choroidal rupture
- obsolete degenerative changes of ciliary body
- obsolete macular or paramacular focal retinitis and retinochoroiditis
- obsolete ocular toxoplasmosis
- obsolete papilledema associated with decreased ocular pressure
- obsolete papilledema associated with increased intracranial pressure
- obsolete primary retinal cyst
- obsolete relapsed retinoblastoma
- obsolete visual cortex disorder due to neoplasm
- ocular cancer
- oculocerebrorenal syndrome
- oculocutaneous albinism type V
- oculodentodigital dysplasia
- onchocerciasis
- optic atrophy
- optic atrophy 1
- optic atrophy 12
- optic atrophy 2
- optic atrophy 5
- optic disc anomalies with retinal and/or macular dystrophy
- optic nerve disease
- optic nerve neoplasm
- optic neuritis
- orbit rhabdomyosarcoma
- orbital cyst
- orbital granuloma
- orbital periostitis
- partial optic atrophy
- peroxisomal acyl-CoA oxidase deficiency
- peroxisome biogenesis disorder 11A
- peroxisome biogenesis disorder 1A
- phacolytic glaucoma
- pituitary adenoma 5
- posterior foramen magnum meningioma
- posterior uveal melanoma
- primary angle-closure glaucoma
- primary coenzyme Q10 deficiency 9
- primary intracranial sarcoma, DICER1-mutant
- primary optic atrophy
- progressive peripheral pterygium
- pseudopterygium
- pulsating exophthalmos
- residual stage angle-closure glaucoma
- retinal cancer
- retinal hemangioblastoma
- retinitis pigmentosa 10
- retinitis pigmentosa 12
- retinitis pigmentosa 20
- retinitis pigmentosa 22
- retinitis pigmentosa 29
- retinitis pigmentosa 59
- retinitis pigmentosa 61
- retinitis pigmentosa 63
- retinitis pigmentosa 87
- retinitis pigmentosa with or without situs inversus
- scleromalacia perforans
- strabismus
- syndromic microphthalmia 2
- toxascariasis
- uveal disease
- visual impairment and progressive phthisis bulbi
- vitelliform macular dystrophy
Medical Disclaimer: The information provided on this website is for general informational and educational purposes only.
It is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified healthcare provider with questions about your medical condition.