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 Term

Congenital thrombocytopenia
Hereditary thrombocytopenia

codefirst

congential or hereditary disorder, such as:
thrombocytopenia with absent radius (TAR syndrome) (Q87.2)

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

hereditary icd 10

thrombocytopenia icd 10

congenital icd 10

Billable/Specific Code

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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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