2019/2020

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DRG 813

Coagulation disorders

  • D65
    Disseminated intravascular coagulation [defibrination syndrome]
  • D66
    Hereditary factor VIII deficiency
  • D67
    Hereditary factor IX deficiency
  • D68.0
    Von Willebrand's disease
  • D68.1
    Hereditary factor XI deficiency
  • D68.2
    Hereditary deficiency of other clotting factors
  • D68.311
    Acquired hemophilia
  • D68.318
    Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
  • D68.32
    Hemorrhagic disorder due to extrinsic circulating anticoagulants
  • D68.4
    Acquired coagulation factor deficiency
  • D68.8
    Other specified coagulation defects
  • D68.9
    Coagulation defect, unspecified
  • D69.0
    Allergic purpura
  • D69.1
    Qualitative platelet defects
  • D69.2
    Other nonthrombocytopenic purpura
  • D69.3
    Immune thrombocytopenic purpura
  • D69.41
    Evans syndrome
  • D69.42
    Congenital and hereditary thrombocytopenia purpura
  • D69.49
    Other primary thrombocytopenia
  • D69.51
    Posttransfusion purpura
  • D69.59
    Other secondary thrombocytopenia
  • D69.6
    Thrombocytopenia, unspecified
  • D69.8
    Other specified hemorrhagic conditions
  • D69.9
    Hemorrhagic condition, unspecified
  • D75.82
    Heparin induced thrombocytopenia (HIT)
  • R23.3
    Spontaneous ecchymoses
ICD-10-CM D65

Disseminated intravascular coagulation [defibrination syndrome]

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Afibrinogenemia, acquired
  • Consumption coagulopathy
  • Diffuse or disseminated intravascular coagulation [DIC]
  • Fibrinolytic hemorrhage, acquired
  • Fibrinolytic purpura
  • Purpura fulminans
Type 1 Excludes
  • disseminated intravascular coagulation (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)
ICD-10-CM D66

Hereditary factor VIII deficiency

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Classical hemophilia
  • Deficiency factor VIII (with functional defect)
  • Hemophilia NOS
  • Hemophilia A
Type 1 Excludes
  • factor VIII deficiency with vascular defect (D68.0)
ICD-10-CM D67

Hereditary factor IX deficiency

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Christmas disease
  • Factor IX deficiency (with functional defect)
  • Hemophilia B
  • Plasma thromboplastin component [PTC] deficiency
ICD-10-CM D68.0

Von Willebrand's disease

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Angiohemophilia
  • Factor VIII deficiency with vascular defect
  • Vascular hemophilia
Type 1 Excludes
  • capillary fragility (hereditary) (D69.8)
  • factor VIII deficiency NOS (D66)
  • factor VIII deficiency with functional defect (D66)
ICD-10-CM D68.1

Hereditary factor XI deficiency

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Hemophilia C
  • Plasma thromboplastin antecedent [PTA] deficiency
  • Rosenthal's disease
ICD-10-CM D68.2

Hereditary deficiency of other clotting factors

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • 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
ICD-10-CM D68.311

Acquired hemophilia

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Autoimmune hemophilia
  • Autoimmune inhibitors to clotting factors
  • Secondary hemophilia
ICD-10-CM D68.318

Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • 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
ICD-10-CM D68.32

Hemorrhagic disorder due to extrinsic circulating anticoagulants

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Drug-induced hemorrhagic disorder
  • Hemorrhagic disorder due to increase in anti-IIa
  • Hemorrhagic disorder due to increase in anti-Xa
  • Hyperheparinemia
Use Additional
  • code for adverse effect, if applicable, to identify drug (T45.515, T45.525)
ICD-10-CM D68.4

Acquired coagulation factor deficiency

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Deficiency of coagulation factor due to liver disease
  • Deficiency of coagulation factor due to vitamin K deficiency
Type 1 Excludes
  • vitamin K deficiency of newborn (P53)
ICD-10-CM D68.8

Other specified coagulation defects

    2016 2017 2018 2019 2020 Billable/Specific Code
Type 1 Excludes
  • hemorrhagic disease of newborn (P53)
ICD-10-CM D68.9

Coagulation defect, unspecified

    2016 2017 2018 2019 2020 Billable/Specific Code
ICD-10-CM D69.0

Allergic purpura

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Allergic vasculitis
  • Nonthrombocytopenic hemorrhagic purpura
  • Nonthrombocytopenic idiopathic purpura
  • Purpura anaphylactoid
  • Purpura Henoch(-Schönlein)
  • Purpura rheumatica
  • Vascular purpura
Type 1 Excludes
  • thrombocytopenic hemorrhagic purpura (D69.3)
ICD-10-CM D69.1

Qualitative platelet defects

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Bernard-Soulier [giant platelet] syndrome
  • Glanzmann's disease
  • Grey platelet syndrome
  • Thromboasthenia (hemorrhagic) (hereditary)
  • Thrombocytopathy
Type 1 Excludes
  • von Willebrand's disease (D68.0)
ICD-10-CM D69.2

Other nonthrombocytopenic purpura

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Purpura NOS
  • Purpura simplex
  • Senile purpura
ICD-10-CM D69.3

Immune thrombocytopenic purpura

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Hemorrhagic (thrombocytopenic) purpura
  • Idiopathic thrombocytopenic purpura
  • Tidal platelet dysgenesis
ICD-10-CM D69.41

Evans syndrome

    2016 2017 2018 2019 2020 Billable/Specific Code
ICD-10-CM D69.42

Congenital and hereditary thrombocytopenia purpura

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Congenital thrombocytopenia
  • Hereditary thrombocytopenia
Code First
  • congential or hereditary disorder, such as:
  • thrombocytopenia with absent radius (TAR syndrome) (Q87.2)
ICD-10-CM D69.49

Other primary thrombocytopenia

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Megakaryocytic hypoplasia
  • Primary thrombocytopenia NOS
ICD-10-CM D69.51

Posttransfusion purpura

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Posttransfusion purpura from whole blood (fresh) or blood products
  • PTP
ICD-10-CM D69.59

Other secondary thrombocytopenia

    2016 2017 2018 2019 2020 Billable/Specific Code
ICD-10-CM D69.6

Thrombocytopenia, unspecified

    2016 2017 2018 2019 2020 Billable/Specific Code
ICD-10-CM D69.8

Other specified hemorrhagic conditions

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Capillary fragility (hereditary)
  • Vascular pseudohemophilia
ICD-10-CM D69.9

Hemorrhagic condition, unspecified

    2016 2017 2018 2019 2020 Billable/Specific Code
ICD-10-CM D75.82

Heparin induced thrombocytopenia (HIT)

    2016 2017 2018 2019 2020 Billable/Specific Code
ICD-10-CM R23.3

Spontaneous ecchymoses

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Petechiae
Type 1 Excludes

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