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myopia
(Q168403)
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From Wikidata
visual defect which causes to see the near objects clearly and far objects unclearly
near-sightedness
short-sightedness
near vision
edit
Language
Label
Description
Also known as
default for all languages
No label defined
–
English
myopia
visual defect which causes to see the near objects clearly and far objects unclearly
near-sightedness
short-sightedness
near vision
Statements
instance of
class of disease
0 references
symptom or sign
0 references
subclass of
refractive error
3 references
stated in
Analysis of genetic networks regulating refractive eye development in collaborative cross progenitor strain mice reveals new genes and pathways underlying human myopia
stated in
Global and regional estimates of prevalence of refractive errors: Systematic review and meta-analysis
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:11830
visual impairment
0 references
disease
0 references
image
Myopia.gif
400 × 308; 51 KB
0 references
health specialty
optometry
0 references
possible treatment
spherical lens
1 reference
imported from Wikimedia project
Japanese Wikipedia
genetic association
SNTB1
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=6641
http://www.genome.gov/gwastudies/index.cfm?gene=SNTB1
stated in
Phenocarta
Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia
retrieved
25 May 2020
VIPR2
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=7434
http://www.genome.gov/gwastudies/index.cfm?gene=VIPR2
stated in
Phenocarta
A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population
retrieved
25 May 2020
PLPPR5-AS1
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=100129620
http://www.genome.gov/gwastudies/index.cfm?gene=LOC100129620
stated in
Phenocarta
A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population
retrieved
25 May 2020
CAPN9
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=10753
http://www.genome.gov/gwastudies/index.cfm?gene=CAPN9
stated in
Phenocarta
A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population
retrieved
25 May 2020
FHIT
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=2272
http://www.genome.gov/gwastudies/index.cfm?gene=FHIT
stated in
Phenocarta
A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population
retrieved
25 May 2020
CLSTN2
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=64084
http://www.genome.gov/gwastudies/index.cfm?gene=CLSTN2
stated in
Phenocarta
A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population
retrieved
25 May 2020
DHX15
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=1665
http://www.genome.gov/gwastudies/index.cfm?gene=DHX15
stated in
Phenocarta
A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population
retrieved
25 May 2020
BMP6
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=654
http://www.genome.gov/gwastudies/index.cfm?gene=BMP6
stated in
Phenocarta
A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population
retrieved
25 May 2020
SRPK2
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=6733
http://www.genome.gov/gwastudies/index.cfm?gene=SRPK2
stated in
Phenocarta
A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population
retrieved
25 May 2020
PTPRN2
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=5799
http://www.genome.gov/gwastudies/index.cfm?gene=PTPRN2
stated in
Phenocarta
A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population
retrieved
25 May 2020
GATA4
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=2626
http://www.genome.gov/gwastudies/index.cfm?gene=GATA4
stated in
Phenocarta
A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population
retrieved
25 May 2020
PTPRD
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=5789
http://www.genome.gov/gwastudies/index.cfm?gene=PTPRD
stated in
Phenocarta
A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population
retrieved
25 May 2020
ABCA1
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=19
http://www.genome.gov/gwastudies/index.cfm?gene=ABCA1
stated in
Phenocarta
A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population
retrieved
25 May 2020
DENND1A
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=57706
http://www.genome.gov/gwastudies/index.cfm?gene=DENND1A
stated in
Phenocarta
A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population
retrieved
25 May 2020
TACC2
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=10579
http://www.genome.gov/gwastudies/index.cfm?gene=TACC2
stated in
Phenocarta
A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population
retrieved
25 May 2020
CNTN5
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=53942
http://www.genome.gov/gwastudies/index.cfm?gene=CNTN5
stated in
Phenocarta
A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population
retrieved
25 May 2020
FLI1
