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Pneumopathie de la rubéole congénitale
Rubéole congénitale évolutive
Syndrome de cardiopathie congénitale-membres courts
Syndrome de malformation congénitale
Syndrome de rubéole congénitale
Syndrome des contractures congénitales létales type 1
Syndrome des contractures congénitales létales type 3

Translation of "syndrome de rubéole congénitale " (French → English) :

syndrome de rubéole congénitale
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Congenital rubella
SNOMEDCT-BE (disorder) / 1857005
SNOMEDCT-BE (disorder) / 1857005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Syndrome de rubéole congénitale
https://icd.who.int/browse10/2 (...) (...) [HTML]
Congenital rubella syndrome
WORLD HEALTH ORGANIZATION ICD-10: P35.0
WORLD HEALTH ORGANIZATION ICD-10: P35.0
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
pneumopathie de la rubéole congénitale
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Congenital rubella pneumonitis
SNOMEDCT-CA (trouble) / 47082005
SNOMEDCT-CA (trouble) / 47082005
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https://browser.ihtsdotools.or (...) [HTML]
rubéole congénitale évolutive
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Expanded rubella syndrome
SNOMEDCT-CA (trouble) / 79303006
SNOMEDCT-CA (trouble) / 79303006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Pneumopathie de la rubéole congénitale
https://icd.who.int/browse10/2 (...) (...) [HTML]
Congenital rubella pneumonitis
WORLD HEALTH ORGANIZATION ICD-10: P35.0
WORLD HEALTH ORGANIZATION ICD-10: P35.0
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
syndrome de cardiopathie congénitale-face ronde-petite taille
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A very rare syndrome described in three siblings of one Japanese family with main features of congenital heart disease, round face with depressed nasal bridge, small mouth, short stature, and relatively dark skin and typical dermatoglyphic anomalies,
SNOMEDCT-BE (disorder) / 715987000
SNOMEDCT-BE (disorder) / 715987000
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https://browser.ihtsdotools.or (...) [HTML]
syndrome de malformation congénitale
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Multiple congenital anomalies
SNOMEDCT-BE (disorder) / 400038003
SNOMEDCT-BE (disorder) / 400038003
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https://browser.ihtsdotools.or (...) [HTML]
syndrome de cardiopathie congénitale-membres courts
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Cardioskeletal syndrome Kuwaiti type
SNOMEDCT-BE (disorder) / 721009008
SNOMEDCT-BE (disorder) / 721009008
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https://browser.ihtsdotools.or (...) [HTML]
syndrome des contractures congénitales létales type 3
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Identified in Israeli Bedouin kindred the phenotype is similar to that of Lethal congenital contracture syndrome type 2 but without distended bladder. Affected individuals are born with severe multiple joint contractures with severe muscle wasting an
SNOMEDCT-BE (disorder) / 715420005
SNOMEDCT-BE (disorder) / 715420005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
syndrome des contractures congénitales létales type 1
https://browser.ihtsdotools.or (...) (...) [HTML]
Herva disease
SNOMEDCT-BE (disorder) / 715418007
SNOMEDCT-BE (disorder) / 715418007
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]


Others have searched : pneumopathie de la rubéole congénitale    syndrome de rubéole congénitale    rubéole congénitale évolutive    syndrome de cardiopathie congénitale-membres courts    syndrome de malformation congénitale    


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syndrome de rubéole congénitale

Date index:2023-01-16 -

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