Item:Q16238: Difference between revisions
Created a new Item: 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 |
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_2140 |
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| Property / instance of: designated intractable/rare diseases / rank | |||
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| Property / instance of: developmental defect during embryogenesis / rank | |||
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| Property / instance of: rare disease / rank | |||
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| Property / instance of: class of disease / rank | |||
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| Property / subclass of: diaphragm disease / rank | |||
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| Property / subclass of: diaphragmatic hernia / rank | |||
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| Property / subclass of: congenital disorder / rank | |||
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| Property / subclass of: rare genetic developmental defect during embryogenesis / rank | |||
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| Property / subclass of: rare genetic respiratory disease / rank | |||
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| Property / subclass of: disease / rank | |||
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| Property / has effect: asphyxia neonatorum / rank | |||
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| Property / afflicts: thoracic diaphragm / rank | |||
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| Property / health specialty: medical genetics / rank | |||
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| Property / health specialty: pediatrics / rank | |||
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| Property / exact match: http://purl.obolibrary.org/obo/DOID_3827 / rank | |||
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| Property / exact match: http://identifiers.org/doid/DOID:3827 / rank | |||
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| 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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