nefropatia ^italian (Q1054718)

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patologia che colpisce il rene ^italian

Łéngua	Targheta	Descrision	Anca conosesto cofà
vèneto	nefropatia	Njiancora ła xé sta definìa na descrision
ingleze	kidney disease	urinary system disease that is located in the kidney	renal disease kidney damage kidney injury nephropathy disease of kidney disorder of kidney kidney necrosis nephron damage kidney diseases

Declaramenti

problema fìzego

0 riferimenti

classe di malattia ^italian

0 riferimenti

urinary system disease ^ingleze

1 riferimento

Disease Ontology ^italian

data de consultasion

30 nov 2020

ID Disease Ontology

organ-specific disease ^ingleze

0 riferimenti

0 riferimenti

specializzazione sanitaria ^italian

0 riferimenti

0 riferimenti

farmaco utilizzato per il trattamento ^italian

dopamina ^italian

1 riferimento

NDF-RT ^italian

identificativo NDF-RT ^italian

łéngua de l'òpara o del nòme

data de consultasion

13 dis 2016

paricalcitol ^ingleze

1 riferimento

Drug Indications Extracted from FAERS ^ingleze

data de consultasion

2 oto 2018

localizzazione anatomica ^italian

1 riferimento

Disease Ontology ^italian

data de consultasion

15 maj 2019

ID Disease Ontology

associazione genetica ^italian

SLC13A3 ^italian

mètodo de determenasion

studio di associazione genome-wide ^italian

TAS ^italian

1 riferimento

URL de refarensa

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_557&ncbiId=64849

http://www.genome.gov/gwastudies/index.cfm?gene=SLC13A3

Phenocarta ^ingleze

An integrative study of the genetic, social and environmental determinants of chronic kidney disease characterized by tubulointerstitial damages in the North Central Region of Sri Lanka ^ingleze

