| D68.0 |
Von Willebrand's disease
Angiohaemophilia
Factor VIII deficiency with vascular defect
Vascular haemophilia
Excludes:
- capillary fragility (hereditary) ( D69.8 )
- factor VIII deficiency:
- NOS ( D66 )
- with functional defect ( D66 )
|
| D68.1 |
Hereditary factor XI deficiency
Haemophilia C
Plasma thromboplastin antecedent [PTA] deficiency
|
| D68.2 |
Hereditary deficiency of other clotting factors
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
|
| D68.3 |
Haemorrhagic disorder due to circulating anticoagulants
Haemorrhage during long-term use of anticoagulants
Hyperheparinaemia
Increase in:
antithrombin
anti-VIIIa
anti-IXa
anti-Xa
anti-XIa
Use additional external cause code (Chapter XX), if desired, to identify any administered anticoagulant
Excludes:
- long-term use of anticoagulants without haemorrhage (Z92.1)
|
| D68.4 |
Acquired coagulation factor deficiency
Deficiency of coagulation factor due to:
liver disease
vitamin K deficiency
Excludes:
- vitamin K deficiency of newborn ( P53 )
|
| D68.8 |
Other specified coagulation defects
Presence of systemic lupus erythematosus [SLE] inhibitor
|
| D68.9 |
Coagulation defect, unspecified
|