D65-D69 Coagulation defects, purpura and other haemorrhagic conditions

 
Chapter III

Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
(D50-D89)

Coagulation defects, purpura and other haemorrhagic conditions
(D65-D69)

D65		Disseminated intravascular coagulation [defibrination syndrome] Latin: Coagulatio intravascularis disseminata
		Afibrinogenaemia, acquired Consumption coagulopathy Diffuse or disseminated intravascular coagulation[DIC] Fibrinolytic haemorrhage, acquired Purpura: · fibrinolytic · fulminans
		Excludes:	that (complicating): · abortion or ectopic or molar pregnancy (O00-O07, O08.1) · in newborn (P60) · pregnancy, childbirth and the puerperium (O45.0, O46.0, O67.0, O72.3)

D66		Hereditary factor VIII deficiency Latin: Haemophilia A propter deficientiam factoris VIII
		Deficiency factor VIII (with functional defect) Haemophilia: · NOS · A · classical
		Excludes:	factor VIII deficiency with vascular defect (D68.0)

D67		Hereditary factor IX deficiency Latin: Haemophilia B propter deficientiam factoris IX
		Christmas disease Deficiency: · factor IX (with functional defect) · plasma thromboplastin component [PTC] Haemophilia B

D68		Other coagulation defects Latin: Defectus coagulationis alii
		Excludes:	those complicating: · abortion or ectopic or molar pregnancy (O00-O07, O08.1) · pregnancy, childbirth and the puerperium (O45.0, O46.0, O67.0, O72.3)
D68.0		Von Willebrand's disease Latin: Morbus von Willebrand
		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 Latin: Deficientia factoris IX hereditaria
		Haemophilia C Plasma thromboplastin antecedent [PTA] deficiency
D68.2		Hereditary deficiency of other clotting factors Latin: Deficientia factorum coagulationis aliorum hereditaria
		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 Latin: Disordo haemorrhagicus propter anticoagulantes circulatorios
		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 Latin: Deficientia factoris coagulationis acquisita
		Deficiency of coagulation factor due to: · liver disease · vitamin K deficiency
		Excludes:	vitamin K deficiency of newborn (P53)
D68.8		Other specified coagulation defects Latin: Defectus coagulationis specificati alii
		Presence of systemic lupus erythematosus [SLE] inhibitor
D68.9		Coagulation defect, unspecified Latin: Defectus coagulationis, non specificatus

D69		Purpura and other haemorrhagic conditions Latin: Purpura et status haemorrhagici alii
		Excludes:	benign hypergammaglobulinaemic purpura (D89.0) cryoglobulinaemic purpura (D89.1) essential (haemorrhagic) thrombocythaemia (D47.3) purpura fulminans (D65) thrombotic thrombocytopenic purpura (M31.1)
D69.0		Allergic purpura Latin: Purpura allergica
		Purpura: · anaphylactoid · Henoch(-Schönlein) · nonthrombocytopenic:   · haemorrhagic   · idiopathic · vascular Vasculitis, allergic
D69.1		Qualitative platelet defects Latin: Defectus trombocytorum qualitativi
		Bernard-Soulier [giant platelet] syndrome Glanzmann's disease Grey platelet syndrome Thromboasthenia (haemorrhagic)(hereditary) Thrombocytopathy
		Excludes:	von Willebrand's disease (D68.0)
D69.2		Other nonthrombocytopenic purpura Latin: Purpura non thrombocytopenica alia
		Purpura: · NOS · senile · simplex
D69.3		Idiopathic thrombocytopenic purpura Latin: Purpura thrombocytopenica idiopathica
		Evans' syndrome
D69.4		Other primary thrombocytopenia Latin: Thrombocytopenia primaria alia
		Excludes:	thrombocytopenia with absent radius (Q87.2) transient neonatal thrombocytopenia (P61.0) Wiskott-Aldrich syndrome (D82.0)
D69.5		Secondary thrombocytopenia Latin: Thrombocytopenia secundaria
		Use additional external cause code (Chapter XX), if desired, to identify cause.
D69.6		Thrombocytopenia, unspecified Latin: Thrombocytopenia, non specificata
D69.8		Other specified haemorrhagic conditions Latin: Status haemorrhagici specificati, alii
		Capillary fragility (hereditary) Vascular pseudohaemophilia
D69.9		Haemorrhagic condition, unspecified Latin: Status haemorrhagicus, non specificatus

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