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망막색소변성증 · Vinony

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Blindness
망막색소변성증

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EntityQ847057· pop 37· linked from 652 articles

망막색소변성증

Also known as RP, pericentral pigmentary retinopathy, pigmentary degeneration of the retina, Retinitis pigmentosa, retinal degeneration

retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss

Key facts

Other names: Inherited retinal dystrophy/diseases
Specialty: Ophthalmology , Optometry
Symptoms: Trouble seeing at night , decreased peripheral vision
Usual onset: Childhood
Causes: Genetic
Diagnostic method: Eye examination
Treatment: Low vision aids , portable lighting, orientation and mobility training
Frequency: 1 in 4,000 people

via Wikipedia infobox

Research

16,252 papers

[Retinitis pigmentosa].Revue medicale de Liege · 2020
Retinitis pigmentosa.

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Connections

visual impairment

Categories

Blindness Channelopathies Disorders of choroid and retina

Sources

wikipedia.externallinksexternallink

Survey of ophthalmology · 1988

X-Linked Retinitis Pigmentosa.Advances in experimental medicine and biology · 2025

Autosomal Dominant Retinitis Pigmentosa.Advances in experimental medicine and biology · 2018

Retinitis pigmentosa.British medical journal (Clinical research ed.) · 1981

Wikidata facts

Official website: rp-israel.org.il
Image: Fundus of patient with retinitis pigmentosa, mid stage.jpg

Show 4 more facts

NCI Thesaurus ID: C85045
Commons category: Retinitis pigmentosa
exact match: www.orpha.net/ORDO/Orphanet_791
external data available at URL: www.nanbyou.or.jp/entry/196

Sources (6)

wikidata.org
patient.co.uk
ddrare.nibiohn.go.jp
en.wikipedia.org
docs.openalex.org
he.wikipedia.org

via Wikidata · CC0

Show 17 more

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via Wikidata sitelinks · CC0

gene

Entity

mitochondrial DNA

congenital disorder

Online Mendelian Inheritance in Man

genetic testing

ophthalmoplegia

chorioretinitis

Leber congenital amaurosis

optic nerve disease

progressive retinal atrophy

International Standard Book Number

Alzheimer's disease

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Similar entities

Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).

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vitelliform macular dystrophy

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Leber congenital amaurosis

Entitydist 0.47

diabetic retinopathy

Entitydist 0.48

Entitydist 0.51

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Entitydist 0.51

Proteindist 0.52

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