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Afibrinogenaemia
Birth defect
Congenital
Congenital afibrinogenaemia
Congenital afibrinogenaemia Deficiency AC globulin
Congenital anomaly
Congenital defect
Congenital deformity
Congenital disease
Congenital disorder
Congenital malformation
DIC
Defibrination syndrome
Deficiency of factor I
Fibrin-stabilizing
Fibrinogen
Following conditions classifiable to O00-O07
From birth
Fulminans
Hageman
II
Intravascular coagulation
Labile
Proaccelerin
Prothrombin
Stable
Stuart-Prower
V
VII
X
XII
XIII

Traduction de «congenital afibrinogenaemia » (Anglais → Néerlandais) :

congenital afibrinogenaemia

congenitale afibrinogenemie


Congenital afibrinogenaemia Deficiency:AC globulin | proaccelerin | Deficiency of factor:I [fibrinogen] | II [prothrombin] | V [labile] | VII [stable] | X [Stuart-Prower] | XII [Hageman] | XIII [fibrin-stabilizing] | Dysfibrinogenaemia (congenital) Hypoproconvertinaemia Owren's disease

congenitale afibrinogenemie | deficiëntie van | AC globuline | deficiëntie van | proaccelerine | deficiëntie van factor | I [fibrinogeen] | deficiëntie van factor | II [protrombine] | deficiëntie van factor | V [labiel] | deficiëntie van factor | VII [stabiel] | deficiëntie van factor | X [Stuart-Prower] | deficiëntie van factor | XII [Hageman] | deficiëntie van factor | XIII [fibrinestabiliserend] | dysfibrinogenemie (congenitaal) | hypoproconvertinemie | ziekte van Owren


birth defect | congenital anomaly | congenital defect | congenital disease | congenital disorder | congenital malformation

aangeboren aandoening


congenital disease [ congenital deformity | congenital malformation ]

aangeboren ziekte [ aangeboren afwijking ]


afibrinogenaemia

afibrinogeenaemia | afibrinogeenemie | afibrinogenemie


Afibrinogenaemia, acquired Consumption coagulopathy Diffuse or disseminated intravascular coagulation [DIC] Fibrinolytic haemorrhage, acquired Purpura:fibrinolytic | fulminans

afibrinogenemie, verworven | diffuse of gedissemineerde intravasculaire stolling [DIS] | fibrinolytische bloeding, verworven | purpura | fibrinolytisch | purpura | fulminans | verbruikscoagulopathie


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




Belongs to the group of multiple congenital anomalies/mental retardation syndromes with intellectual deficit, distinctive facies (upward slanting palpebral fissures, squint), kyphoscoliosis, diastasis recti, cryptorchidism, and a congenital heart def

syndroom van McDonough


Idiopathic congenital hypothyroidism is a type of primary congenital hypothyroidism whose cause and prevalence are unknown. Clinical manifestations are those of other forms of congenital hypothyroidism. Goiter is always absent. Ultrasound examination

idiopathische congenitale hypothyreoïdie




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Date index: 2023-09-07
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