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Translation of "Syndrome des contractures congénitales létales type 2 " (French → English) :
TERMINOLOGY
see also In-Context Translations below syndrome des contractures congénitales létales type 2
Lethal congenital contracture syndrome type 2
SNOMEDCT-BE (disorder) / 715419004
SNOMEDCT-BE (disorder) / 715419004
syndrome des contractures congénitales létales type 3
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
syndrome des contractures congénitales létales type 1
Herva disease
SNOMEDCT-BE (disorder) / 715418007
SNOMEDCT-BE (disorder) / 715418007
myopathie létale congénitale type Compton-North
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
syndrome polymalformatif létal type Boissel
Lethal polymalformative syndrome Boissel type
SNOMEDCT-BE (disorder) / 778026007
SNOMEDCT-BE (disorder) / 778026007
Syndrome d'insuffisance thyroïdienne congénitale de type neurologique
Congenital iodine-deficiency syndrome, neurological type
WORLD HEALTH ORGANIZATION ICD-10: E00.0
WORLD HEALTH ORGANIZATION ICD-10: E00.0
Syndrome d'insuffisance thyroïdienne congénitale de type myxœdémateux
Congenital iodine-deficiency syndrome, myxoedematous type
WORLD HEALTH ORGANIZATION ICD-10: E00.1
WORLD HEALTH ORGANIZATION ICD-10: E00.1
Syndrome d'insuffisance thyroïdienne congénitale de type mixte
Congenital iodine-deficiency syndrome, mixed type
WORLD HEALTH ORGANIZATION ICD-10: E00.2
WORLD HEALTH ORGANIZATION ICD-10: E00.2
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Syndrome des contractures congénitales létales type 2
Date index:2024-04-12 -
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