(Q168403)

Global and regional estimates of prevalence of refractive errors: Systematic review and meta-analysis.

30 November 2020

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Myopia.gif
400 × 308; 51 KB

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1 reference

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=6641

http://www.genome.gov/gwastudies/index.cfm?gene=SNTB1

Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia

25 May 2020

VIPR2

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=7434

http://www.genome.gov/gwastudies/index.cfm?gene=VIPR2

A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population

25 May 2020

PLPPR5-AS1

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=100129620

http://www.genome.gov/gwastudies/index.cfm?gene=LOC100129620

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population

25 May 2020

CAPN9

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=10753

http://www.genome.gov/gwastudies/index.cfm?gene=CAPN9

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population

25 May 2020

FHIT

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=2272

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

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population

25 May 2020

CLSTN2

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=64084

http://www.genome.gov/gwastudies/index.cfm?gene=CLSTN2

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population

25 May 2020

DHX15

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=1665

http://www.genome.gov/gwastudies/index.cfm?gene=DHX15

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population

25 May 2020

BMP6

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=654

http://www.genome.gov/gwastudies/index.cfm?gene=BMP6

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population

25 May 2020

SRPK2

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=6733

http://www.genome.gov/gwastudies/index.cfm?gene=SRPK2

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population

25 May 2020

PTPRN2

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=5799

http://www.genome.gov/gwastudies/index.cfm?gene=PTPRN2

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population

25 May 2020

GATA4

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=2626

http://www.genome.gov/gwastudies/index.cfm?gene=GATA4

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population

25 May 2020

PTPRD

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=5789

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

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population

25 May 2020

ABCA1

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=19

http://www.genome.gov/gwastudies/index.cfm?gene=ABCA1

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population

25 May 2020

DENND1A

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=57706

http://www.genome.gov/gwastudies/index.cfm?gene=DENND1A

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population

25 May 2020

TACC2

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=10579

http://www.genome.gov/gwastudies/index.cfm?gene=TACC2

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population

25 May 2020

CNTN5

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=53942

http://www.genome.gov/gwastudies/index.cfm?gene=CNTN5

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population

25 May 2020

FLI1

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=2313

http://www.genome.gov/gwastudies/index.cfm?gene=FLI1

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population

25 May 2020

PML

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=5371

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

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population

25 May 2020

DNAH9

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=1770

http://www.genome.gov/gwastudies/index.cfm?gene=DNAH9

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population

25 May 2020

ZNF536

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=9745

http://www.genome.gov/gwastudies/index.cfm?gene=ZNF536

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population

25 May 2020

SPTBN1

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=6711

http://www.genome.gov/gwastudies/index.cfm?gene=SPTBN1

Genetic variants on chromosome 1q41 influence ocular axial length and high myopia

25 May 2020

PARP8

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=79668

http://www.genome.gov/gwastudies/index.cfm?gene=PARP8

Genetic variants on chromosome 1q41 influence ocular axial length and high myopia

25 May 2020

CTNND2

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=1501

http://www.genome.gov/gwastudies/index.cfm?gene=CTNND2

Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese

25 May 2020

PRIMPOL

1 reference

Exome sequencing reveals CCDC111 mutation associated with high myopia

LRPAP1

1 reference

Mutations in LRPAP1 are associated with severe myopia in humans

SLC39A5

1 reference

SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia

ZNF644

1 reference

Exome sequencing identifies ZNF644 mutations in high myopia

P3H2

1 reference

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000090530/Orphanet_98619

based on heuristic

inferred from an Open Targets association score over 0.7

SCO2

1 reference

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000284194/Orphanet_98619

based on heuristic

inferred from an Open Targets association score over 0.7

described by source

Brockhaus and Efron Encyclopedic Dictionary

Small Brockhaus and Efron Encyclopedic Dictionary

Q24348693

0 references

Jewish Encyclopedia of Brockhaus and Efron

Q24755550

0 references

Meyers Konversations-Lexikon, 4th edition (1885–1890)

Q24950727

0 references

Great Soviet Encyclopedia (1926–1947)

