refractive error (Q470427)

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cause of vision problems

disorder of refraction
eye refraction disorder
refractive disorder
ametropia
refraction or accommodation disorder
refraction error
Abnormality of refraction
Refractive errors

Language	Label	Description	Also known as
English	refractive error	cause of vision problems	disorder of refraction eye refraction disorder refractive disorder ametropia refraction or accommodation disorder refraction error Abnormality of refraction Refractive errors

Statements

0 references

class of disease

0 references

visual impairment

0 references

refraction or accommodation disorder

0 references

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

0 references

pronunciation audio

LL-Q33810 (ori)-Psubhashish-ଚକ୍ଷୁ ପ୍ରତିସରଣ ଦୋଷ.wav
2.2 s; 211 KB

language of work or name

1 reference

https://lingualibre.org/wiki/Q636568

ocular refraction

0 references

health specialty

0 references

genetic association

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9835&ncbiId=54715

http://www.genome.gov/gwastudies/index.cfm?gene=RBFOX1

Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9835&ncbiId=776

http://www.genome.gov/gwastudies/index.cfm?gene=CACNA1D

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9835&ncbiId=3908

http://www.genome.gov/gwastudies/index.cfm?gene=LAMA2

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9835&ncbiId=79698

http://www.genome.gov/gwastudies/index.cfm?gene=ZMAT4

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9835&ncbiId=6096

http://www.genome.gov/gwastudies/index.cfm?gene=RORB

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9835&ncbiId=2893

http://www.genome.gov/gwastudies/index.cfm?gene=GRIA4

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9835&ncbiId=5923

http://www.genome.gov/gwastudies/index.cfm?gene=RASGRF1

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9835&ncbiId=4642

http://www.genome.gov/gwastudies/index.cfm?gene=MYO1D

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9835&ncbiId=55748

http://www.genome.gov/gwastudies/index.cfm?gene=CNDP2

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9835&ncbiId=56479

http://www.genome.gov/gwastudies/index.cfm?gene=KCNQ5

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9835&ncbiId=9414

http://www.genome.gov/gwastudies/index.cfm?gene=TJP2

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9835&ncbiId=5801

http://www.genome.gov/gwastudies/index.cfm?gene=PTPRR

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9835&ncbiId=388336

http://www.genome.gov/gwastudies/index.cfm?gene=SHISA6

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

25 May 2020

on focus list of Wikimedia project

WikiProject Medicine

0 references

NCI Thesaurus ID

C87145

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

http://purl.obolibrary.org/obo/DOID_9835

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:9835

1 reference

Identifiers.org

https://registry.identifiers.org/registry/doid

http://www.orpha.net/ORDO/Orphanet_98618

0 references

http://purl.obolibrary.org/obo/HP_0000539

1 reference

Human Phenotype Ontology release 2018-03-08

8 October 2018

Human Phenotype Ontology ID

0 references

Commons category

Refractive errors

0 references

Identifiers

Bibliothèque nationale de France ID

subject named as

Oeil -- Vices de réfraction

1 reference

Nuovo soggettario

https://thes.bncf.firenze.sbn.it/termine.php?id=40202

16 June 2021

subject named as

refrakční vady oka

0 references

MeSH descriptor ID

subject named as

Refractive Errors

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

0 references

BNCF Thesaurus ID

1 reference

Nuovo soggettario

Disease Ontology ID

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

1 reference

imported from Wikimedia project

English Wikipedia

0 references

Encyclopedia of China (Third Edition) ID

0 references

1 reference

Freebase Data Dumps

publication date

28 October 2013

Great Russian Encyclopedia Online ID (old version)

subject named as

АМЕТРОПИЯ

reason for deprecated rank

redirected to GRE portal

0 references

Great Russian Encyclopedia portal ID

ametropiia-6e4a11

0 references

Human Phenotype Ontology ID

1 reference

Human Phenotype Ontology release 2018-03-08

8 October 2018

Human Phenotype Ontology ID

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

ICD-11 ID (Foundation)

0 references

ICD-11 ID (MMS)

9D00

subject named as

Disorders of refraction

0 references

1 reference

imported from Wikimedia project

English Wikipedia

1 reference

imported from Wikimedia project

English Wikipedia

1 reference

imported from Wikimedia project

English Wikipedia

JSTOR topic ID (archived)

refractive-errors

0 references

Microsoft Academic ID

0 references

0 references

0 references

Online PWN Encyclopedia ID

0 references

1 reference

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

Refractive-Error

1 reference

Store medisinske leksikon ID

mapping relation type

0 references

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

1 reference

Human Phenotype Ontology release 2018-03-08

8 October 2018

Human Phenotype Ontology ID

1 reference

based on heuristic

inferred by common Orphanet mappings on source and on Wikidata

16 June 2023

WikiProjectMed ID

Refractive error

0 references

WordNet 3.1 Synset ID

14120206-n

1 reference

1 reference

YSO-Wikidata mapping project

publication date

5 March 2024

Sitelinks

Wikipedia(33 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(1 entry)

commonswiki Category:Refractive errors

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