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(Q16238)

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Statements

instance of
designated intractable/rare diseases
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developmental defect during embryogenesis
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rare disease
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class of disease
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subclass of
diaphragm disease
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diaphragmatic hernia
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congenital disorder
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rare genetic developmental defect during embryogenesis
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rare genetic respiratory disease
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disease
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has effect
asphyxia neonatorum
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afflicts
thoracic diaphragm
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health specialty
medical genetics
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pediatrics
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exact match
http://purl.obolibrary.org/obo/DOID_3827
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http://identifiers.org/doid/DOID:3827
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http://purl.obolibrary.org/obo/HP_0000776
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http://www.orpha.net/ORDO/Orphanet_2140
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Sitelinks

⧼wikibase-sitelinks-mywikigroup⧽(0 entries)

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    Retrieved from "https://wiki.tiffa.net/w/index.php?title=Item:Q16238&oldid=84984"
    Last edited on 21 December 2023, at 20:35

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        • This page was last edited on 21 December 2023, at 20:35.
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