refractive error ^Béarla (Q470427)

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cause of vision problems ^Béarla

Language	Label	Description	Also known as
Gaeilge	No label defined	No description defined
Béarla	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

comhartha cliniciúil

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refraction or accommodation disorder ^Béarla

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sláinte na súl

1 reference

Disease Ontology ^Béarla

29 Samhain 2020

Disease Ontology ID ^Béarla

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gearrthóg fuaime

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

teanga an tsaothair nó an ainm

1 reference

https://lingualibre.org/wiki/Q636568

buaileann sé/sí

ocular refraction ^Béarla

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speisialtacht sláinte

oftailmeolaíocht

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genetic association ^Béarla

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

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

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

Phenocarta ^Béarla

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 ^Béarla

25 Bealtaine 2020

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

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

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

Phenocarta ^Béarla

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

25 Bealtaine 2020

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

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

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

Phenocarta ^Béarla

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

25 Bealtaine 2020

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

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

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

Phenocarta ^Béarla

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

25 Bealtaine 2020

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

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

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

Phenocarta ^Béarla

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

25 Bealtaine 2020

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

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

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

Phenocarta ^Béarla

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

25 Bealtaine 2020

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

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

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

Phenocarta ^Béarla

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

25 Bealtaine 2020

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

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

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

Phenocarta ^Béarla

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

25 Bealtaine 2020

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

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

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

Phenocarta ^Béarla

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

25 Bealtaine 2020

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

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

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

Phenocarta ^Béarla

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

25 Bealtaine 2020

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

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

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

Phenocarta ^Béarla

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

25 Bealtaine 2020

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

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

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

Phenocarta ^Béarla

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

25 Bealtaine 2020

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

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

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

Phenocarta ^Béarla

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

25 Bealtaine 2020

on focus list of Wikimedia project ^Béarla

WikiProject Medicine ^Béarla

0 references

NCI Thesaurus ID ^Béarla

C87145

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

exact match ^Béarla

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

1 reference

Disease Ontology ^Béarla

29 Samhain 2020

Disease Ontology ID ^Béarla

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

1 reference

Identifiers.org ^Béarla

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 ^Béarla

8 Deireadh Fómhair 2018

Human Phenotype Ontology ID ^Béarla

i gcontrárthacht le

emmetropia ^Béarla

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catagóir Commons

Refractive errors

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Identifiers

Bibliothèque nationale de France ID ^Béarla

Oeil -- Vices de réfraction

1 reference

Nuovo soggettario ^Béarla

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

16 Meitheamh 2021

NL CR AUT ID ^Béarla

refrakční vady oka

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MeSH descriptor ID ^Béarla

Refractive Errors

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

MeSH tree code ^Béarla

0 references

BNCF Thesaurus ID ^Béarla

1 reference

Nuovo soggettario ^Béarla

Disease Ontology ID ^Béarla

1 reference

Disease Ontology ^Béarla

29 Samhain 2020

Disease Ontology ID ^Béarla

DiseasesDB ^Béarla

1 reference

iompórtáilte ó thionscadal Vicipéide

Vicipéid an Bhéarla

Elhuyar ZTH ID ^Béarla

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Encyclopedia of China (Third Edition) ID ^Béarla

0 references

Freebase ID ^Béarla

1 reference

Freebase Data Dumps ^Béarla

dáta foilsithe

28 Deireadh Fómhair 2013

Great Russian Encyclopedia Online ID (old version) ^Béarla

АМЕТРОПИЯ

reason for deprecated rank ^Béarla

redirected to GRE portal ^Béarla

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Great Russian Encyclopedia portal ID ^Béarla

ametropiia-6e4a11

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Human Phenotype Ontology ID ^Béarla

1 reference

Human Phenotype Ontology release 2018-03-08 ^Béarla

8 Deireadh Fómhair 2018

Human Phenotype Ontology ID ^Béarla

ICD-10-CM ^Béarla

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

ICD-11 (foundation) ^Béarla

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ICD-11 ID (MMS) ^Béarla

9D00

Disorders of refraction

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ICD-9 ID ^Béarla

1 reference

iompórtáilte ó thionscadal Vicipéide

Vicipéid an Bhéarla

1 reference

iompórtáilte ó thionscadal Vicipéide

Vicipéid an Bhéarla

1 reference

iompórtáilte ó thionscadal Vicipéide

Vicipéid an Bhéarla

JSTOR topic ID ^Béarla

refractive-errors

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Microsoft Academic ID ^Béarla

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Mondo ID ^Béarla

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Online PWN Encyclopedia ID ^Béarla

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OpenAlex ID ^Béarla

1 reference

OpenAlex ^Béarla

26 Eanáir 2022

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

Orphanet ID ^Béarla

mapping relation type ^Béarla

exact match ^Béarla

1 reference

Monarch Disease Ontology release 2018-06-29 ^Béarla

28 Iúil 2018

Mondo ID ^Béarla

ID na topaice ar Quora

Refractive-Error

1 reference

Quora ^Béarla

Store medisinske leksikon ID ^Béarla

mapping relation type ^Béarla

exact match ^Béarla

0 references

UMLS CUI ^Béarla

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

1 reference

Human Phenotype Ontology release 2018-03-08 ^Béarla

8 Deireadh Fómhair 2018

Human Phenotype Ontology ID ^Béarla

1 reference

bunaithe ar chur chuige heorastúil

inferred by common Orphanet mappings on source and on Wikidata ^Béarla

UMLS 2023 ^Béarla

16 Meitheamh 2023

WikiProjectMed ID ^Béarla

Refractive error

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WordNet 3.1 Synset ID ^Béarla

14120206-n

1 reference

GF WordNet ^Béarla

YSO ID ^Béarla

1 reference

YSO-Wikidata mapping project ^Béarla

dáta foilsithe

5 Márta 2024

Sitelinks

Vicipéid(32 entries)

Wikibooks(0 entries)

Vicínuacht(0 entries)

Vicíshliocht(0 entries)

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Wikiversity(0 entries)

Vicíthaisteal(0 entries)

Wiktionary(0 entries)

Suíomhanna eile(1 entry)

commonswiki Category:Refractive errors

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