mióipe (Q168403)

Analysis of genetic networks regulating refractive eye development in collaborative cross progenitor strain mice reveals new genes and pathways underlying human myopia ^Béarla

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

Disease Ontology ^Béarla

30 Samhain 2020

Disease Ontology ID ^Béarla

0 references

0 references

Myopia.gif
400 × 308; 51 KB

0 references

speisialtacht sláinte

optaiméadracht

0 references

cóireáil

spherical lens ^Béarla

1 reference

Vicipéid na Seapáinise

genetic association ^Béarla

SNTB1

determination method ^Béarla

TAS ^Béarla

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 ^Béarla

Phenocarta ^Béarla

25 Bealtaine 2020

VIPR2

determination method ^Béarla

TAS ^Béarla

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 ^Béarla

Phenocarta ^Béarla

25 Bealtaine 2020

PLPPR5-AS1

determination method ^Béarla

TAS ^Béarla

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 ^Béarla

Phenocarta ^Béarla

25 Bealtaine 2020

CAPN9

determination method ^Béarla

TAS ^Béarla

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 ^Béarla

Phenocarta ^Béarla

25 Bealtaine 2020

FHIT

determination method ^Béarla

TAS ^Béarla

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 ^Béarla

Phenocarta ^Béarla

25 Bealtaine 2020

CLSTN2

determination method ^Béarla

TAS ^Béarla

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 ^Béarla

Phenocarta ^Béarla

25 Bealtaine 2020

DHX15

determination method ^Béarla

TAS ^Béarla

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 ^Béarla

Phenocarta ^Béarla

25 Bealtaine 2020

BMP6

determination method ^Béarla

TAS ^Béarla

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 ^Béarla

Phenocarta ^Béarla

25 Bealtaine 2020

SRPK2

determination method ^Béarla

TAS ^Béarla

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 ^Béarla

Phenocarta ^Béarla

25 Bealtaine 2020

PTPRN2

determination method ^Béarla

TAS ^Béarla

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 ^Béarla

Phenocarta ^Béarla

25 Bealtaine 2020

GATA4

determination method ^Béarla

TAS ^Béarla

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 ^Béarla

Phenocarta ^Béarla

25 Bealtaine 2020

PTPRD

determination method ^Béarla

TAS ^Béarla

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 ^Béarla

Phenocarta ^Béarla

25 Bealtaine 2020

ABCA1

determination method ^Béarla

TAS ^Béarla

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 ^Béarla

Phenocarta ^Béarla

25 Bealtaine 2020

DENND1A

determination method ^Béarla

TAS ^Béarla

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 ^Béarla

Phenocarta ^Béarla

25 Bealtaine 2020

TACC2

determination method ^Béarla

TAS ^Béarla

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 ^Béarla

Phenocarta ^Béarla

25 Bealtaine 2020

CNTN5

determination method ^Béarla

TAS ^Béarla

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 ^Béarla

Phenocarta ^Béarla

25 Bealtaine 2020

FLI1

determination method ^Béarla

TAS ^Béarla

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 ^Béarla

Phenocarta ^Béarla

25 Bealtaine 2020

PML

determination method ^Béarla

TAS ^Béarla

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 ^Béarla

Phenocarta ^Béarla

25 Bealtaine 2020

DNAH9

determination method ^Béarla

TAS ^Béarla

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 ^Béarla

Phenocarta ^Béarla

25 Bealtaine 2020

ZNF536

determination method ^Béarla

TAS ^Béarla

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 ^Béarla

Phenocarta ^Béarla

25 Bealtaine 2020

SPTBN1

determination method ^Béarla

TAS ^Béarla

1 reference

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

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

Phenocarta ^Béarla

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

25 Bealtaine 2020

PARP8

determination method ^Béarla

TAS ^Béarla

1 reference

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

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

Phenocarta ^Béarla

