Von Willebrand disease
Notes: Partial quantitative deficiency of von Willebrand factor ; Type 1C von Willebrand disease ; Qualitative defects of von Willebrand factor ; Qualitative defects of von Willebrand factor with decreased platelet adhesion and selective deficiency of high-molecular-weight multimers ; Qualitative defects of von Willebrand factor with high-molecular-weight von Willebrand factor loss ; Qualitative defects of von Willebrand factor with hyper-adhesive forms ; Qualitative defects of von Willebrand factor with increased affinity for platelet glycoprotein lb ; Qualitative defects of von Willebrand factor with defective platelet adhesion with a normal size distribution of von Willebrand factor multimers ; Qualitative defects of von Willebrand factor with defective von Willebrand factor to factor VIII binding ; Qualitative defects of von Willebrand factor with markedly decreased affinity for factor VIII ; Qualitative defect in von Willebrand factor function, with no further subtyping ; (Near) complete absence of von Willebrand factor ; Total quantitative deficiency of von Willebrand factor ; Acquired von Willebrand syndrome ; Platelet-type von Willebrand disease ; Pseudo-von Willebrand disease ; capillary fragility (hereditary) (D69.8) ; factor VIII deficiency NOS (D66) ; factor VIII deficiency with functional defect (D66)
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