congenital diaphragmatic hernia (Q2163245): Difference between revisions

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Changed reference of claim: subclass of (P279): rare genetic respiratory disease (Q55785522), см. / see autofix на / on Property talk:P5270
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
 

Revision as of 18:38, 25 February 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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