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Translation of "congenital anomaly " (English → French) :
TERMINOLOGY
see also In-Context Translations below A rare congenital anomaly of the great veins with characteristics of an anomalous course of the left brachiocephalic vein, passing from left to right below the aortic arch and entering the superior vena cava below the orifice of the azygos vein. Pati
veine innominée sous-aortique
SNOMEDCT-BE (disorder) / 766756002
SNOMEDCT-BE (disorder) / 766756002
Congenital anomaly
malformation congénitale
SNOMEDCT-BE (disorder) / 276654001
SNOMEDCT-BE (disorder) / 276654001
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
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
Belongs to the group of multiple congenital anomalies/mental retardation syndromes with intellectual deficit, distinctive facies (upward slanting palpebral fissures, squint), kyphoscoliosis, diastasis recti, cryptorchidism, and a congenital heart def
syndrome de McDonough
SNOMEDCT-BE (upward slanting palpebral fissures, squint), kyphoscoliosis, diastasis recti, cryptorchidism, and a congenital heart def / 715441004
SNOMEDCT-BE (disorder) / 715441004
A rare genetic multiple congenital anomalies syndrome with characteristics of second branchial arch anomalies (branchial cysts and fistulae), malformations of the outer, middle and inner ear associated with sensorineural, mixed or conductive hearing
syndrome branchio-otique
SNOMEDCT-BE (branchial cysts and fistulae), malformations of the outer, middle and inner ear associated with sensorineural, mixed or conductive hearing / 764810000
SNOMEDCT-BE (disorder) / 764810000
Congenital:anomaly | deformity | disease or lesion | multiple anomalies | NOS of brain
Anomalie congénitale | Anomalies multiples congénitales | Maladie ou lésion congénitale | SAI de l'encéphale
WORLD HEALTH ORGANIZATION ICD-10: Q04.9
WORLD HEALTH ORGANIZATION ICD-10: Q04.9
A rare multiple congenital anomalies syndrome with characteristics of mild intellectual disability, short stature, cardiac anomalies, mild dysmorphic features (macrocephaly, prominent forehead, hypertelorism, exophthalmos), cutis laxa, joint hyperlax
syndrome cranio-facio-fronto-digital
SNOMEDCT-BE (macrocephaly, prominent forehead, hypertelorism, exophthalmos), cutis laxa, joint hyperlax / 763320005
SNOMEDCT-BE (disorder) / 763320005
A rare chromosomal anomaly with characteristics of prenatal and postnatal growth retardation, developmental delay, intellectual impairment, dysmorphic signs and variable combination of congenital anomalies, including cardiovascular, genitourinary and
syndrome de microduplication 3q26
SNOMEDCT-BE (disorder) / 778073001
SNOMEDCT-BE (disorder) / 778073001
A rare multiple congenital anomalies/dysmorphic syndrome with characteristics of male, 46,XY gonadal dysgenesis, cleft palate, micrognathia, conotruncal heart defects and unspecific skeletal, brain and kidney anomalies.
syndrome génito-palato-cardiaque
SNOMEDCT-BE (disorder) / 773749003
SNOMEDCT-BE (disorder) / 773749003
A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of cerebellar-like ataxia, photosensitivity (mainly of the face and trunk), short stature and intellectual disability. Additional features include clinodactyly, sin
syndrome d'ataxie-photosensibilité-petite taille
SNOMEDCT-BE (mainly of the face and trunk), short stature and intellectual disability. Additional features include clinodactyly, sin / 773769008
SNOMEDCT-BE (disorder) / 773769008
www.wordscope.com (v4.0.br.77)
'congenital anomaly'
Date index:2023-09-24 -
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