D69.42 – Congenital and hereditary thrombocytopenia purpura
ICD-10-CM 2027 diagnosis code · Coagulation defects, purpura and other hemorrhagic conditions
- Code
D69.42(claims format:D6942)- Description
- Congenital and hereditary thrombocytopenia purpura
- Billable
- Yes – valid for HIPAA-covered transactions
- Valid for
- Dates of service October 1, 2026 – September 30, 2027 (FY2027)
- Chapter
- 3. Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)
- Block
- D65-D69 Coagulation defects, purpura and other hemorrhagic conditions
- Parent codes
- D69 › D69.4
Notes for D69.42
- Congenital thrombocytopenia
- Hereditary thrombocytopenia
- congential or hereditary disorder, such as:
- thrombocytopenia with absent radius (TAR syndrome) (Q87.2)
Notes inherited from parent codes
Instructional notes at a category or block level apply to every code below it.
D69 – Purpura and other hemorrhagic conditions
D69.4 – Other primary thrombocytopenia
Index terms for D69.42
Entries in the ICD-10-CM alphabetic index that lead to this code:
Related codes in D69.4
- D69.41 – Evans syndromeBillable
- D69.49 – Other primary thrombocytopeniaBillable
Frequently asked questions
What is ICD-10 code D69.42?
D69.42 is the ICD-10-CM code for congenital and hereditary thrombocytopenia purpura, in the block D65-D69 (Coagulation defects, purpura and other hemorrhagic conditions).
Is D69.42 a billable code?
Yes. D69.42 is a billable/specific code that can be used to indicate a diagnosis for reimbursement purposes.
What category does D69.42 belong to?
It belongs to category D69 – Purpura and other hemorrhagic conditions.
Source: CDC/NCHS ICD-10-CM FY2027 code files, tabular list and index. Reference only – code assignment must follow the official ICD-10-CM guidelines and documentation in the medical record.