D69.42 Congenital and hereditary thrombocytopenia purpura

Billable ICD-10-CM code, FY2026. Acts as a Complication or Comorbidity (CC) as a secondary diagnosis.

Applicable to

Code first

Applies from D69 Purpura and other hemorrhagic conditions

Excludes1 (never code together)

Applies from D69.4 Other primary thrombocytopenia

Excludes1 (never code together)

Risk adjustment (HCC)

MS-DRG index

Defines the logic of DRG(s) 813 in MDC 16.

Approximate ICD-9-CM (GEMs)

Code annotations containing back-references to D69.42

Back-references to D69

Diagnosis Index entries for D69.42

Nearby codes