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Syndrome
Syndrome faciodigitogénital autosomique récessif
Synostose huméro-cubitale
Synostose huméro-radiale
Synostose huméro-radio-cubitale
Synostose tibio-fibulaire

Translation of "syndrome de synostose " (French → English) :

syndrome de synostose radio-ulnaire-microcéphalie-scoliose

Giuffre Tsukahara syndrome
SNOMEDCT-BE (disorder) / 719162001
SNOMEDCT-BE (disorder) / 719162001


synostose huméro-cubitale

Humeroulnar synostosis
SNOMEDCT-BE (disorder) / 205330003
SNOMEDCT-BE (disorder) / 205330003


synostose huméro-radiale

Humeroradial synostosis
SNOMEDCT-BE (disorder) / 205329008
SNOMEDCT-BE (disorder) / 205329008


synostose tibio-fibulaire

Congenital tibio-fibular fusion
SNOMEDCT-BE (disorder) / 737581000
SNOMEDCT-BE (disorder) / 737581000


synostose huméro-radio-cubitale

Humero-radio-ulnar fusion
SNOMEDCT-BE (disorder) / 773733000
SNOMEDCT-BE (disorder) / 773733000




syndrome d'atrophie spinale-ophtalmoplégie-syndrome pyramidal

Hamano Tsukamoto syndrome
SNOMEDCT-BE (disorder) / 771238004
SNOMEDCT-BE (disorder) / 771238004


syndrome de déficience intellectuelle liée à l'X-syndrome cranio-facio-squelettique

A rare hereditary syndromic intellectual disability with characteristics of craniofacial and skeletal abnormalities in association with mild intellectual disability in females and early postnatal lethality in males. In addition to mild cognitive impa
SNOMEDCT-BE (disorder) / 773274001
SNOMEDCT-BE (disorder) / 773274001


syndrome de neuropathie périphérique-leucodystrophie centrale dysmyélinisante-syndrome de Waardenburg-maladie de Hirschsprung

Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease
SNOMEDCT-BE (disorder) / 765325002
SNOMEDCT-BE (disorder) / 765325002


syndrome faciodigitogénital autosomique récessif

Aarskog-like syndrome
SNOMEDCT-BE (disorder) / 725434009
SNOMEDCT-BE (disorder) / 725434009




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syndrome de synostose

Date index:2021-02-04 -

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