D69.8 Other specified hemorrhagic conditions
Billable ICD-10-CM code, FY2026.
Applicable to
- Capillary fragility (hereditary)
- Vascular pseudohemophilia
Applies from D69 Purpura and other hemorrhagic conditions
Excludes1 (never code together)
- benign hypergammaglobulinemic purpura (D89.0)
- cryoglobulinemic purpura (D89.1)
- essential (hemorrhagic) thrombocythemia (D47.3)
- hemorrhagic thrombocythemia (D47.3)
- purpura fulminans (D65)
- thrombotic thrombocytopenic purpura (M31.19)
- Waldenström hypergammaglobulinemic purpura (D89.0)
Risk adjustment (HCC)
- CMS-HCC V22: HCC 48 — Coagulation Defects and Other Specified Hematological Disorders
- ESRD V24: HCC 48
MS-DRG index
Defines the logic of DRG(s) 813 in MDC 16.
Approximate ICD-9-CM (GEMs)
287.8 Other specified hemorrhagic conditions
Code annotations containing back-references to D69.8
Back-references to D69.8
- Type 1 Excludes:
D68.0 Von Willebrand disease ("capillary fragility (hereditary) (D69.8)")
Back-references to D69
- Type 1 Excludes:
R23.3 Spontaneous ecchymoses ("purpura (D69.-)")
Diagnosis Index entries for D69.8
- Endotheliosis (hemorrhagic infectional)
- Fragile, fragility › capillary (hereditary)
- Hemorrhage, hemorrhagic (concealed) › capillary › primary
- Hemorrhage, hemorrhagic (concealed) › disease › specified type NEC
- Pseudohemophilia (Bernuth's) (hereditary) (type B) › Type A
- Pseudohemophilia (Bernuth's) (hereditary) (type B) › vascular
- Purpura › capillary fragility (hereditary) (idiopathic)
Nearby codes
D69.49 Other primary thrombocytopeniaD69.5 Secondary thrombocytopeniaD69.51 Posttransfusion purpuraD69.59 Other secondary thrombocytopeniaD69.6 Thrombocytopenia, unspecifiedD69.8 Other specified hemorrhagic conditions (this code)D69.9 Hemorrhagic condition, unspecified