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=2313
http://www.genome.gov/gwastudies/index.cfm?gene=FLI1
stated in
Phenocarta
A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population
retrieved
25 May 2020
PML
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=5371
http://www.genome.gov/gwastudies/index.cfm?gene=PML
stated in
Phenocarta
A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population
retrieved
25 May 2020
DNAH9
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=1770
http://www.genome.gov/gwastudies/index.cfm?gene=DNAH9
stated in
Phenocarta
A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population
retrieved
25 May 2020
ZNF536
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=9745
http://www.genome.gov/gwastudies/index.cfm?gene=ZNF536
stated in
Phenocarta
A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population
retrieved
25 May 2020
SPTBN1
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=6711
http://www.genome.gov/gwastudies/index.cfm?gene=SPTBN1
stated in
Phenocarta
Genetic variants on chromosome 1q41 influence ocular axial length and high myopia
retrieved
25 May 2020
PARP8
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=79668
http://www.genome.gov/gwastudies/index.cfm?gene=PARP8
stated in
Phenocarta
Genetic variants on chromosome 1q41 influence ocular axial length and high myopia
retrieved
25 May 2020
CTNND2
determination method or standard
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=1501
http://www.genome.gov/gwastudies/index.cfm?gene=CTNND2
stated in
Phenocarta
Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese
retrieved
25 May 2020
PRIMPOL
1 reference
stated in
Exome sequencing reveals CCDC111 mutation associated with high myopia
LRPAP1
1 reference
stated in
Mutations in LRPAP1 are associated with severe myopia in humans
SLC39A5
1 reference
stated in
SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia
ZNF644
1 reference
stated in
Exome sequencing identifies ZNF644 mutations in high myopia
P3H2
1 reference
stated in
Open Targets Platform
retrieved
24 August 2023
reference URL
https://platform.opentargets.org/evidence/ENSG00000090530/Orphanet_98619
based on heuristic
inferred from an Open Targets association score over 0.7
SCO2
1 reference
stated in
Open Targets Platform
retrieved
24 August 2023
reference URL
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
statement is subject of
Q24348693
0 references
Small Brockhaus and Efron Encyclopedic Dictionary
statement is subject of
Q24755550
0 references
Jewish Encyclopedia of Brockhaus and Efron
statement is subject of
Q24950727
0 references
Meyers Konversations-Lexikon, 4th edition (1885–1890)
statement is subject of
Q112790169
0 references
Great Soviet Encyclopedia (1926–1947)
statement is subject of
Q111848845
0 references
Armenian Soviet Encyclopedia, vol. 5
page(s)
328
0 references
on focus list of Wikimedia project
WikiProject Medicine
0 references
ICD-9-CM
367.1
2 references
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
3 August 2018
Mondo ID
MONDO_0001384
ICPC 2 ID
F91
1 reference
imported from Wikimedia project
Spanish Wikipedia
NCI Thesaurus ID
C102533
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
exact match
http://purl.obolibrary.org/obo/DOID_11830
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:11830
http://identifiers.org/doid/DOID:11830
1 reference
stated in
Identifiers.org
reference URL
https://registry.identifiers.org/registry/doid
http://purl.obolibrary.org/obo/HP_0000545
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0000545
opposite of
hyperopia
0 references
Commons category
Myopia
1 reference
imported from Wikimedia project
Spanish Wikipedia
Identifiers
Bibliothèque nationale de France ID
12182153m
subject named as
Myopie
1 reference
stated in
Nuovo soggettario
reference URL
https://thes.bncf.firenze.sbn.it/termine.php?id=51019
retrieved
17 June 2021
GND ID
4073911-9
1 reference
imported from Wikimedia project
German Wikipedia
J9U ID
987007555752005171
1 reference
stated in
National Library of Israel
Library of Congress authority ID
sh85089271
subject named as
Myopia
1 reference
stated in
Integrated Authority File
NDL Authority ID
00565874
0 references
MeSH descriptor ID
D009216
mapping relation type
exact match
subject named as
Myopia
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
3 August 2018
Mondo ID
MONDO_0001384
MeSH tree code
C11.744.636
0 references
MedlinePlus ID
001023
1 reference
imported from Wikimedia project
English Wikipedia
PatientsLikeMe condition ID
myopia
0 references
KEGG ID
H02041
0 references
Australian Educational Vocabulary ID
scot/8051
0 references
Baidu Tieba name
高度近视
number of works
370,405
point in time
3 April 2023
0 references
近视
number of works
634,851
point in time
3 April 2023
0 references
BNCF Thesaurus ID
51019
1 reference
stated in
Nuovo soggettario
Cultureel Woordenboek ID
