vitiligo (Q180152)

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hypersensitivity reaction type II disease that causes depigmentation of skin patches resulting from loss of function or death of melanocytes

Language	Label	Description	Also known as
English	vitiligo	hypersensitivity reaction type II disease that causes depigmentation of skin patches resulting from loss of function or death of melanocytes

Statements

class of disease

0 references

autoimmune disease

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

autoimmune skin disease

2 references

Monarch Disease Ontology release 2018-06-29

28 July 2018

Disease Ontology

30 November 2020

Disease Ontology ID

0 references

Ferguson Day 7, Picture 8 (cropped).png
180 × 240; 76 KB

1 reference

imported from Wikimedia project

Dutch Wikipedia

Wikimedia import URL

https://nl.wikipedia.org/w/index.php?title=Vitiligo&oldid=53224124

biology of colour

0 references

health specialty

0 references

symptoms and signs

0 references

drug or therapy used for treatment

1 reference

language of work or name

13 December 2016

1 reference

language of work or name

13 December 2016

1 reference

language of work or name

13 December 2016

genetic association

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_12306&ncbiId=4026

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

Association analyses identify three susceptibility Loci for vitiligo in the Chinese Han population

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_12306&ncbiId=60468

http://www.genome.gov/gwastudies/index.cfm?gene=BACH2

Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_12306&ncbiId=840

http://www.genome.gov/gwastudies/index.cfm?gene=CASP7

Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_12306&ncbiId=64375

http://www.genome.gov/gwastudies/index.cfm?gene=IKZF4

Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_12306&ncbiId=148022

http://www.genome.gov/gwastudies/index.cfm?gene=TICAM1

Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_12306&ncbiId=57178

http://www.genome.gov/gwastudies/index.cfm?gene=ZMIZ1

Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_12306&ncbiId=473

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

Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_12306&ncbiId=7299

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

Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_12306&ncbiId=3002

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

Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_12306&ncbiId=53347

http://www.genome.gov/gwastudies/index.cfm?gene=UBASH3A

Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_12306&ncbiId=114904

http://www.genome.gov/gwastudies/index.cfm?gene=C1QTNF6

Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_12306&ncbiId=64094

http://www.genome.gov/gwastudies/index.cfm?gene=SMOC2

Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_12306&ncbiId=5205

http://www.genome.gov/gwastudies/index.cfm?gene=ATP8B1

Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8

25 May 2020

1 reference

UniProt protein ID

13 August 2019

described by source

Great Soviet Encyclopedia (1926–1947)

statement is subject of

0 references

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

statement is subject of

0 references

on focus list of Wikimedia project

WikiProject Medicine

0 references

709.01

2 references

Disease Ontology

15 May 2019

Disease Ontology ID

Monarch Disease Ontology release 2018-06-29

28 July 2018

NCI Thesaurus ID

C26915

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

http://purl.obolibrary.org/obo/DOID_12306

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:12306

1 reference

Identifiers.org

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

http://purl.obolibrary.org/obo/HP_0001045

1 reference

Human Phenotype Ontology release 2018-03-08

8 October 2018

Human Phenotype Ontology ID

http://www.orpha.net/ORDO/Orphanet_247871

0 references

said to be the same as

0 references

Commons category

Vitiligo

0 references

Identifiers

Bibliothèque nationale de France ID

subject named as

Vitiligo

1 reference

Nuovo soggettario

https://thes.bncf.firenze.sbn.it/termine.php?id=23984

15 June 2021

0 references

987007543704105171

1 reference

National Library of Israel

Library of Congress authority ID

0 references

National Library of Latvia ID

0 references

subject named as

vitiligo

0 references

MeSH descriptor ID

mapping relation type

subject named as

Vitiligo

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

C17.800.621.440.895

0 references

1 reference

imported from Wikimedia project

English Wikipedia

PatientsLikeMe condition ID

0 references

0 references

1 reference

BNCF Thesaurus ID

1 reference

Nuovo soggettario

0 references

Disease Ontology ID

0 references

1 reference

imported from Wikimedia project

English Wikipedia

1 reference

imported from Wikimedia project

English Wikipedia

Encyclopædia Britannica Online ID

science/vitiligo

subject named as

vitiligo

0 references

Encyclopædia Universalis ID

0 references

Encyclopedia of China (Third Edition) ID

0 references

Experimental Factor Ontology ID

1 reference

based on heuristic

inferred by common MONDO mappings on source and on Wikidata

1 reference

Freebase Data Dumps

publication date

28 October 2013

GARD rare disease ID

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

Genetics Home Reference Conditions ID

0 references

1 reference

10 September 2022

https://golden.com/wiki/Vitiligo-6498P

Gran Enciclopèdia Catalana ID

0 references

Gran Enciclopèdia Catalana ID (former scheme)

0 references

Great Russian Encyclopedia Online ID (old version)

subject named as

ВИТИЛИГО

0 references

Human Phenotype Ontology ID

0 references

2 references

Disease Ontology

15 May 2019

Disease Ontology ID

Monarch Disease Ontology release 2018-06-29

28 July 2018

ICD-11 ID (Foundation)

0 references

ICD-11 ID (MMS)

ED63.0

subject named as

Vitiligo

0 references

1 reference

imported from Wikimedia project

Azerbaijani Wikipedia

Wikimedia import URL

https://az.wikipedia.org/?oldid=5783018

JSTOR topic ID (archived)

0 references

Microsoft Academic ID

0 references

0 references

0 references

NHS Health A to Z ID

0 references

OmegaWiki Defined Meaning

0 references

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

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

1 reference

http://www.patient.co.uk/patientplus/v.htm

1 reference

1 reference

imported from Wikimedia project

English Wikipedia

Wikimedia import URL

https://en.wikipedia.org/w/index.php?title=Vitiligo&oldid=953538473

0 references

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

2 references

Disease Ontology

15 May 2019

Disease Ontology ID

Human Phenotype Ontology release 2018-03-08

8 October 2018

Human Phenotype Ontology ID

UniProt disease ID

0 references

Vikidia article ID

0 references

WikiProjectMed ID

0 references

WikiSkripta article ID

0 references

WordNet 3.1 Synset ID

14256427-n

1 reference

subject named as

白癜风

0 references

Sitelinks

Wikipedia(78 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:Vitiligo

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