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Translation of "failure " (English → French) :

A rare intestinal disorder of neonates of unknown aetiology. Patients are born with a short small bowel (less than 75 cm in length) that compromises proper intestinal absorption and leads chronic diarrhoea, vomiting and failure to thrive.
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syndrome du grêle court congénital
SNOMEDCT-BE (less than 75 cm in length) that compromises proper intestinal absorption and leads chronic diarrhoea, vomiting and failure to thrive. / 715201005
SNOMEDCT-BE (disorder) / 715201005
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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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Death or serious disability (kernicterus) associated with failure to identify and treat hyperbilirubinemia in neonates
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mort ou un handicap sérieux (kernictère) associés avec à l'absence de dépistage et de traitement de l'hyperbilirubinémie chez les nouveau-nés
SNOMEDCT-BE (kernicterus) associated with failure to identify and treat hyperbilirubinemia in neonates / 370914009
SNOMEDCT-BE (kernictère) associés avec à l'absence de dépistage et de traitement de l'hyperbilirubinémie chez les nouveau-nés / 370914009
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A rare chromosomal anomaly syndrome with characteristics of mild global developmental delay/intellectual disability with poor to absent speech, dysmorphic features (long midface, retrognathia with overbite, protruding ears), microcephaly, failure to
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syndrome de microdélétion 17p13.1 distale
SNOMEDCT-BE (long midface, retrognathia with overbite, protruding ears), microcephaly, failure to / 770629000
SNOMEDCT-BE (disorder) / 770629000
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An extremely rare inborn error of sterol biosynthesis with manifestations of facial dysmorphism, congenital anomalies (including limb and kidney anomalies), failure to thrive, developmental delay and liver disease. Only 4 cases have been reported in
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lathostérolose
SNOMEDCT-BE (including limb and kidney anomalies), failure to thrive, developmental delay and liver disease. Only 4 cases have been reported in / 719257008
SNOMEDCT-BE (disorder) / 719257008
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A rare inherited bone marrow failure syndrome with manifestation of an isolated and severe decrease in the number of platelets and megakaryocytes during the first years of life that develops into bone marrow failure with pancytopenia later in childho
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thrombocytopénie amégacaryocytaire congénitale
SNOMEDCT-BE (disorder) / 716336002
SNOMEDCT-BE (disorder) / 716336002
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Congestive heart disease Right ventricular failure (secondary to left heart failure)
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Insuffisance ventriculaire droite (secondaire à une insuffisance cardiaque gauche) Maladie congestive du cœur
WORLD HEALTH ORGANIZATION ICD-10: I50.0
WORLD HEALTH ORGANIZATION ICD-10: I50.0
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Hypertensive heart and renal disease with both (congestive) heart failure and renal failure
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Cardionéphropathie hypertensive, avec insuffisance cardiaque (congestive) et rénale
WORLD HEALTH ORGANIZATION ICD-10: I13.2
WORLD HEALTH ORGANIZATION ICD-10: I13.2
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https://icd.who.int/browse10/2 (...) [HTML]
A rare genetic hepatic disease characterized by massive hepatomegaly, moderate to severe transient hypertriglyceridemia and hepatic steatosis (followed by fibrosis) manifesting in infancy with failure to thrive, vomiting, an enlarged abdomen and a fa
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hypertriglycéridémie transitoire et stéatose hépatique du nourrisson
SNOMEDCT-CA (followed by fibrosis) manifesting in infancy with failure to thrive, vomiting, an enlarged abdomen and a fa / 773649005
SNOMEDCT-CA (trouble) / 773649005
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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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'failure'

Date index:2022-05-08 -

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