D69.42 - Congenital and hereditary thrombocytopenia purpura
- Applicable to Congenital and hereditary thrombocytopenia purpura
- The 2025 edition of ICD10-CM D69.42 became effective on October 1, 2024.
- This is the American ICD10-CM version of D69.42 - other international versions of ICD10 D69.42 may differ.
- D69.42 is a Billable / Specific ICD10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
Inclusion terms help to clarify and specify the conditions or diseases covered by a particular ICD-10-CM code.
Inclusion Term:
- Congenital thrombocytopenia
- Hereditary thrombocytopenia
codefirst
- congential or hereditary disorder, such as:
- thrombocytopenia with absent radius (TAR syndrome) (Q87.2)
Billable/Specific Code
The following codes above D69.42 contain annotation back-references that may be applicable to D69.42:
- Chapter: D50-D89 - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
- Section: D65-D69 - Coagulation defects, purpura and other hemorrhagic conditions
- Category: D69 - Purpura and other hemorrhagic conditions
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Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
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