Q112790169

0 references

Armenian Soviet Encyclopedia, vol. 5

Q111848845

0 references

page(s)

328

0 references

on focus list of Wikimedia project

WikiProject Medicine

0 references

ICD-9-CM

367.1

2 references

15 May 2019

3 August 2018

F91

1 reference

http://purl.obolibrary.org/obo/DOID_11830

Spanish Wikipedia

NCI Thesaurus ID

C102533

1 reference

15 May 2019

1 reference

30 November 2020

http://identifiers.org/doid/DOID:11830

1 reference

Identifiers.org

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

http://purl.obolibrary.org/obo/HP_0000545

1 reference

Human Phenotype Ontology release 2018-03-08

Human Phenotype Ontology ID

8 October 2018

0 references

Myopia

1 reference

Bibliothèque nationale de France ID

Spanish Wikipedia

Identifiers

12182153m

Myopie

1 reference

Nuovo soggettario

https://thes.bncf.firenze.sbn.it/termine.php?id=51019

17 June 2021

GND ID

4073911-9

1 reference

National Library of Israel J9U ID

German Wikipedia

987007555752005171

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National Library of Israel

Library of Congress authority ID

sh85089271

Myopia

1 reference

Integrated Authority File

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mapping relation type

exact match

Myopia

1 reference

3 August 2018

0 references

1 reference

PatientsLikeMe condition ID

English Wikipedia

myopia

0 references

KEGG ID

H02041

0 references

Australian Educational Vocabulary ID

0 references

370,405

3 April 2023

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近视

number of works

634,851

point in time

3 April 2023

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1 reference

Cultureel Woordenboek ID

levenswetenschappen-en-geneeskunde/bijziendheid

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1 reference

Encyclopædia Britannica Online ID

English Wikipedia

science/myopia

Encyclopedia of China (Third Edition) ID

myopia

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1 reference

28 October 2013

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Gran Enciclopèdia Catalana ID

miopia

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Gran Enciclopèdia Catalana ID (former scheme)

0123890

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0194503

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0217950

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Great Russian Encyclopedia Online ID (old version)

1873357

reason for deprecated rank

БЛИЗОРУКОСТЬ

redirected to GRE portal

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Great Russian Encyclopedia portal ID

blizorukost-5b0a48

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Human Phenotype Ontology ID

HP:0000545

1 reference

3 August 2018

2 references

15 May 2019

https://www.wikidata.org/w/index.php?title=Wikidata:Property_proposal/ICD-11&oldid=1015857142

3 August 2018

0 references

9D00.0

Myopia

1 reference

Wikimedia import URL

0 references

1 reference

9 July 2020

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1 reference

15 May 2019

1 reference

15 May 2019

1 reference

15 May 2019

1 reference

15 May 2019

1 reference

15 May 2019

1 reference

15 May 2019

1 reference

15 May 2019

1 reference

15 May 2019

1 reference

15 May 2019

1 reference

15 May 2019

1 reference

15 May 2019

1 reference

15 May 2019

1 reference

15 May 2019

1 reference

15 May 2019

1 reference

15 May 2019

1 reference

15 May 2019

1 reference

15 May 2019

1 reference

15 May 2019

1 reference

15 May 2019

1 reference

15 May 2019

1 reference

15 May 2019

1 reference

15 May 2019

1 reference

15 May 2019

Open Library subject ID

0 references

1 reference

26 January 2022

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

0 references

1 reference

Store medisinske leksikon ID

nærsynthet

mapping relation type

exact match

nærsynthet

1 reference

Great Norwegian Encyclopedia

UK Parliament thesaurus ID

4 June 2020

454745

Human Phenotype Ontology release 2018-03-08

Myopia

0 references

2 references

15 May 2019

Human Phenotype Ontology ID

8 October 2018

HP:0000545

C0027092

mapping relation type

close match

1 reference

YSO-Wikidata mapping project

3 August 2018

0 references

0 references

WikiSkripta article ID

41193

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WordNet 3.1 Synset ID

14576882-n

1 reference

1 reference

Zhihu topic ID

19562874