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Translation of "Aplasie " (French → English) :
TERMINOLOGY
see also In-Context Translations below aplasie | croissance (incomplète ou insuffisante) d'un tissu ou d'un organe
aplasia | non-development of an organ
UGENT - Medical terms -
UGENT - Medical terms -
aplasie des muscles extenseurs des doigts et pouce-polyneuropathie
Hamanishi Ueba Tsuji syndrome
SNOMEDCT-BE (disorder) / 771261002
SNOMEDCT-BE (disorder) / 771261002
aplasie cutanée congénitale autosomique récessive
An extremely rare association syndrome, described in only two brothers to date (one of which died at 2 months of age), characterized by aplasia cutis congenita of the vertex and generalized edema (as well as hypoproteinemia and lymphopenia) due to in
SNOMEDCT-BE (disorder) / 720500008
SNOMEDCT-BE (one of which died at 2 months of age), characterised by aplasia cutis congenita of the vertex and generalised oedema (as well as hypoproteinaemia and lymphopenia) due to / 720500008
aplasie pure des globules rouges de l'adulte
Adult pure red cell aplasia
SNOMEDCT-BE (disorder) / 765748009
SNOMEDCT-BE (disorder) / 765748009
aplasie et myélodysplasie autosomiques dominantes
Autosomal dominant aplasia and myelodysplasia
SNOMEDCT-BE (disorder) / 778006008
SNOMEDCT-BE (disorder) / 778006008
syndrome d'hypoplasie ou aplasie du péroné, incurvation du fémur, oligodactylie
Fuhrmann syndrome (disorder)
SNOMEDCT-BE (disorder) / 721296004
SNOMEDCT-BE (disorder) / 721296004
syndrome d'aplasie cutanée congénitale-naevus sébacé
Aplasia cutis congenita, nevus sebaceous syndrome
SNOMEDCT-BE (disorder) / 774209001
SNOMEDCT-BE (disorder) / 774209001
syndrome d'aplasie cutanée-myopie
Aplasia cutis with myopia syndrome
SNOMEDCT-BE (disorder) / 720499004
SNOMEDCT-BE (disorder) / 720499004
syndrome d'aplasie cutanée congénitale-lymphangiectasie intestinale
An extremely rare association syndrome, described in only two brothers to date (one of which died at 2 months of age), characterised by aplasia cutis congenita of the vertex and generalised oedema (as well as hypoproteinaemia and lymphopenia) due to
SNOMEDCT-BE (disorder) / 720500008
SNOMEDCT-BE (one of which died at 2 months of age), characterised by aplasia cutis congenita of the vertex and generalised oedema (as well as hypoproteinaemia and lymphopenia) due to / 720500008
hyperhidrose, caries prématurées et aplasie des prémolaires
Book's syndrome
SNOMEDCT-CA (constatation) / 239045006
SNOMEDCT-CA (constatation) / 239045006
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Aplasie
Date index:2023-11-27 -
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