congenital diaphragmatic hernia (Q16238): Difference between revisions
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Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_2140 |
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| Property / subclass of | |||
| Property / subclass of: rare genetic respiratory disease / rank | |||
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| Property / subclass of: disease / rank | |||
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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: 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 | |||
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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 |
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