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

25 Bealtaine 2020

CTNND2

determination method ^Béarla

TAS ^Béarla

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 ^Béarla

Phenocarta ^Béarla

25 Bealtaine 2020

PRIMPOL

1 reference

Exome sequencing reveals CCDC111 mutation associated with high myopia ^Béarla

LRPAP1

1 reference

Mutations in LRPAP1 are associated with severe myopia in humans ^Béarla

SLC39A5

1 reference

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

ZNF644

1 reference

Exome sequencing identifies ZNF644 mutations in high myopia ^Béarla

P3H2

1 reference

Open Targets Platform ^Béarla

24 Lúnasa 2023

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

bunaithe ar chur chuige heorastúil

inferred from an Open Targets association score over 0.7 ^Béarla

SCO2

1 reference

Open Targets Platform ^Béarla

24 Lúnasa 2023

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

bunaithe ar chur chuige heorastúil

inferred from an Open Targets association score over 0.7 ^Béarla

cur síos ag an bhfoinse

Brockhaus and Efron Encyclopedic Dictionary ^Béarla

Q24348693

0 references

Small Brockhaus and Efron Encyclopedic Dictionary ^Béarla

Q24755550

0 references

Jewish Encyclopedia of Brockhaus and Efron ^Béarla

Q24950727

0 references

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

Q112790169

0 references

Great Soviet Encyclopedia (1926–1947) ^Béarla

Q111848845

0 references

Armenian Soviet Encyclopedia, vol. 5 ^Béarla

leathanach

328

0 references

on focus list of Wikimedia project ^Béarla

WikiProject Medicine ^Béarla

0 references

ICD-9-CM ^Béarla

367.1

2 references

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

Monarch Disease Ontology release 2018-06-29 ^Béarla

3 Lúnasa 2018

Mondo ID ^Béarla

ICPC 2 ID ^Béarla

F91

1 reference

Vicipéid na Spáinnise

NCI Thesaurus ID ^Béarla

C102533

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

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

meaitseáil chruinn

1 reference

Disease Ontology ^Béarla

30 Samhain 2020

Disease Ontology ID ^Béarla

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

1 reference

Identifiers.org ^Béarla

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

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

1 reference

Human Phenotype Ontology release 2018-03-08 ^Béarla

8 Deireadh Fómhair 2018

Human Phenotype Ontology ID ^Béarla

0 references

Myopia

1 reference

Vicipéid na Spáinnise

Identifiers

Bibliothèque nationale de France ID ^Béarla

12182153m

Myopie

1 reference

Nuovo soggettario ^Béarla

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

17 Meitheamh 2021

ID GND

4073911-9

1 reference

Vicipéid na Gearmáinise

National Library of Israel J9U ID ^Béarla

987007555752005171

1 reference

Leabharlann Náisiúnta Iosrael

aitheantóir LoC

sh85089271

Myopia

1 reference

Integrated Authority File ^Béarla

NDL Authority ID ^Béarla

00565874

0 references

MeSH descriptor ID ^Béarla

D009216

mapping relation type ^Béarla

meaitseáil chruinn

Myopia

1 reference

Monarch Disease Ontology release 2018-06-29 ^Béarla

3 Lúnasa 2018

Mondo ID ^Béarla

MeSH tree code ^Béarla

C11.744.636

0 references

ID MedlinePlus

001023

1 reference

Vicipéid an Bhéarla

PatientsLikeMe condition ID ^Béarla

myopia

0 references

KEGG ID ^Béarla

H02041

0 references

Australian Educational Vocabulary ID ^Béarla

scot/8051

0 references

Baidu Tieba name ^Béarla

高度近视

number of works ^Béarla

370,405

am

3 Aibreán 2023

0 references

近视

number of works ^Béarla

634,851

am

3 Aibreán 2023

0 references

BNCF Thesaurus ID ^Béarla

51019

1 reference

levenswetenschappen-en-geneeskunde/bijziendheid

Nuovo soggettario ^Béarla

Cultureel Woordenboek ID ^Béarla

0 references

Den Store Danske ID ^Béarla

nærsynethed

0 references

Disease Ontology ID ^Béarla

0 references

DiseasesDB ^Béarla

8729

1 reference

Vicipéid an Bhéarla

Encyclopædia Britannica Online ID ^Béarla

science/myopia

myopia

0 references

