(Q504790)

English

nephrotic syndrome

Human disease

finnish congenital nephrosis
Nephrotic Syndrome
Nephrotic Syndromes
Syndrome, Nephrotic
Syndromes, Nephrotic
Nephrosis

In more languages

Statements

9 references

Disease Ontology release 2019-05-13

15 May 2019

Disease Ontology ID

[Familial nephrotic syndrome with focal glomerular sclerosis (author's transl)]

Modification of mineralocorticoid receptor function by Rac1 GTPase: implication in proteinuric kidney disease.

ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption.

DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN

The renal glomerulus of mice lacking s-laminin/laminin beta 2: nephrosis despite molecular compensation by laminin beta 1

Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible

Disruption of PTPRO causes childhood-onset nephrotic syndrome

Mutations in EMP2 cause childhood-onset nephrotic syndrome

0 references

1 reference

Disease Ontology release 2019-05-13

15 May 2019

Disease Ontology ID

Diabetic glomerulosclerosis (1) HE.jpg
700 × 527; 68 KB

1 reference

imported from Wikimedia project

Spanish Wikipedia

Wikimedia import URL

https://es.wikipedia.org/w/index.php?title=Síndrome_nefrótico&oldid=119928765

health specialty

0 references

drug 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

hydroflumethiazide

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

cyclophosphamide

1 reference

language of work or name

13 December 2016

methyclothiazide

1 reference

language of work or name

13 December 2016

1 reference

language of work or name

13 December 2016

hydrochlorothiazide

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

ethacrynic acid

1 reference

language of work or name

13 December 2016

bendroflumethiazide

1 reference

language of work or name

13 December 2016

1 reference

language of work or name

13 December 2016

trichlormethiazide

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

ethacrynate sodium

1 reference

language of work or name

13 December 2016

1 reference

Drug Indications Extracted from FAERS

2 October 2018

1 reference

Drug Indications Extracted from FAERS

2 October 2018

1 reference

Drug Indications Extracted from FAERS

2 October 2018

mycophenolate mofetil

1 reference

Drug Indications Extracted from FAERS

2 October 2018

1 reference

Drug Indications Extracted from FAERS

2 October 2018

methylprednisolone

1 reference

Drug Indications Extracted from FAERS

2 October 2018

1 reference

Drug Indications Extracted from FAERS

2 October 2018

2 October 1958

Food and Drug Administration

1 reference

Inxight: Drugs Database

2 November 2018

https://drugs.ncats.io/drug/77W477J15H

https://www.drugs.com/pro/diuril-injection.html

cyclophosphamide

12 April 1960

Food and Drug Administration

1 reference

Inxight: Drugs Database

2 November 2018

https://drugs.ncats.io/drug/6UXW23996M

http://www.accessdata.fda.gov/drugsatfda_docs/label/2013/012141s090,012142s112lbl.pdf

genetic association

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_1184&ncbiId=2262

http://www.genome.gov/gwastudies/index.cfm?gene=GPC5

Common variation in GPC5 is associated with acquired nephrotic syndrome

27 November 2019

1 reference

Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders

1 reference

ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption.

1 reference

ARHGDIA: a novel gene implicated in nephrotic syndrome

1 reference

DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN

1 reference

Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database

1 reference

NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome

1 reference

Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome

1 reference

Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible

1 reference

Disruption of PTPRO causes childhood-onset nephrotic syndrome

1 reference

Mutations in EMP2 cause childhood-onset nephrotic syndrome

described by source

Armenian Soviet Encyclopedia

0 references

581

2 references

Disease Ontology release 2019-05-13

15 May 2019

Disease Ontology ID

Monarch Disease Ontology release 2018-06-29sonu

4 August 2018

MONDO:0005377

581.9

1 reference

Monarch Disease Ontology release 2018-06-29sonu

4 August 2018

MONDO:0005377

NCI Thesaurus ID

C34845

1 reference

Disease Ontology release 2019-05-13

15 May 2019

Disease Ontology ID

C34845

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29sonu

4 August 2018

MONDO:0005377

http://purl.obolibrary.org/obo/DOID_1184

1 reference

Disease Ontology release 2019-05-13

15 May 2019

Disease Ontology ID

http://identifiers.org/doid/DOID:1184

1 reference

Identifiers.org Registry

http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233

http://purl.obolibrary.org/obo/HP_0000100

1 reference

Human Phenotype Ontology release 2018-03-08

8 October 2018

Human Phenotype Ontology ID

Identifiers

BNCF Thesaurus ID

1 reference

National Central Library of Florence

1 reference

imported from Wikimedia project

English Wikipedia

1 reference

imported from Wikimedia project

English Wikipedia

1 reference

imported from Wikimedia project

English Wikipedia

1 reference

imported from Wikimedia project

English Wikipedia

National Diet Library Auth ID

0 references

1 reference

Freebase Data Dumps

publication date

28 October 2013

Disease Ontology ID

1 reference

Disease Ontology release 2019-05-13

15 May 2019

Disease Ontology ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29sonu

4 August 2018

MONDO:0005377

2 references

Disease Ontology release 2019-05-13

15 May 2019

Disease Ontology ID

Human Phenotype Ontology release 2018-03-08

8 October 2018

Human Phenotype Ontology ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29sonu

4 August 2018

MONDO:0005377

Nephrotic-Syndrome

1 reference

nephrotic-syndrome

0 references

0 references

2 references

Disease Ontology release 2019-05-13

15 May 2019

Disease Ontology ID

Monarch Disease Ontology release 2018-06-29sonu

4 August 2018

MONDO:0005377

Encyclopædia Britannica Online ID

science/nephrotic-syndrome

0 references

0 references

MeSH descriptor ID

mapping relation type

Nephrotic Syndrome

1 reference

Monarch Disease Ontology release 2018-06-29sonu

4 August 2018

MONDO:0005377

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29sonu

4 August 2018

MONDO:0005377

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29sonu

4 August 2018

MONDO:0005377

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29sonu

4 August 2018

MONDO:0005377

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29sonu

4 August 2018

MONDO:0005377

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29sonu

4 August 2018

MONDO:0005377

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29sonu

4 August 2018

MONDO:0005377

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29sonu

4 August 2018

MONDO:0005377

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29sonu

4 August 2018

MONDO:0005377

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29sonu

4 August 2018

MONDO:0005377

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29sonu

4 August 2018

MONDO:0005377

MONDO:0005377

1 reference

Monarch Disease Ontology release 2018-06-29sonu

4 August 2018

MONDO:0005377

C12.777.419.630.643

0 references

C13.351.968.419.630.643

0 references

Human Phenotype Ontology ID

1 reference

Human Phenotype Ontology release 2018-03-08

8 October 2018

Human Phenotype Ontology ID

Sitelinks

Wikipedia(40 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Other sites(0 entries)

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