congenital diaphragmatic hernia (Q2163245): Difference between revisions

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Changed label, description and/or aliases in he
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Removed claim: WikiProjectMed ID (P11143): Congenital diaphragmatic hernia, дублирующееся значение / duplicate value
Tag: Manual revert
 
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label / cslabel / cs
 
vrozená brániční kýla
label / uklabel / uk
 
вроджена діафрагмальна грижа
label / sllabel / sl
 
prirojena diafragmalna kila
description / ukdescription / uk
 
хвороба
Property / subclass of: rare genetic developmental defect during embryogenesis / 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_0009103
Property / subclass of: rare genetic developmental defect during embryogenesis / 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:0009103
 
Property / subclass of: rare genetic respiratory 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_0009103
Property / subclass of: rare genetic respiratory 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:0009103
 
Property / UMLS CUIProperty / UMLS CUI
Property / UMLS CUI: C0235833 / reference
 
stated in: Human Phenotype Ontology release 2018-03-08
retrieved: 8 October 2018
Timestamp+2018-10-08T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Human Phenotype Ontology ID: HP:0000776
Property / UMLS CUI: C1857284 / 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_0009103
Property / UMLS CUI: C1857284 / 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:0009103
 
Property / UMLS CUI
 
Property / UMLS CUI: C0235833 / rank
Normal rank
 
Property / UMLS CUI: C0235833 / reference
stated in: Human Phenotype Ontology release 2018-03-08
retrieved: 8 October 2018
Timestamp+2018-10-08T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Human Phenotype Ontology ID: HP:0000776
 
Property / instance of: developmental defect during embryogenesis / 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_0009103
Property / instance of: developmental defect during embryogenesis / 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:0009103
 
Property / Mondo ID
 
Property / Mondo ID: MONDO:0009103 / rank
Normal rank
 
Property / Mondo ID: MONDO:0009103 / 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:0009103
 
Property / MeSH tree codeProperty / MeSH tree code
Property / subclass of
 
Property / subclass of: disease / rank
 
Normal rank
Property / UMLS CUI
 
Property / UMLS CUI: C0265699 / rank
 
Normal rank
Property / UMLS CUI: C0265699 / reference
 
based on heuristic: inferred by common MeSH mappings on source and on Wikidata
stated in: UMLS 2023
retrieved: 25 May 2023
Timestamp+2023-05-25T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / instance of
 
Property / instance of: class of disease / rank
 
Normal rank
Property / NL CR AUT ID
 
Property / NL CR AUT ID: ph1141968 / rank
 
Normal rank
Property / NL CR AUT ID: ph1141968 / qualifier
 
subject named as: vrozená brániční kýla
Property / PatientsLikeMe condition ID
 
Property / PatientsLikeMe condition ID: congenital-diaphragmatic-hernia / rank
 
Normal rank
Property / Experimental Factor Ontology ID
 
Property / Experimental Factor Ontology ID: 0007216 / rank
 
Normal rank
Property / Experimental Factor Ontology ID: 0007216 / reference
 
Property / WikiProjectMed ID
 
Property / WikiProjectMed ID: Congenital diaphragmatic hernia / rank
 
Normal rank
Property / Mondo ID
 
Property / Mondo ID: MONDO_0009103 / rank
 
Normal rank

Latest revision as of 07:56, 15 June 2024

diaphragm disease characterized by the lack of development of all or part of the diaphragm, which results in an abnormal opening that allows the stomach and intestines to move into the chest cavity and crowd the heart and lungs
  • diaphragmatic hernia
  • congenital diaphragmatic hernias
  • DIAPHRAGMATIC HERNIA 2
  • DIAPHRAGMATIC HERNIA 2; DIH2
  • Hernias, Diaphragmatic, Congenital
Language Label Description Also known as
English
congenital diaphragmatic hernia
diaphragm disease characterized by the lack of development of all or part of the diaphragm, which results in an abnormal opening that allows the stomach and intestines to move into the chest cavity and crowd the heart and lungs
  • diaphragmatic hernia
  • congenital diaphragmatic hernias
  • DIAPHRAGMATIC HERNIA 2
  • DIAPHRAGMATIC HERNIA 2; DIH2
  • Hernias, Diaphragmatic, Congenital

Statements

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Congenital diaphragmatic hernia

Identifiers

vrozená brániční kýla
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LB00.0
Congenital diaphragmatic hernia
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Congenital diaphragmatic hernia
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