Encyclopedia of China (Third Edition) ID ^Béarla

91576

0 references

Freebase ID ^Béarla

/m/0m2w3

1 reference

ID Gran Enciclopèdia Catalana

Freebase Data Dumps ^Béarla

dáta foilsithe

28 Deireadh Fómhair 2013

Gran Enciclopèdia Catalana ID ^Béarla

miopia

0 references

0123890

0 references

0194503

0 references

0217950

0 references

Great Russian Encyclopedia Online ID (old version) ^Béarla

1873357

БЛИЗОРУКОСТЬ

an chúis ar dímholadh é

redirected to GRE portal ^Béarla

0 references

Great Russian Encyclopedia portal ID ^Béarla

blizorukost-5b0a48

0 references

Human Phenotype Ontology ID ^Béarla

HP:0000545

1 reference

Monarch Disease Ontology release 2018-06-29 ^Béarla

3 Lúnasa 2018

Mondo ID ^Béarla

ICD-10-CM ^Béarla

H52.1

2 references

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

Monarch Disease Ontology release 2018-06-29 ^Béarla

3 Lúnasa 2018

Mondo ID ^Béarla

ICD-11 ID (Foundation) ^Béarla

1666440799

0 references

ICD-11 ID (MMS) ^Béarla

9D00.0

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

Myopia

1 reference

Wikimedia import URL ^Béarla

JSTOR topic ID ^Béarla

myopia

0 references

KBpedia ID ^Béarla

1 reference

9 Iúil 2020

Mondo ID ^Béarla

0 references

NHS Health A to Z ID ^Béarla

short-sightedness

0 references

OMIM ID ^Béarla

160700

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

255500

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

300613

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

310460

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

603221

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

608367

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

608474

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

608908

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

609256

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

609257

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

609258

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

609259

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

609994

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

609995

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

610320

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

612554

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

612717

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

613969

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

614166

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

614167

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

615420

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

615431

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

615946

1 reference

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

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

Open Library subject ID ^Béarla

myopia

0 references

OpenAlex ID ^Béarla

1 reference

26 Eanáir 2022

Orphanet ID ^Béarla

98619

0 references

ID na topaice ar Quora

Myopia

1 reference

Quora

Store medisinske leksikon ID ^Béarla

nærsynthet

mapping relation type ^Béarla

meaitseáil chruinn

nærsynthet

1 reference

Great Norwegian Encyclopedia ^Béarla

4 Meitheamh 2020

UK Parliament thesaurus ID ^Béarla

454745

Myopia

0 references

UMLS CUI ^Béarla

C0027092

2 references

Disease Ontology ^Béarla

15 Bealtaine 2019

Disease Ontology ID ^Béarla

Human Phenotype Ontology release 2018-03-08 ^Béarla

8 Deireadh Fómhair 2018

Human Phenotype Ontology ID ^Béarla

HP:0000545

C0027092

mapping relation type ^Béarla

close match ^Béarla

1 reference

Monarch Disease Ontology release 2018-06-29 ^Béarla

3 Lúnasa 2018

Mondo ID ^Béarla

Vikidia article ID ^Béarla

fr:Myopie

0 references

WikiKids ID ^Béarla

Bijziendheid

0 references

WikiProjectMed ID ^Béarla

Near-sightedness

0 references

WikiSkripta article ID ^Béarla

41193

0 references

WordNet 3.1 Synset ID ^Béarla

14576882-n

1 reference

GF WordNet ^Béarla

YSO ID ^Béarla

5995

1 reference

YSO-Wikidata mapping project ^Béarla

Zhihu topic ID ^Béarla

19562874