congenital diaphragmatic hernia (Q2163245): Difference between revisions

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Created claim: PatientsLikeMe condition ID (P4233): congenital-diaphragmatic-hernia
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Property / Experimental Factor Ontology ID: 0007216 / rank
 
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Revision as of 17:41, 21 August 2023

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

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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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