Wolff–Parkinson–White syndrome (Q925092): Difference between revisions

From Wikidata
Jump to navigation Jump to search
Jordi escarre (talk | contribs)
Added [ca] description: anomalia congènita cardíaca
Tag: Wikidata user interface
Changed Russian label: синдром Вольфа — Паркинсона — Уайта
 
(28 intermediate revisions by 12 users not shown)
label / enlabel / en
Wolff-Parkinson-White syndrome
Wolff–Parkinson–White syndrome
label / rulabel / ru
Синдром Вольфа — Паркинсона — Уайта
синдром Вольфа — Паркинсона — Уайта
label / pt-brlabel / pt-br
 
síndrome de Wolff-Parkinson-White
aliases / en / 0aliases / en / 0
 
WPWS
aliases / en / 1aliases / en / 1
 
Wolff-Parkinson-White syndrome
aliases / pt-br / 0aliases / pt-br / 0
 
SWPW
description / pt-brdescription / pt-br
 
síndrome congênita que resulta da presença de vias elétricas adicionais no sistema de condução elétrica do coração
description / ukdescription / uk
 
хвороба
Property / subclass of: genetic disease / reference
 
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO_0008685
Property / subclass of: genetic disease / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0008685
 
Property / subclass of
 
Property / subclass of: disease of a particular individual / rank
Normal rank
 
Property / NCI Thesaurus ID: C35132 / reference
 
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO_0008685
Property / NCI Thesaurus ID: C35132 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0008685
 
Property / UMLS CUI: C0264897 / reference
 
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO_0008685
Property / UMLS CUI: C0264897 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0008685
 
Property / UMLS CUI: C0032915 / reference
 
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO_0008685
Property / UMLS CUI: C0032915 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0008685
 
Property / ICD-10-CM: I45.6 / reference
 
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO_0008685
Property / ICD-10-CM: I45.6 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0008685
 
Property / MeSH descriptor ID: D014927 / reference
 
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO_0008685
Property / MeSH descriptor ID: D014927 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0008685
 
Property / ICD-9-CM: 426.7 / reference
 
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO_0008685
Property / ICD-9-CM: 426.7 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0008685
 
Property / Mondo ID
 
Property / Mondo ID: MONDO:0008685 / rank
Normal rank
 
Property / Mondo ID: MONDO:0008685 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

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
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

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
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0008685
 
Property / Orphanet ID: 907 / reference
 
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO_0008685
Property / Orphanet ID: 907 / reference
stated in: Monarch Disease Ontology release 2018-06-29
retrieved: 28 July 2018
Timestamp+2018-07-28T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Mondo ID: MONDO:0008685
 
Property / genetic association: PRKAG2 / reference
 
Property / subclass of
 
Property / subclass of: disease / 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 / namelinks / elwiki / name
links / srwiki / namelinks / 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
  • 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

Statements

0 references
0 references
DeltaWave09.JPG
1,194 × 1,005; 770 KB
Ona delta típica de la Síndrome WPW. Interval PR curt. (Catalan)
0 references
0 references
0 references
0 references
Wolff–Parkinson–White syndrome
0 references

Identifiers

0 references
0 references
BC81.4
Wolff-Parkinson-White syndrome
0 references
0 references