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Syndrome d'Ehlers-Danlos par déficit en tenascin-X
Syndrome de Laron avec déficit immunitaire
Syndrome de déficit Rh

Translation of "syndrome de déficit rh " (French → English) :

TERMINOLOGY
see also In-Context Translations below
syndrome de déficit Rh

Rh deficiency syndrome
SNOMEDCT-BE (disorder) / 37272000
SNOMEDCT-BE (disorder) / 37272000


syndrome de déficit constitutionnel de la réparation des mésappariements

A rare inherited cancer-predisposing syndrome characterized by the development of a broad spectrum of malignancies during childhood, including mainly brain, hematological and gastrointestinal cancers, although embryonic and other tumors have also bee
SNOMEDCT-BE (disorder) / 764946008
SNOMEDCT-BE (disorder) / 764946008


syndrome de déficit en stéroïde déshydrogénase-anomalies dentaires

Lyngstadaas syndrome
SNOMEDCT-BE (disorder) / 723583009
SNOMEDCT-BE (disorder) / 723583009


syndrome d'hypercoagulabilité par déficit héréditaire en glycosyl phosphatidyl inositol

The combination of a propensity for venous thrombosis and seizures has been reported in two unrelated kindreds. Transmission is autosomal recessive. It results from a point mutation of PIGM, which reduces transcription of PIGM and blocks mannosylatio
SNOMEDCT-BE (disorder) / 724344004
SNOMEDCT-BE (disorder) / 724344004


syndrome de dysmorphie faciale-déficit immunitaire-livedo-petite taille

Facial dysmorphism, immunodeficiency, livedo, short stature syndrome
SNOMEDCT-BE (disorder) / 771515001
SNOMEDCT-BE (disorder) / 771515001


syndrome d'Ehlers-Danlos par déficit en tenascin-X

Ehlers-Danlos syndrome classic-like type
SNOMEDCT-BE (disorder) / 778022009
SNOMEDCT-BE (disorder) / 778022009


syndrome de fibrose pulmonaire-déficit immunitaire-dysgénésie gonadique 46,XX

Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome
SNOMEDCT-BE (disorder) / 721977007
SNOMEDCT-BE (disorder) / 721977007


syndrome d'ataxie cérébelleuse autosomique dominante-épilepsie-déficience intellectuelle par déficit de TUD

Spinocerebellar ataxia autosomal recessive type 23
SNOMEDCT-BE (disorder) / 773498006
SNOMEDCT-BE (disorder) / 773498006


syndrome de troubles sévères de l'alimentation-retard staturo-pondéral-microcéphalie par déficit en ASXL3

Bainbridge Roppers syndrome
SNOMEDCT-BE (disorder) / 773400009
SNOMEDCT-BE (disorder) / 773400009


syndrome de Laron avec déficit immunitaire

Laron-like syndrome
SNOMEDCT-BE (disorder) / 724179008
SNOMEDCT-BE (disorder) / 724179008
IN-CONTEXT TRANSLATIONS


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syndrome de déficit rh

Date index:2022-08-25 -

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