levenswetenschappen-en-geneeskunde/bijziendheid
0 references
Disease Ontology ID
DOID:11830
0 references
DiseasesDB
8729
1 reference
imported from Wikimedia project
English Wikipedia
Encyclopædia Britannica Online ID
science/myopia
subject named as
myopia
0 references
Encyclopedia of China (Third Edition) ID
91576
0 references
Freebase ID
/m/0m2w3
1 reference
stated in
Freebase Data Dumps
publication date
28 October 2013
Gran Enciclopèdia Catalana ID
miopia
0 references
Gran Enciclopèdia Catalana ID (former scheme)
0123890
0 references
0194503
0 references
0217950
0 references
Great Russian Encyclopedia Online ID (old version)
1873357
subject named as
БЛИЗОРУКОСТЬ
reason for deprecated rank
redirected to GRE portal
0 references
Great Russian Encyclopedia portal ID
blizorukost-5b0a48
0 references
Human Phenotype Ontology ID
HP:0000545
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
3 August 2018
Mondo ID
MONDO_0001384
ICD-10-CM
H52.1
2 references
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
3 August 2018
Mondo ID
MONDO_0001384
ICD-11 ID (Foundation)
1666440799
0 references
ICD-11 ID (MMS)
9D00.0
subject named as
Myopia
1 reference
Wikimedia import URL
https://www.wikidata.org/w/index.php?title=Wikidata:Property_proposal/ICD-11&oldid=1015857142
JSTOR topic ID (archived)
myopia
0 references
KBpedia ID
Nearsightedness
1 reference
stated in
KBpedia
retrieved
9 July 2020
Lex ID
nærsynethed
0 references
Mondo ID
MONDO_0001384
0 references
NHS Health A to Z ID
short-sightedness
0 references
OMIM ID
160700
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
255500
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
300613
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
310460
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
603221
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
608367
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
608474
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
608908
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
609256
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
609257
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
609258
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
609259
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
609994
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
609995
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
610320
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
612554
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
612717
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
613969
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
614166
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
614167
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
615420
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
615431
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
615946
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
Open Library subject ID
myopia
0 references
OpenAlex ID
C2992575515
1 reference
stated in
OpenAlex
retrieved
26 January 2022
reference URL
https://docs.openalex.org/download-snapshot/snapshot-data-format
Orphanet ID
98619
0 references
Quora topic ID
Myopia
1 reference
stated in
Quora
Store medisinske leksikon ID
nærsynthet
mapping relation type
exact match
subject named as
nærsynthet
1 reference
stated in
Great Norwegian Encyclopedia
retrieved
4 June 2020
UK Parliament thesaurus ID
454745
subject named as
Myopia
0 references
UMLS CUI
C0027092
2 references
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:11830
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0000545
C0027092
mapping relation type
close match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
3 August 2018
Mondo ID
MONDO_0001384
Vikidia article ID
fr:Myopie
0 references
WikiKids ID
Bijziendheid
0 references
WikiProjectMed ID
Near-sightedness
0 references
WikiSkripta article ID
41193
0 references
WordNet 3.1 Synset ID
14576882-n
1 reference
stated in
GF WordNet
YSO ID
5995
1 reference
stated in
YSO-Wikidata mapping project
Zhihu topic ID
19562874
subject named as
近视眼
0 references
Sitelinks
Wikipedia
(85 entries)
edit
afwiki
Miopie
anwiki
Miopía
arwiki
قصر النظر
aswiki
নিকটদৃষ্টি
azbwiki
یاخین-گؤرمک/مییوپی
azwiki
Miopiya (yaxındangörmə)
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Паніклівасьць
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Блізарукасць
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Kratkovidnost
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elwiki
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hywiki
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idwiki
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kkwiki
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kowiki
근시
kywiki
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Category:Myopia
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