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Myopathie létale congénitale type Compton-North
Syndrome des contractures congénitales létales type 1
Syndrome des contractures congénitales létales type 2
Syndrome des contractures congénitales létales type 3
Syndrome polymalformatif létal type Boissel

Translation of "Syndrome des contractures congénitales létales type 3 " (French → English) :

TERMINOLOGY
see also In-Context Translations below
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
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https://browser.ihtsdotools.or (...) [HTML]
syndrome des contractures congénitales létales type 2
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Lethal congenital contracture syndrome type 2
SNOMEDCT-BE (disorder) / 715419004
SNOMEDCT-BE (disorder) / 715419004
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https://browser.ihtsdotools.or (...) [HTML]
syndrome des contractures congénitales létales type 1
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Herva disease
SNOMEDCT-BE (disorder) / 715418007
SNOMEDCT-BE (disorder) / 715418007
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https://browser.ihtsdotools.or (...) [HTML]
myopathie létale congénitale type Compton-North
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A rare genetic lethal non-dystrophic congenital myopathy disorder characterized, antenatally, by fetal akinesia, intrauterine growth restriction and polyhydramnios, and, following birth, by severe neonatal hypotonia, severe generalized skeletal, bulb
SNOMEDCT-BE (disorder) / 773306002
SNOMEDCT-BE (disorder) / 773306002
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https://browser.ihtsdotools.or (...) [HTML]
syndrome polymalformatif létal type Boissel
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Lethal polymalformative syndrome Boissel type
SNOMEDCT-BE (disorder) / 778026007
SNOMEDCT-BE (disorder) / 778026007
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https://browser.ihtsdotools.or (...) [HTML]
Syndrome d'insuffisance thyroïdienne congénitale de type neurologique
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Congenital iodine-deficiency syndrome, neurological type
WORLD HEALTH ORGANIZATION ICD-10: E00.0
WORLD HEALTH ORGANIZATION ICD-10: E00.0
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
Syndrome d'insuffisance thyroïdienne congénitale de type myxœdémateux
https://icd.who.int/browse10/2 (...) (...) [HTML]
Congenital iodine-deficiency syndrome, myxoedematous type
WORLD HEALTH ORGANIZATION ICD-10: E00.1
WORLD HEALTH ORGANIZATION ICD-10: E00.1
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
Syndrome d'insuffisance thyroïdienne congénitale de type mixte
https://icd.who.int/browse10/2 (...) (...) [HTML]
Congenital iodine-deficiency syndrome, mixed type
WORLD HEALTH ORGANIZATION ICD-10: E00.2
WORLD HEALTH ORGANIZATION ICD-10: E00.2
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
IN-CONTEXT TRANSLATIONS


Others have searched : myopathie létale congénitale type compton-north    syndrome polymalformatif létal type boissel    Syndrome des contractures congénitales létales type 3    


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Syndrome des contractures congénitales létales type 3

Date index:2023-06-26 -

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