Wolff–Parkinson–White syndrome (Q925092): Difference between revisions
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Created claim: OpenAlex ID (P10283): C2909624804, batch #74838 |
Changed Russian label: синдром Вольфа — Паркинсона — Уайта |
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(45 intermediate revisions by 21 users not shown) | |||||||||||||||
label / en | label / en | ||||||||||||||
Wolff–Parkinson–White syndrome | |||||||||||||||
label / es | label / es | ||||||||||||||
síndrome de Wolff-Parkinson-White | |||||||||||||||
label / pt | label / pt | ||||||||||||||
síndrome de Wolff-Parkinson-White | |||||||||||||||
label / ru | label / ru | ||||||||||||||
синдром Вольфа — Паркинсона — Уайта | |||||||||||||||
label / ca | label / ca | ||||||||||||||
síndrome de Wolff-Parkinson-White | |||||||||||||||
label / uz | label / uz | ||||||||||||||
Wolff-Parkinson-White sindromi | |||||||||||||||
label / sr | label / sr | ||||||||||||||
Волф-Паркинсон-Вајт синдром | |||||||||||||||
label / pt-br | label / pt-br | ||||||||||||||
síndrome de Wolff-Parkinson-White | |||||||||||||||
aliases / en / 0 | aliases / en / 0 | ||||||||||||||
WPWS | |||||||||||||||
aliases / en / 1 | aliases / en / 1 | ||||||||||||||
Wolff-Parkinson-White syndrome | |||||||||||||||
aliases / ca / 0 | aliases / ca / 0 | ||||||||||||||
síndrome de preexcitació | |||||||||||||||
aliases / ca / 1 | aliases / ca / 1 | ||||||||||||||
aliases / pt-br / 0 | aliases / pt-br / 0 | ||||||||||||||
SWPW | |||||||||||||||
description / ko | description / ko | ||||||||||||||
심장 전기 전도계가 빠르게 흥분하는 질환 | |||||||||||||||
description / ca | description / ca | ||||||||||||||
anomalia congènita cardíaca | |||||||||||||||
description / pt-br | description / pt-br | ||||||||||||||
síndrome congênita que resulta da presença de vias elétricas adicionais no sistema de condução elétrica do coração | |||||||||||||||
description / uk | description / uk | ||||||||||||||
хвороба | |||||||||||||||
Property / subclass of: genetic disease / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0008685 | |||||||||||||||
Property / subclass of: genetic disease / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0008685 | |||||||||||||||
Property / NCI Thesaurus ID: C35132 / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0008685 | |||||||||||||||
Property / NCI Thesaurus ID: C35132 / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0008685 | |||||||||||||||
Property / UMLS CUI: C0264897 / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0008685 | |||||||||||||||
Property / UMLS CUI: C0264897 / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0008685 | |||||||||||||||
Property / UMLS CUI: C0032915 / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0008685 | |||||||||||||||
Property / UMLS CUI: C0032915 / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0008685 | |||||||||||||||
Property / ICD-10-CM: I45.6 / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0008685 | |||||||||||||||
Property / ICD-10-CM: I45.6 / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0008685 | |||||||||||||||
Property / MeSH descriptor ID: D014927 / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0008685 | |||||||||||||||
Property / MeSH descriptor ID: D014927 / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0008685 | |||||||||||||||
Property / ICD-9-CM: 426.7 / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0008685 | |||||||||||||||
Property / ICD-9-CM: 426.7 / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0008685 | |||||||||||||||
Property / Mondo ID | |||||||||||||||
Property / Mondo ID: MONDO:0008685 / rank | |||||||||||||||
Property / Mondo ID: MONDO:0008685 / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0008685 | |||||||||||||||
Property / Human Phenotype Ontology ID: HP:0001716 / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0008685 | |||||||||||||||
Property / Human Phenotype Ontology ID: HP:0001716 / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0008685 | |||||||||||||||
Property / Orphanet ID: 907 / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0008685 | |||||||||||||||
Property / Orphanet ID: 907 / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0008685 | |||||||||||||||
Property / genetic association: PRKAG2 / reference | |||||||||||||||
stated in: Open Targets Platform retrieved: 24 August 2023
