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Translation of "Multiple anomalies " (English → French) :
TERMINOLOGY
see also In-Context Translations below 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 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
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 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 multiple congenital anomalies/dysmorphic syndrome with characteristics of multiple skeletal malformations (short femora and humeri, bilateral absence of metatarsal and metacarpal bone in hands and feet, bilateral partial syndactyly of fingers and t
syndrome de Verloove-Van Horick-Brubakk
SNOMEDCT-BE (short femora and humeri, bilateral absence of metatarsal and metacarpal bone in hands and feet, bilateral partial syndactyly of fingers and t / 764697003
SNOMEDCT-BE (disorder) / 764697003
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
Multiple epiphyseal dysplasia due to collagen 9 anomaly
dysplasie épiphysaire multiple due à une anomalie du collagène 9
SNOMEDCT-BE (disorder) / 766717008
SNOMEDCT-BE (disorder) / 766717008
A very rare multiple congenital anomalies syndrome described in three brothers of one South-African family, and with features of hypospadias and intellectual deficit, in association with microcephaly, craniofacial dysmorphism, joint laxity and beaked
syndrome d'hypospadias-déficience intellectuelle type Goldblatt
SNOMEDCT-BE (disorder) / 716096005
SNOMEDCT-BE (disorder) / 716096005
A multiple developmental anomalies syndrome with characteristics of neurological abnormalities (including megalencephaly, hypotonia, intellectual disability, abnormal EEG), dysmorphic facial features (high prominent forehead, grooved nasal tip, ptosi
syndrome neuro-facio-digito-rénal
SNOMEDCT-BE (including megalencephaly, hypotonia, intellectual disability, abnormal EEG), dysmorphic facial features (high prominent forehead, grooved nasal tip, ptosi / 725908007
SNOMEDCT-BE (disorder) / 725908007
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
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'Multiple anomalies'
Date index:2021-03-27 -
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