Vertaling van "Defibrination syndrome " (Engels → Nederlands) :

defibrination syndrome
defibrinatiesyndroom

Glomerular disorders in:cryoglobulinaemia (D89.1+) | disseminated intravascular coagulation [defibrination syndrome] (D65+) | haemolytic-uraemic syndrome (D59.3+) | Henoch(-Schönlein) purpura (D69.0+) | sickle-cell disorders (D57.-+)
glomerulaire aandoeningen bij | cryoglobulinemie (D89.1) | glomerulaire aandoeningen bij | gedissemineerde intravasale stolling [defibrinatiesyndroom] (D65) | glomerulaire aandoeningen bij | hemolytisch-uremisch syndroom (D59.3) | glomerulaire aandoeningen bij | purpura van Henoch(-Schönlein) (D69.0) | glomerulaire aandoeningen bij | sikkelcelaandoeningen (D57.-)

Afibrinogenaemia | Defibrination syndrome | Intravascular coagulation | following conditions classifiable to O00-O07
afibrinogenemiena aandoeningen geclassificeerd onder O00-O07 | defibrinatiesyndroomna aandoeningen geclassificeerd onder O00-O07 | intravasculaire stollingna aandoeningen geclassificeerd onder O00-O07

Disseminated intravascular coagulation [defibrination syndrome]
gedissemineerde intravasculaire stolling [defibrinatiesyndroom]

Miscarriage with defibrination syndrome
miskraam met verbruikscoagulopathie

defibrination
defibrinatie | defibrinatio

fragile x chromosome syndrome | fragile X syndrome | Fra-X syndrome | FRAXA syndrome | Martin-Bell syndrome | FRAX [Abbr.] | FXS [Abbr.]
fragiel-X-syndroom | FXS [Abbr.]

A group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandib
syndroom van Möbius

A rare malignant hematologic disease characterized by clonal proliferation of myeloid blasts, primarily involving the bone marrow, in association with congenital disorders (e.g. Fanconi anemia, dyskeratosis congenita, Bloom syndrome, Down syndrome, c
overgeërfde acute myeloïde leukemie

syndrome
syndroom | ziektebeeld