preeklampsi (Q61335)

Disease Ontology ^İngilizce

30 Kasım 2020

0 kaynak

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Hypertrophic decidual vasculopathy high mag.jpg
4.272 × 2.848; 6,07 MB

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ADRA1D ^İngilizce

TAS ^İngilizce

1 kaynak

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10591&ncbiId=146

http://www.genome.gov/gwastudies/index.cfm?gene=ADRA1D

Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort ^İngilizce

Phenocarta ^İngilizce

25 Mayıs 2020

INVS ^İngilizce

TAS ^İngilizce

1 kaynak

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10591&ncbiId=27130

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

Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort ^İngilizce

Phenocarta ^İngilizce

25 Mayıs 2020

ERP44 ^İngilizce

TAS ^İngilizce

1 kaynak

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10591&ncbiId=23071

http://www.genome.gov/gwastudies/index.cfm?gene=ERP44

Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort ^İngilizce

Phenocarta ^İngilizce

25 Mayıs 2020

FGF14 ^İngilizce

TAS ^İngilizce

1 kaynak

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10591&ncbiId=2259

http://www.genome.gov/gwastudies/index.cfm?gene=FGF14

Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort ^İngilizce

Phenocarta ^İngilizce

25 Mayıs 2020

MYCBP2 ^İngilizce

TAS ^İngilizce

1 kaynak

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10591&ncbiId=23077

http://www.genome.gov/gwastudies/index.cfm?gene=MYCBP2

Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort ^İngilizce

Phenocarta ^İngilizce

25 Mayıs 2020

TGFBRAP1 ^İngilizce

TAS ^İngilizce

1 kaynak

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10591&ncbiId=9392

http://www.genome.gov/gwastudies/index.cfm?gene=TGFBRAP1

Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort ^İngilizce

Phenocarta ^İngilizce

25 Mayıs 2020

WWTR1 ^İngilizce

TAS ^İngilizce

1 kaynak

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10591&ncbiId=25937

http://www.genome.gov/gwastudies/index.cfm?gene=WWTR1

Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort ^İngilizce

Phenocarta ^İngilizce

25 Mayıs 2020

MCM8 ^İngilizce

TAS ^İngilizce

1 kaynak

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10591&ncbiId=84515

http://www.genome.gov/gwastudies/index.cfm?gene=MCM8

Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort ^İngilizce

Phenocarta ^İngilizce

25 Mayıs 2020

STOX1 ^İngilizce

1 kaynak

Maternal segregation of the Dutch preeclampsia locus at 10q22 with a new member of the winged helix gene family ^İngilizce

FGFR2 ^İngilizce

1 kaynak

Wikimedia projeleri odak listesi

Bent bone dysplasia-FGFR2 type, a distinct skeletal disorder, has deficient canonical FGF signaling ^İngilizce

Vikiproje:Tıp

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gender gap on Dutch Wikipedia ^İngilizce

0 kaynak

Uluslararası Birinci Basamak Sağlık Sınıflandırması tanımlayıcı

W81

0 kaynak

NCI Thesaurus kimliği

C34943

1 kaynak

Disease Ontology ^İngilizce

15 Mayıs 2019

C85021

1 kaynak

Disease Ontology ^İngilizce

15 Mayıs 2019

http://purl.obolibrary.org/obo/DOID_10591

tam eşleşimi

1 kaynak

Disease Ontology ^İngilizce

30 Kasım 2020

http://identifiers.org/doid/DOID:10591

1 kaynak

Identifiers.org ^İngilizce

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

http://purl.obolibrary.org/obo/HP_0100602

1 kaynak

Human Phenotype Ontology release 2018-03-08 ^İngilizce

İnsan Fenotip Ontolojisi kimliği

8 Ekim 2018

HP:0100602

http://www.orpha.net/ORDO/Orphanet_275555

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Commons kategorisi

Pre-eclampsia

0 kaynak

Tanımlayıcılar

FAST kimliği

1075044

1 kaynak

İsrail Ulusal Kütüphanesi J9U kimliği

Faceted Application of Subject Terminology ^İngilizce

987007532094805171

1 kaynak

İsrail Ulusal Kütüphanesi

ABD Kongre Kütüphanesi yetki kimliği

sh91004039

1 kaynak

https://github.com/JohnMarkOckerbloom/ftl/blob/master/data/wikimap

3 Nisan 2019

preeklampsie

0 kaynak

MeSH tamımlayıcı kimliği

D011225

isimlendirilmesi

Pre-Eclampsia

scope note ^İngilizce

A complication of pregnancy, characterized by a complex of symptoms including maternal hypertension and proteinuria with or without pathological edema. Symptoms may range between mild and severe. Pre-eclampsia usually occurs after the 20th week of gestation, but may develop before this time in the presence of trophoblastic disease. (İngilizce)

2 kaynak

Disease Ontology ^İngilizce

15 Mayıs 2019

Human Phenotype Ontology release 2018-03-08 ^İngilizce