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ICD-10-CM-2023 Diagnosis Codes Overview
ICD-10-CM-2023 > D50-D89 > D65-D69 > D68
D65-D69
Coagulation defects, purpura and other hemorrhagic conditions
D68

Other coagulation defects

Excl1.:
abnormal coagulation profile NOS (R79.1)
Excl2.:
coagulation defects complicating abortion or ectopic or molar pregnancy (O00-O07, O08.1)
coagulation defects complicating pregnancy, childbirth and the puerperium (O45.0, O46.0, O67.0, O72.3)
D68.0

Von Willebrand disease

Excl1.:
capillary fragility (hereditary) (D69.8)
factor VIII deficiency NOS (D66)
factor VIII deficiency with functional defect (D66)
D68.00
Von Willebrand disease, unspecified
D68.01
Von Willebrand disease, type 1
Info:
Partial quantitative deficiency of von Willebrand factor
Type 1C von Willebrand disease
D68.02
Von Willebrand disease, type 2
Info:
Qualitative defects of von Willebrand factor
D68.020
Von Willebrand disease, type 2A
Info:
Qualitative defects of von Willebrand factor with decreased platelet adhesion and selective deficiency of high-molecular-weight multimers
D68.021
Von Willebrand disease, type 2B
Info:
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
D68.022
Von Willebrand disease, type 2M
Info:
Qualitative defects of von Willebrand factor with defective platelet adhesion with a normal size distribution of von Willebrand factor multimers
D68.023
Von Willebrand disease, type 2N
Info:
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
D68.029
Von Willebrand disease, type 2, unspecified
Info:
Qualitative defect in von Willebrand factor function, with no further subtyping
D68.03
Von Willebrand disease, type 3
Info:
(Near) complete absence of von Willebrand factor
Total quantitative deficiency of von Willebrand factor
D68.04
Acquired von Willebrand disease
Info:
Acquired von Willebrand syndrome
D68.09
Other von Willebrand disease
Info:
Platelet-type von Willebrand disease
Pseudo-von Willebrand disease
Use add'l
, if applicable, qualitative platelet defects (D69.1)
D68.1
Hereditary factor XI deficiency
Info:
Hemophilia C
Plasma thromboplastin antecedent [PTA] deficiency
Rosenthal's disease
D68.2
Hereditary deficiency of other clotting factors
Info:
AC globulin deficiency
Congenital afibrinogenemia
Deficiency of factor I [fibrinogen]
Deficiency of factor II [prothrombin]
Deficiency of factor V [labile]
Deficiency of factor VII [stable]
Deficiency of factor X [Stuart-Prower]
Deficiency of factor XII [Hageman]
Deficiency of factor XIII [fibrin stabilizing]
Dysfibrinogenemia (congenital)
Hypoproconvertinemia
Owren's disease
Proaccelerin deficiency
D68.3

Hemorrhagic disorder due to circulating anticoagulants

D68.31
Hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
D68.311
Acquired hemophilia
Info:
Autoimmune hemophilia
Autoimmune inhibitors to clotting factors
Secondary hemophilia
D68.312
Antiphospholipid antibody with hemorrhagic disorder
Info:
Lupus anticoagulant (LAC) with hemorrhagic disorder
Systemic lupus erythematosus [SLE] inhibitor with hemorrhagic disorder
Excl1.:
antiphospholipid antibody, finding without diagnosis (R76.0)
antiphospholipid antibody syndrome (D68.61)
antiphospholipid antibody with hypercoagulable state (D68.61)
lupus anticoagulant (LAC) finding without diagnosis (R76.0)
lupus anticoagulant (LAC) with hypercoagulable state (D68.62)
systemic lupus erythematosus [SLE] inhibitor finding without diagnosis (R76.0)
systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (D68.62)
D68.318
Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
Info:
Antithromboplastinemia
Antithromboplastinogenemia
Hemorrhagic disorder due to intrinsic increase in antithrombin
Hemorrhagic disorder due to intrinsic increase in anti-VIIIa
Hemorrhagic disorder due to intrinsic increase in anti-IXa
Hemorrhagic disorder due to intrinsic increase in anti-XIa
D68.32
Hemorrhagic disorder due to extrinsic circulating anticoagulants
Info:
Drug-induced hemorrhagic disorder
Hemorrhagic disorder due to increase in anti-IIa
Hemorrhagic disorder due to increase in anti-Xa
Hyperheparinemia
Use add'l
code for adverse effect, if applicable, to identify drug (T45.515, T45.525)
D68.4
Acquired coagulation factor deficiency
Info:
Deficiency of coagulation factor due to liver disease
Deficiency of coagulation factor due to vitamin K deficiency
Excl1.:
vitamin K deficiency of newborn (P53)
D68.5

Primary thrombophilia

Info:
Primary hypercoagulable states
Excl1.:
antiphospholipid syndrome (D68.61)
lupus anticoagulant (D68.62)
secondary activated protein C resistance (D68.69)
secondary antiphospholipid antibody syndrome (D68.69)
secondary lupus anticoagulant with hypercoagulable state (D68.69)
secondary systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (D68.69)
systemic lupus erythematosus [SLE] inhibitor finding without diagnosis (R76.0)
systemic lupus erythematosus [SLE] inhibitor with hemorrhagic disorder (D68.312)
thrombotic thrombocytopenic purpura (M31.19)
D68.51
Activated protein C resistance
Info:
Factor V Leiden mutation
D68.52
Prothrombin gene mutation
D68.59
Other primary thrombophilia
Info:
Antithrombin III deficiency
Hypercoagulable state NOS
Primary hypercoagulable state NEC
Primary thrombophilia NEC
Protein C deficiency
Protein S deficiency
Thrombophilia NOS
D68.6

Other thrombophilia

Info:
Other hypercoagulable states
Excl1.:
diffuse or disseminated intravascular coagulation [DIC] (D65)
heparin induced thrombocytopenia (HIT) (D75.82-)
hyperhomocysteinemia (E72.11)
D68.61
Antiphospholipid syndrome
Info:
Anticardiolipin syndrome
Antiphospholipid antibody syndrome
Excl1.:
anti-phospholipid antibody, finding without diagnosis (R76.0)
anti-phospholipid antibody with hemorrhagic disorder (D68.312)
lupus anticoagulant syndrome (D68.62)
D68.62
Lupus anticoagulant syndrome
Info:
Lupus anticoagulant
Presence of systemic lupus erythematosus [SLE] inhibitor
Excl1.:
anticardiolipin syndrome (D68.61)
antiphospholipid syndrome (D68.61)
lupus anticoagulant (LAC) finding without diagnosis (R76.0)
lupus anticoagulant (LAC) with hemorrhagic disorder (D68.312)
D68.69
Other thrombophilia
Info:
Hypercoagulable states NEC
Secondary hypercoagulable state NOS
D68.8
Other specified coagulation defects
Excl1.:
hemorrhagic disease of newborn (P53)
D68.9
Coagulation defect, unspecified

 

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