congenital diaphragmatic hernia (Q16238): Difference between revisions

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Created claim: subclass of (P1): disease (Q5297)
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_2140
 
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Property / has effect
 
Property / has effect: asphyxia neonatorum / rank
 
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Property / afflicts
 
Property / afflicts: thoracic diaphragm / rank
 
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Property / health specialty
 
Property / health specialty: medical genetics / rank
 
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Property / health specialty
 
Property / health specialty: pediatrics / rank
 
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Property / exact match
 
Property / exact match: http://purl.obolibrary.org/obo/DOID_3827 / rank
 
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Property / exact match
 
Property / exact match: http://identifiers.org/doid/DOID:3827 / rank
 
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Property / exact match
 
Property / exact match: http://purl.obolibrary.org/obo/HP_0000776 / rank
 
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Property / exact match
 
Property / exact match: http://www.orpha.net/ORDO/Orphanet_2140 / rank
 
Normal rank

Latest revision as of 20:35, 21 December 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

Statements