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Anaemia Addison
Antibiotic resistance plasmid
Appraise risk factors
Assess risk factors
Biermer
Check risk factors
Congenital afibrinogenaemia Deficiency AC globulin
Congenital intrinsic factor deficiency
Deficiency of factor I
Drug-resistance factor
Factor XII
Fibrin-stabilizing
Fibrinogen
Hageman
Hageman factor
Hageman-factor deficiency
II
Labile
Pernicious
Proaccelerin
Prothrombin
R-factor
R-factor plasmid
R-plasmid
Resistance factor
Resistance plasmid
Risk factor assessment
Stable
Stuart-Prower
V
VII
X
XII
XIII

Vertaling van "Hageman factor " (Engels → Nederlands) :



Hageman-factor deficiency

factor XII-deficiëntie | Hageman-factor deficiëntie


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


Short stature due to primary acid-labile subunit (ALS) deficiency is characterized by moderate postnatal growth deficit, markedly low circulating levels of insulin-like growth factor 1 (IGF-1) and insulin-like growth factor binding protein 3 (IGFBP-3

kleine gestalte door primaire zuurlabiele subeenheiddeficiëntie


appraise risk factors | check risk factors | assess risk factors | risk factor assessment

risicofactoren beoordelen | risicofactoren inschatten


antibiotic resistance plasmid | drug-resistance factor | resistance factor | resistance plasmid | R-factor | R-factor plasmid | R-plasmid

resistentie-factor | R-factor


An inherited bleeding disorder caused by the reduction in activity and antigen levels of both factor V and factor VIII with manifestation of mild-to-moderate bleeding symptoms. Caused by mutations either in the LMAN1 gene (chromosome 18; q21) or in t

gecombineerde deficiëntie van factor V en factor VIII


Syndrome that is characterized by the association of multiple sclerosis with lamellar ichthyosis and hematological anomalies (beta thalassemia minor and a quantitative deficit of factor VIII-von Willebrand complex). Other clinical manifestations may

multiple sclerose, ichthyosis, factor VIII-deficiëntiesyndroom


Anaemia:Addison | Biermer | pernicious (congenital) | Congenital intrinsic factor deficiency

anemie van | Addison | anemie van | Biermer | congenitale 'intrinsic factor'-deficiëntie | pernicieuze anemie (congenitaal)


Vitamin B12 deficiency anaemia due to intrinsic factor deficiency

anemie door vitamine B12-deficiëntie als gevolg van tekort aan 'intrinsic factor'




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'Hageman factor' ->

Date index: 2022-04-27
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