congenital diaphragmatic hernia (Q2163245): Difference between revisions

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Created claim: NL CR AUT ID (P691): ph1141968
Added qualifier: subject named as (P1810): vrozená brániční kýla, add qualifier value named_as to NKC AUT ID (P691) (details)
Property / NL CR AUT ID: ph1141968 / qualifier
 
subject named as: vrozená brániční kýla

Revision as of 11:43, 10 December 2022

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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