reference URL: https://platform.opentargets.org/evidence/ENSG00000106617/EFO_1001450 based on heuristic: inferred from an Open Targets association score over 0.7 | |||||||||||||||
Property / OpenAlex ID: C2909624804 / reference | |||||||||||||||
stated in: OpenAlex retrieved: 26 January 2022
reference URL: https://docs.openalex.org/download-snapshot/snapshot-data-format | |||||||||||||||
Property / subclass of | |||||||||||||||
Property / subclass of: disease / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / instance of | |||||||||||||||
Property / instance of: class of disease / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / WikiProjectMed ID | |||||||||||||||
Property / WikiProjectMed ID: Wolff–Parkinson–White syndrome / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / PatientsLikeMe condition ID | |||||||||||||||
Property / PatientsLikeMe condition ID: wolff-parkinson-white / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / Experimental Factor Ontology ID | |||||||||||||||
Property / Experimental Factor Ontology ID: 1001450 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / Experimental Factor Ontology ID: 1001450 / reference | |||||||||||||||
Property / UniProt disease ID | |||||||||||||||
Property / UniProt disease ID: DI-01150 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Property / Mondo ID | |||||||||||||||
Property / Mondo ID: MONDO_0008685 / rank | |||||||||||||||
Normal rank | |||||||||||||||
links / elwiki / name | links / elwiki / name | ||||||||||||||
links / skwiki / name | links / skwiki / name | ||||||||||||||
links / uzwiki / name | links / uzwiki / name | ||||||||||||||
links / srwiki / name | links / srwiki / name | ||||||||||||||
Latest revision as of 23:31, 27 April 2024
disorder due to a specific type of problem with the electrical system of the heart which has resulted in symptoms
- Anomalous A-V excitation
- anomalous atrioventricular excitation
- WPW syndrome
- Wolff-Parkinson-White pattern (finding)
- WPW
- Wolff-Parkinson-White pattern
- Accessory Atrioventricular Pathways
- Preexcitation Syndrome
- WPWS
- Wolff-Parkinson-White syndrome
Language | Label | Description | Also known as |
---|---|---|---|
English | Wolff–Parkinson–White syndrome |
disorder due to a specific type of problem with the electrical system of the heart which has resulted in symptoms |
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Statements
1 reference
1 reference
DeltaWave09.JPG
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1,194 × 1,005; 770 KB
Ona delta típica de la Síndrome WPW. Interval PR curt. (Catalan)
0 references
1 reference
3 references
426.7
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C35132
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1 reference
1 reference
Wolff–Parkinson–White syndrome
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Identifiers
Syndrome de Wolff-Parkinson-White
1 reference
Wolff-Parkinson-White syndrome
1 reference
Wolff-Parkinson-White Syndrome
1 reference
1 reference
2 references
2 references
1 reference
1 reference
1 reference
1 reference
2 references
Sitelinks
Wikipedia(31 entries)
- arwiki متلازمة وولف -باركنسون -وايت
- cawiki Síndrome de Wolff-Parkinson-White
- dewiki Wolff-Parkinson-White-Syndrom
- elwiki Σύνδρομο Γουλφ-Πάρκινσον-Γουάιτ
- enwiki Wolff–Parkinson–White syndrome
- eswiki Síndrome de Wolff-Parkinson-White
- euwiki Wolff-Parkinson-White sindrome
- fawiki سندرم ولف پارکینسون وایت
- fiwiki Wolff–Parkinson–Whiten oireyhtymä
- frwiki Syndrome de Wolff-Parkinson-White
- glwiki Síndrome de Wolff-Parkinson-White
- hewiki תסמונת וולף–פרקינסון–וייט
- huwiki Wolff–Parkinson–White-szindróma
- hywiki Ուոլֆ–Պարկինսոն–Ուայթի համախտանիշ
- idwiki Sindrom Wolff–Parkinson–White
- itwiki Sindrome di Wolff-Parkinson-White
- jawiki ウォルフ・パーキンソン・ホワイト症候群
- kowiki 볼프 파킨슨 화이트 증후군
- nlwiki Syndroom van Wolff-Parkinson-White
- orwiki ଉଲ୍ଫ-ପାର୍କିନସନ-ହ୍ୱାଇଟ ସିଣ୍ଡ୍ରୋମ
- plwiki Zespół Wolffa-Parkinsona-White’a
- ptwiki Síndrome de Wolff-Parkinson-White
- ruwiki Синдром Вольфа — Паркинсона — Уайта
- simplewiki Wolff–Parkinson–White syndrome
- skwiki Wolffov-Parkinsonov-Whiteov syndróm
- slwiki Wolff-Parkinson-Whiteov sindrom
- srwiki Синдром преексцитације срчаних комора
- ukwiki Синдром Вольфа — Паркінсона — Вайта
- uzwiki Wolff-Parkinson-White sindromi
- viwiki Hội chứng Wolff–Parkinson–White
- zhwiki 沃夫巴金森懷特症候群
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:Wolff–Parkinson–White syndrome