data de consultasion

25 maj 2020

UMOD ^italian

mètodo de determenasion

studio di associazione genome-wide ^italian

TAS ^italian

1 riferimento

URL de refarensa

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_557&ncbiId=7369

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

Phenocarta ^ingleze

Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases ^ingleze

data de consultasion

25 maj 2020

TFDP2 ^italian

mètodo de determenasion

studio di associazione genome-wide ^italian

TAS ^italian

1 riferimento

URL de refarensa

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_557&ncbiId=7029

http://www.genome.gov/gwastudies/index.cfm?gene=TFDP2

Phenocarta ^ingleze

New loci associated with kidney function and chronic kidney disease ^ingleze

data de consultasion

25 maj 2020

PRKAG2 ^ingleze

mètodo de determenasion

studio di associazione genome-wide ^italian

TAS ^italian

1 riferimento

URL de refarensa

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_557&ncbiId=51422

http://www.genome.gov/gwastudies/index.cfm?gene=PRKAG2

Phenocarta ^ingleze

New loci associated with kidney function and chronic kidney disease ^ingleze

data de consultasion

25 maj 2020

ATXN2 ^italian

mètodo de determenasion

studio di associazione genome-wide ^italian

TAS ^italian

1 riferimento

URL de refarensa

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_557&ncbiId=6311

http://www.genome.gov/gwastudies/index.cfm?gene=ATXN2

Phenocarta ^ingleze

New loci associated with kidney function and chronic kidney disease ^ingleze

data de consultasion

25 maj 2020

DACH1 ^italian

mètodo de determenasion

studio di associazione genome-wide ^italian

TAS ^italian

1 riferimento

URL de refarensa

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_557&ncbiId=1602

http://www.genome.gov/gwastudies/index.cfm?gene=DACH1

Phenocarta ^ingleze

New loci associated with kidney function and chronic kidney disease ^ingleze

data de consultasion

25 maj 2020

CPS1 ^italian

mètodo de determenasion

studio di associazione genome-wide ^italian

TAS ^italian

1 riferimento

URL de refarensa

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_557&ncbiId=1373

http://www.genome.gov/gwastudies/index.cfm?gene=CPS1

Phenocarta ^ingleze

New loci associated with kidney function and chronic kidney disease ^ingleze

data de consultasion

25 maj 2020

SLC22A2 ^italian

mètodo de determenasion

studio di associazione genome-wide ^italian

TAS ^italian

1 riferimento

URL de refarensa

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_557&ncbiId=6582

http://www.genome.gov/gwastudies/index.cfm?gene=SLC22A2

Phenocarta ^ingleze

New loci associated with kidney function and chronic kidney disease ^ingleze

data de consultasion

25 maj 2020

WDR37 ^italian

mètodo de determenasion

studio di associazione genome-wide ^italian

TAS ^italian

1 riferimento

URL de refarensa

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_557&ncbiId=22884

http://www.genome.gov/gwastudies/index.cfm?gene=WDR37

Phenocarta ^ingleze

New loci associated with kidney function and chronic kidney disease ^ingleze

data de consultasion

25 maj 2020

WDR72 ^italian

mètodo de determenasion

studio di associazione genome-wide ^italian

TAS ^italian

1 riferimento

URL de refarensa

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_557&ncbiId=256764

http://www.genome.gov/gwastudies/index.cfm?gene=WDR72

Phenocarta ^ingleze

New loci associated with kidney function and chronic kidney disease ^ingleze

data de consultasion

25 maj 2020

SHROOM3 ^italian

mètodo de determenasion

studio di associazione genome-wide ^italian

TAS ^italian

1 riferimento

URL de refarensa

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_557&ncbiId=57619

http://www.genome.gov/gwastudies/index.cfm?gene=SHROOM3

Phenocarta ^ingleze

Multiple loci associated with indices of renal function and chronic kidney disease ^ingleze

data de consultasion

25 maj 2020

PVT1 ^italian

mètodo de determenasion

studio di associazione genome-wide ^italian

TAS ^italian

1 riferimento

URL de refarensa

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_557&ncbiId=5820

http://www.genome.gov/gwastudies/index.cfm?gene=PVT1

Phenocarta ^ingleze

Identification of PVT1 as a candidate gene for end-stage renal disease in type 2 diabetes using a pooling-based genome-wide single nucleotide polymorphism association study ^ingleze

