2020 ICD-10-CM Diagnosis Code D69.8

Other specified hemorrhagic conditions

    2016 2017 2018 2019 2020 Billable/Specific Code
  • D69.8 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
  • The 2020 edition of ICD-10-CM D69.8 became effective on October 1, 2019.
  • This is the American ICD-10-CM version of D69.8 - other international versions of ICD-10 D69.8 may differ.
Applicable To
  • Capillary fragility (hereditary)
  • Vascular pseudohemophilia
The following code(s) above D69.8 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
  • Applicable To annotations, or
  • Code Also annotations, or
  • Code First annotations, or
  • Excludes1 annotations, or
  • Excludes2 annotations, or
  • Includes annotations, or
  • Note annotations, or
  • Use Additional annotations
that may be applicable to D69.8:
  • D50-D89
    2020 ICD-10-CM Range D50-D89

    Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

    Type 2 Excludes
    • autoimmune disease (systemic) NOS (M35.9)
    • certain conditions originating in the perinatal period (P00-P96)
    • complications of pregnancy, childbirth and the puerperium (O00-O9A)
    • congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
    • endocrine, nutritional and metabolic diseases (E00-E88)
    • human immunodeficiency virus [HIV] disease (B20)
    • injury, poisoning and certain other consequences of external causes (S00-T88)
    • neoplasms (C00-D49)
    • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
    Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
  • D69
    ICD-10-CM Diagnosis Code D69

    Purpura and other hemorrhagic conditions

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • benign hypergammaglobulinemic purpura (D89.0)
    • cryoglobulinemic purpura (D89.1)
    • essential (hemorrhagic) thrombocythemia (D47.3)
    • hemorrhagic thrombocythemia (D47.3)
    • purpura fulminans (D65)
    • thrombotic thrombocytopenic purpura (M31.1)
    • Waldenström hypergammaglobulinemic purpura (D89.0)
    Purpura and other hemorrhagic conditions
Approximate Synonyms
  • Capillary fragility abnormality
Clinical Information
  • Group of hemorrhagic disorders in which the von willebrand factor is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor viii, and impaired platelet adhesion.
  • Hemophilioid disorder due to deficiency of von willebrand factor and thus of factor viii complex.
  • Hereditary or acquired coagulation disorder characterized by a qualitative or quantitative deficiency of the von willebrand factor. The latter plays an important role in platelet adhesion. Signs and symptoms include bruises, nose bleeding, gum bleeding following a dental procedure, heavy menstrual bleeding, and gastrointestinal bleeding.
  • Includes true von willebrand disease with mutation at the vwf locus, as well as mimicking disorders with other mutations (pseudo vwd) and acquired von willebrand syndrome
ICD-10-CM D69.8 is grouped within Diagnostic Related Group(s) (MS-DRG v37.0):
  • 813 Coagulation disorders

Convert D69.8 to ICD-9-CM

Code History
  • 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
  • 2017 (effective 10/1/2016): No change
  • 2018 (effective 10/1/2017): No change
  • 2019 (effective 10/1/2018): No change
  • 2020 (effective 10/1/2019): No change
Code annotations containing back-references to D69.8:
  • Type 1 Excludes: D68.0
    ICD-10-CM Diagnosis Code 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)

Diagnosis Index entries containing back-references to D69.8:
  • Endotheliosis D69.8 (hemorrhagic infectional)
  • Fragile, fragility
    • capillary D69.8 (hereditary)
  • Hemorrhage, hemorrhagic (concealed) R58
    ICD-10-CM Diagnosis Code R58

    Hemorrhage, not elsewhere classified

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Hemorrhage NOS
    Type 1 Excludes
    • hemorrhage included with underlying conditions, such as:
    • acute duodenal ulcer with hemorrhage (K26.0)
    • acute gastritis with bleeding (K29.01)
    • ulcerative enterocolitis with rectal bleeding (K51.01)
    • capillary I78.8
      ICD-10-CM Diagnosis Code I78.8

      Other diseases of capillaries

        2016 2017 2018 2019 2020 Billable/Specific Code
      • primary D69.8
    • disease D69.9
      ICD-10-CM Diagnosis Code D69.9

      Hemorrhagic condition, unspecified

        2016 2017 2018 2019 2020 Billable/Specific Code
      • specified type NEC D69.8
  • Pseudohemophilia (Bernuth's) (hereditary) (type B) D68.0
    ICD-10-CM Diagnosis Code 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)
    • Type A D69.8
    • vascular D69.8
  • Purpura D69.2
    ICD-10-CM Diagnosis Code D69.2

    Other nonthrombocytopenic purpura

      2016 2017 2018 2019 2020 Billable/Specific Code
    Applicable To
    • Purpura NOS
    • Purpura simplex
    • Senile purpura
    • capillary fragility D69.8 (hereditary) (idiopathic)

ICD-10-CM Codes Adjacent To D69.8
D69.2 Other nonthrombocytopenic purpura
D69.3 Immune thrombocytopenic purpura
D69.4 Other primary thrombocytopenia
D69.41 Evans syndrome
D69.42 Congenital and hereditary thrombocytopenia purpura
D69.49 Other primary thrombocytopenia
D69.5 Secondary 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
D70 Neutropenia
D70.0 Congenital agranulocytosis
D70.1 Agranulocytosis secondary to cancer chemotherapy
D70.2 Other drug-induced agranulocytosis
D70.3 Neutropenia due to infection
D70.4 Cyclic neutropenia
D70.8 Other neutropenia
D70.9 Neutropenia, unspecified
D71 Functional disorders of polymorphonuclear neutrophils

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.