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metabolic disease (Q2351083)

From Wikidata

disease that involving errors in metabolic processes of building or degradation of molecules

metabolic illness
disorder of metabolic process
metabolic disorder
metabolic diseases
disease of metabolism

Language	Label	Description	Also known as
default for all languages	No label defined
English	metabolic disease	disease that involving errors in metabolic processes of building or degradation of molecules	metabolic illness disorder of metabolic process metabolic disorder metabolic diseases disease of metabolism

Statements

class of disease

0 references

1 reference

Disease Ontology

25 November 2020

Disease Ontology ID

nutritional and metabolic diseases

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

Ragged red fibres - gtc - very high mag.jpg
3,642 × 2,428; 7.27 MB

1 reference

imported from Wikimedia project

Spanish Wikipedia

Wikimedia import URL

https://es.wikipedia.org/w/index.php?title=Trastorno_metabólico&oldid=120628296

0 references

health specialty

0 references

genetic association

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0014667&ncbiId=57818

http://www.genome.gov/gwastudies/index.cfm?gene=G6PC2

Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0014667&ncbiId=816

http://www.genome.gov/gwastudies/index.cfm?gene=CAMK2B

Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0014667&ncbiId=2590

http://www.genome.gov/gwastudies/index.cfm?gene=GALNT2

Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0014667&ncbiId=338

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

Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0014667&ncbiId=4023

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

Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0014667&ncbiId=19

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

Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0014667&ncbiId=10062

http://www.genome.gov/gwastudies/index.cfm?gene=NR1H3

Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0014667&ncbiId=23644

http://www.genome.gov/gwastudies/index.cfm?gene=EDC4

Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0014667&ncbiId=57223

http://www.genome.gov/gwastudies/index.cfm?gene=SMEK2

Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0014667&ncbiId=2646

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

Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0014667&ncbiId=51085

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

Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0014667&ncbiId=79068

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

Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0014667&ncbiId=84811

http://www.genome.gov/gwastudies/index.cfm?gene=BUD13

A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0014667&ncbiId=1071

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

A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0014667&ncbiId=8647

http://www.genome.gov/gwastudies/index.cfm?gene=ABCB11

A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0014667&ncbiId=7021

http://www.genome.gov/gwastudies/index.cfm?gene=TFAP2B

A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0014667&ncbiId=3992

http://www.genome.gov/gwastudies/index.cfm?gene=FADS1

A genome-wide association study of the metabolic syndrome in Indian Asian men

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0014667&ncbiId=9415

http://www.genome.gov/gwastudies/index.cfm?gene=FADS2

A genome-wide association study of the metabolic syndrome in Indian Asian men

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0014667&ncbiId=9815

http://www.genome.gov/gwastudies/index.cfm?gene=GIT2

A genome-wide association study of the metabolic syndrome in Indian Asian men

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0014667&ncbiId=9709

http://www.genome.gov/gwastudies/index.cfm?gene=HERPUD1

A genome-wide association study of the metabolic syndrome in Indian Asian men

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0014667&ncbiId=55118

http://www.genome.gov/gwastudies/index.cfm?gene=CRTAC1

A genome-wide association study of the metabolic syndrome in Indian Asian men

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0014667&ncbiId=6934

http://www.genome.gov/gwastudies/index.cfm?gene=TCF7L2

A genome-wide association study of the metabolic syndrome in Indian Asian men

25 May 2020

described by source

Encyclopædia Britannica 11th edition

statement is subject of

1911 Encyclopædia Britannica/Metabolic Diseases

0 references

on focus list of Wikimedia project

WikiProject Medicine

0 references

277.9

2 references

Disease Ontology

28 August 2019

Disease Ontology ID

Monarch Disease Ontology release 2018-06-29

28 July 2018

277.8

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

NCI Thesaurus ID

C3235

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

http://purl.obolibrary.org/obo/DOID_0014667

1 reference

Disease Ontology

25 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0014667

1 reference

Identifiers.org

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

Commons category

Metabolic diseases and disorders

0 references

topic's main category

Category:Metabolic disorders

0 references

Identifiers

1 reference

imported from Wikimedia project

German Wikipedia

Wikimedia import URL

https://de.wikipedia.org/w/index.php?title=Stoffwechselstörung&oldid=191655149

National Library of Israel J9U ID

987007565652605171

1 reference

National Library of Israel Names and Subjects Authority File

Library of Congress authority ID

subject named as

Metabolism--Disorders

1 reference

Integrated Authority File

National Library of Latvia ID

0 references

NDL Authority ID

subject named as

物質代謝異常

0 references

subject named as

metabolická onemocnění

0 references

subject named as

poruchy metabolismu

0 references

MeSH descriptor ID

mapping relation type

subject named as

Metabolic Diseases

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

broader concept

nutritional and metabolic diseases

0 references

ASC Leiden Thesaurus ID

0 references

Australian Educational Vocabulary ID

0 references

Disease Ontology ID

1 reference

Disease Ontology

25 November 2020

Disease Ontology ID

Encyclopædia Britannica Online ID

science/metabolic-disease

subject named as

metabolic disease

author name string

Gregory Enns

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

0 references

2 references

Disease Ontology

28 August 2019

Disease Ontology ID

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

ICD-11 ID (Foundation)

0 references

ICD-11 ID (MMS)

(5C50-5D2Z)

subject named as

Metabolic disorders

0 references

Postprocedural endocrine or metabolic disorders (5D40-5D46)

0 references

JSTOR topic ID (archived)

metabolic-disorders

0 references

Krugosvet article (archived)

medicina/OBMENA_VESHCHESTV_NARUSHENIYA.html

0 references

Microsoft Academic ID (discontinued)

0 references

0 references

museum-digital tag ID

0 references

0 references

National Historical Museums of Sweden ID

term/ff086bfa-7a71-4c22-a955-39eb0ef3ad7d

0 references

1 reference

26 January 2022

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

1 reference

26 January 2022

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

1 reference

26 January 2022

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

Store medisinske leksikon ID

stoffskiftesykdommer

mapping relation type

subject named as

stoffskiftesykdommer

0 references

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

concept/52165a02-988a-46a5-af0e-977f231f8468

0 references

subject named as

aineenvaihduntahäiriöt

ämnesomsättningsrubbningar

metabolic disorders

1 reference

YSO-Wikidata mapping project

27 December 2021

subject named as

代谢病

0 references

Sitelinks

Wikipedia(27 entries)

Wikibooks(1 entry)

jawikibooks 病理学/代謝障害

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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