| class of disease | Q112193867 |
| degenerative disease | Q954257 |
| eye disease | Q3041498 |
| P1995 | health specialty | neurology | Q83042 |
| ophthalmology | Q161437 | ||
| P5008 | on focus list of Wikimedia project | WikiProject Medicine | Q4099686 |
| Q567820 | Alexander disease |
| Q1022718 | CADASIL |
| Q934034 | Chediak-Higashi syndrome |
| Q914389 | Cockayne syndrome |
| Q24977255 | Corneal-cerebellar syndrome |
| Q190564 | Huntington's disease |
| Q511372 | Krabbe disease |
| Q6441908 | Kufor-Rakeb syndrome |
| Q16965307 | Neonatal adrenoleukodystrophy |
| Q2067267 | Niemann–Pick disease, type C |
| Q4357091 | PEHO syndrome |
| Q1876206 | Pelizaeus-Merzbacher disease |
| Q917227 | Sandhoff disease |
| Q560337 | Tay-Sachs disease |
| Q189167 | Zellweger syndrome |
| Q337604 | aceruloplasminemia |
| Q29982071 | autosomal dominant optic atrophy |
| Q4826996 | autosomal recessive cerebellar ataxia |
| Q55345904 | autosomal recessive isolated optic atrophy |
| Q18554170 | blind hypertensive eye |
| Q18558226 | choroidal sclerosis |
| Q18553789 | conjunctival degeneration |
| Q18554311 | corneal degeneration |
| Q3508677 | deafness dystonia syndrome |
| Q18554189 | degenerative myopia |
| Q55345749 | early-onset X-linked optic atrophy |
| Q55345878 | early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome |
| Q18553781 | eyelid degenerative disease |
| Q55346022 | fatty acid hydroxylase-associated neurodegeneration |
| Q18553842 | glaucomatous atrophy of optic disc |
| Q32142710 | hereditary spastic paraplegia 2 |
| Q3363626 | hereditary spastic paraplegia 7 |
| Q32143434 | hereditary spastic paraplegia 9A |
| Q28065598 | hypomyelinating leukodystrophy 5 |
| Q18553533 | infantile cerebellar-retinal degeneration |
| Q55346060 | infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome |
| Q1862805 | leukocoria |
| Q55345817 | microphthalmia-brain atrophy syndrome |
| Q26492829 | multiple mitochondrial dysfunctions syndrome 4 |
| Q55345664 | muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome |
| Q32140736 | neurodegeneration with brain iron accumulation 4 |
| Q611458 | neuromyelitis optica |
| Q4358039 | neuronal ceroid lipofuscinosis |
| Q55345828 | optic atrophy 7 |
| Q55345985 | osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome |
| Q1436162 | pantothenate kinase-associated neurodegeneration |
| Q945930 | progressive supranuclear palsy |
| Q3043268 | retinal degeneration |
| Q2964435 | rhizomelic chondrodysplasia punctata type 1 |
| Q18554164 | siderosis of eye |
| Q55345684 | snowflake vitreoretinal degeneration |
| Q55346049 | spastic paraplegia-optic atrophy-neuropathy and spastic paraplegia-optic atrophy-neuropathy-related disorder |
| Q899726 | spinocerebellar ataxia |
| Q55346056 | tremor-ataxia-central hypomyelination syndrome |
| Q18554183 | vitreous syneresis |
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