congenital diaphragmatic hernia (Q2163245): Difference between revisions

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Created claim: KEGG ID (P665): H01241
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Property / instance of
 
Property / instance of: disease / rank
Normal rank
 
Property / instance of: disease / reference
stated in: Disease Ontology
retrieved: 15 May 2019
Timestamp+2019-05-15T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Disease Ontology ID: DOID:3827
 
Property / instance of: disease / reference
 

Revision as of 13:46, 22 November 2020

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

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