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Acute renal failure with acute cortical necrosis
Acute respiratory failure
Chronic type 1 respiratory failure
Chronic type II respiratory failure
Hereditary myopathy with early respiratory failure
Respiratory failure

Translation of "acute respiratory failure " (English → French) :

TERMINOLOGY
see also In-Context Translations below
Acute respiratory failure
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insuffisance respiratoire aigüe
SNOMEDCT-BE (disorder) / 65710008
SNOMEDCT-BE (disorder) / 65710008
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https://browser.ihtsdotools.or (...) [HTML]
Acute respiratory failure
https://icd.who.int/browse10/2 (...) (...) [HTML]
Insuffisance respiratoire aiguë
WORLD HEALTH ORGANIZATION ICD-10: J96.0
WORLD HEALTH ORGANIZATION ICD-10: J96.0
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
This syndrome has features of fibuloulnar dysostosis with renal anomalies. It has been described in two siblings born to nonconsanguinous parents. The syndrome is lethal at birth (respiratory failure). Clinical manifestations include ear and facial a
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syndrome d'hypoplasie péroné-cubitus-anomalies rénales
SNOMEDCT-BE (respiratory failure). Clinical manifestations include ear and facial a / 716094008
SNOMEDCT-BE (disorder) / 716094008
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https://browser.ihtsdotools.or (...) [HTML]
A rare genetic parenchymal hepatic disease with characteristics of acute liver failure that occurs in the first year of life, which manifests with failure to thrive, hypotonia, moderate global developmental delay, seizures, abnormal liver function te
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syndrome d'insuffisance hépatique aigüe infantile-manifestations multisystémiques
SNOMEDCT-BE (disorder) / 774207004
SNOMEDCT-BE (disorder) / 774207004
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https://browser.ihtsdotools.or (...) [HTML]
Acute renal failure with acute cortical necrosis
https://icd.who.int/browse10/2 (...) (...) [HTML]
Insuffisance rénale aiguë avec nécrose corticale aiguë
WORLD HEALTH ORGANIZATION ICD-10: N17.1
WORLD HEALTH ORGANIZATION ICD-10: N17.1
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
Chronic type 1 respiratory failure
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insuffisance respiratoire hypoxémique chronique
SNOMEDCT-BE (disorder) / 428173007
SNOMEDCT-BE (disorder) / 428173007
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Hereditary myopathy with early respiratory failure
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myopathie héréditaire avec atteinte respiratoire précoce
SNOMEDCT-BE (disorder) / 702373006
SNOMEDCT-BE (disorder) / 702373006
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https://browser.ihtsdotools.or (...) [HTML]
Chronic type II respiratory failure
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insuffisance respiratoire hypercapnique chronique
SNOMEDCT-BE (disorder) / 426896000
SNOMEDCT-BE (disorder) / 426896000
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Respiratory failure
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insuffisance respiratoire
SNOMEDCT-BE (disorder) / 409622000
SNOMEDCT-BE (disorder) / 409622000
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
A rare genetic motor neuron disease with characteristics of progressive early respiratory failure associated with diaphragm paralysis, distal muscular weakness, joint contractures, and axial hypotonia with preserved antigravity limb movements. The ph
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amyotrophie spinale diaphragmatique type 2
SNOMEDCT-BE (disorder) / 770727008
SNOMEDCT-BE (disorder) / 770727008
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https://browser.ihtsdotools.or (...) [HTML]
IN-CONTEXT TRANSLATIONS


Others have searched : acute respiratory failure    chronic type 1 respiratory failure    chronic type ii respiratory failure    respiratory failure    


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'acute respiratory failure'

Date index:2023-12-08 -

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