data de consultasion

25 maj 2020

PKD1 ^italian

1 riferimento

Open Targets Platform ^ingleze

data de consultasion

24 ago 2023

URL de refarensa

https://platform.opentargets.org/evidence/ENSG00000008710/EFO_0003086

determinà da l'eurìstega

inferred from an Open Targets association score over 0.7 ^ingleze

descrivesto drento de ła fonte

Encyclopædia Britannica Eleventh Edition

afirmasion detajada de

1911 Encyclopædia Britannica/Kidney Diseases ^ingleze

0 riferimenti

lista de intaresi par el projeto Wikimèdia

Progetto:Medicina ^italian

0 riferimenti

583.81

1 riferimento

Monarch Disease Ontology release 2018-06-29 ^ingleze

data de consultasion

28 luj 2018

ID NCI Thesaurus

C34843

1 riferimento

Disease Ontology ^italian

data de consultasion

15 maj 2019

ID Disease Ontology

C3149

1 riferimento

Disease Ontology ^italian

data de consultasion

15 maj 2019

ID Disease Ontology

corispondensa justa

http://purl.obolibrary.org/obo/DOID_557

1 riferimento

Disease Ontology ^italian

data de consultasion

30 nov 2020

ID Disease Ontology

http://identifiers.org/doid/DOID:557

1 riferimento

registro identifiers.org ^italian

URL de refarensa

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

http://purl.obolibrary.org/obo/HP_0000077

1 riferimento

Human Phenotype Ontology release 2018-03-08 ^ingleze

data de consultasion

8 oto 2018

ID Human Phenotype Ontology

http://purl.obolibrary.org/obo/HP_0000112

1 riferimento

Human Phenotype Ontology release 2018-03-08 ^ingleze

data de consultasion

8 oto 2018

ID Human Phenotype Ontology

neuropatia periferica ^italian

1 riferimento

Wikipedia in inglese

URL inportà da Wikimèdia

https://en.wikipedia.org/w/index.php?title=Kidney_disease&oldid=950239265

categoria Commons

Kidney diseases

1 riferimento

Wikipedia in inglese

categoria prinsipałe

Category:Kidney diseases ^ingleze

1 riferimento

Wikipedia in ucraino ^italian

1 riferimento

Identifegadori

Rein -- Maladies

1 riferimento

Nuovo soggettario ^italian

URL de refarensa

https://thes.bncf.firenze.sbn.it/termine.php?id=44109

data de consultasion

16 xug 2021

1 riferimento

Wikipedia in tedesco ^italian

ID J9U Biblioteca Nasionałe de Israełe

987007543429505171

1 riferimento

National Library of Israel Names and Subjects Authority File ^ingleze

Kidneys--Diseases

1 riferimento

Gemeinsame Normdatei

nefropatie

0 riferimenti

nemoci ledvin

0 riferimenti

identificativo AGROVOC ^italian

0 riferimenti

tipo de rełasion

corrispondenza esatta ^italian

Kidney Diseases

1 riferimento

Monarch Disease Ontology release 2018-06-29 ^ingleze

data de consultasion

28 luj 2018

C12.050.351.968.419

0 riferimenti

C12.200.777.419

0 riferimenti

0 riferimenti

ID Analysis & Policy Observatory de tèrmani

0 riferimenti

1 riferimento

BabelNet ^italian

Baidu Tieba name ^ingleze

nùmaro de òpare

150 893

26 mar 2023

0 riferimenti

Nefrite

0 riferimenti

ID Disease Ontology

1 riferimento

Disease Ontology ^italian

data de consultasion

30 nov 2020

ID Disease Ontology

0 riferimenti

0 riferimenti

Experimental Factor Ontology ID ^ingleze

1 riferimento

determinà da l'eurìstega

inferred by common MONDO mappings on source and on Wikidata ^ingleze

1 riferimento

Freebase Data Dumps ^italian

data de publicasion

28 oto 2013

identificativo Gran Enciclopèdia Catalana ^italian

0 riferimenti

ID Gran Enciclopèdia Catalana

0 riferimenti

ID Granda Ençiclopedia Rusa in lìnea

НЕФРОПАТИЯ

0 riferimenti

ID Human Phenotype Ontology

1 riferimento

Human Phenotype Ontology release 2018-03-08 ^ingleze

data de consultasion

8 oto 2018

ID Human Phenotype Ontology

1 riferimento

Human Phenotype Ontology release 2018-03-08 ^ingleze

data de consultasion

8 oto 2018

ID Human Phenotype Ontology

2 riferimenti

Disease Ontology ^italian

data de consultasion

15 maj 2019

ID Disease Ontology

Monarch Disease Ontology release 2018-06-29 ^ingleze

data de consultasion

28 luj 2018

2 riferimenti

Disease Ontology ^italian

data de consultasion

15 maj 2019

ID Disease Ontology

Monarch Disease Ontology release 2018-06-29 ^ingleze

data de consultasion

28 luj 2018

0 riferimenti

ID JSTOR de ojeto

kidney-diseases

0 riferimenti

1 riferimento

KBpedia ^italian

data de consultasion

9 luj 2020

ID Microsoft Academic

0 riferimenti

0 riferimenti

identificativo NALT ^italian

0 riferimenti

0 riferimenti

identificativo Internetowa encyklopedia PWN ^italian

0 riferimenti

identificativo OpenAlex ^italian

1 riferimento

OpenAlex ^italian

data de consultasion

26 zen 2022

URL de refarensa

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

URL del archìvio

https://web.archive.org/web/20220125070108/https://docs.openalex.org/download-snapshot/snapshot-data-format

data de archiviasion

25 zen 2022

1 riferimento

OpenAlex ^italian

data de consultasion

26 zen 2022

URL de refarensa

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

1 riferimento

OpenAlex ^italian

data de consultasion

26 zen 2022

URL de refarensa

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

1 riferimento

OpenAlex ^italian

data de consultasion

26 zen 2022

URL de refarensa

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

0 riferimenti

ID Quora de on sojeto

1 riferimento

ID Store medisinske leksikon

0 riferimenti

ID UK Parliament thesaurus

Kidney diseases

0 riferimenti

3 riferimenti

Disease Ontology ^italian

data de consultasion

15 maj 2019

ID Disease Ontology

Human Phenotype Ontology release 2018-03-08 ^ingleze

data de consultasion

8 oto 2018

ID Human Phenotype Ontology

Human Phenotype Ontology release 2018-03-08 ^ingleze

data de consultasion

8 oto 2018

ID Human Phenotype Ontology

1 riferimento

Human Phenotype Ontology release 2018-03-08 ^ingleze

data de consultasion

8 oto 2018

ID Human Phenotype Ontology

1 riferimento

Human Phenotype Ontology release 2018-03-08 ^ingleze

data de consultasion

8 oto 2018

ID Human Phenotype Ontology

1 riferimento

determinà da l'eurìstega

inferred by common Orphanet mappings on source and on Wikidata ^ingleze

UMLS 2023 ^ingleze

data de consultasion

16 xug 2023

1 riferimento

YSO-Wikidata mapping project ^ingleze

data de consultasion

24 nov 2021

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Wikipedia(34 siti)

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