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Translation of "aplasia " (English → French) :
TERMINOLOGY
see also In-Context Translations below aplasia | non-development of an organ
aplasie | croissance (incomplète ou insuffisante) d'un tissu ou d'un organe
UGENT - Medical terms -
UGENT - Medical terms -
Aplasia cutis with myopia syndrome
syndrome d'aplasie cutanée-myopie
SNOMEDCT-BE (disorder) / 720499004
SNOMEDCT-BE (disorder) / 720499004
Type 2 aplasia cutis
syndrome d'Adams-Oliver
SNOMEDCT-BE (disorder) / 34748004
SNOMEDCT-BE (disorder) / 34748004
Cutis aplasia
aplasia cutis congenita
SNOMEDCT-BE (disorder) / 35484002
SNOMEDCT-BE (disorder) / 35484002
Aplasia cutis congenita, nevus sebaceous syndrome
syndrome d'aplasie cutanée congénitale-naevus sébacé
SNOMEDCT-BE (disorder) / 774209001
SNOMEDCT-BE (disorder) / 774209001
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
syndrome d'aplasie cutanée congénitale-lymphangiectasie intestinale
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
SNOMEDCT-BE (disorder) / 720500008
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
aplasie cutanée congénitale autosomique récessive
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
SNOMEDCT-BE (disorder) / 720500008
Autosomal dominant aplasia and myelodysplasia
aplasie et myélodysplasie autosomiques dominantes
SNOMEDCT-BE (disorder) / 778006008
SNOMEDCT-BE (disorder) / 778006008
A lethal skeletal dysplasia with characteristics of cloverleaf skull anomaly, facial dysmorphism, limb shortness, splenic hypo/aplasia and radiological anomalies including thin tubular bones with flared metaphyses and deficient calvarial mineralisati
ostéocraniosténose
SNOMEDCT-BE (disorder) / 722109008
SNOMEDCT-BE (disorder) / 722109008
Adult pure red cell aplasia
aplasie pure des globules rouges de l'adulte
SNOMEDCT-BE (disorder) / 765748009
SNOMEDCT-BE (disorder) / 765748009
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'aplasia'
Date index:2023-03-27 -
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