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ICD-10-CM Codes
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D50-D89
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D65-D69
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D69-
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2023 ICD-10-CM Diagnosis Code D69.8
2023 ICD-10-CM Diagnosis Code D69.8
Other specified hemorrhagic conditions
2016 2017 2018 2019 2020 2021 2022 2023 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 2023 edition of ICD-10-CM D69.8 became effective on October 1, 2022.
- 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:
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 v40.0):
- 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
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2023 (effective 10/1/2022): No change
Code annotations 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 2021 2022 2023 Billable/Specific Code
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 2021 2022 2023 Billable/Specific Code
- disease D69.9
ICD-10-CM Diagnosis Code D69.9
Hemorrhagic condition, unspecified
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
- Pseudohemophilia (Bernuth's) (hereditary) (type B) - see Disease, von Willebrand
- 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 2021 2022 2023 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
D69.42 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
D70.0 Congenital agranulocytosis
D70.1 Agranulocytosis secondary to cancer chemotherapy
D70.2 Other drug-induced agranulocytosis
D70.3 Neutropenia due to infection
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.