ICD-10 · PDGM grouping
D65-D69 — Coagulation defects, purpura and other hemorrhagic conditions
Every ICD-10-CM code in this range and the PDGM clinical group CMS assigns to it, read from the CMS grouper crosswalk v07.2.26.
Codes in range
41
No clinical group
1
A period cannot be grouped from these.
Barred as primary
0
CMS rejects these in the primary position.
Where these codes group
40 of the 41 codes in D65-D69 group to MMTA - Infectious Disease, Neoplasms, and Blood-Forming Diseases. A further 1 are assigned no clinical group at all, which means a 30-day period cannot be grouped from them.
Code families in D65-D69
One page per three-character family: every code in it, whether it can lead a claim, its clinical group and comorbidity subgroup.
Every code in D65-D69
Descriptions are CMS’s own, abbreviated as CMS abbreviates them.
| Code | Description | Clinical group | Primary position |
|---|---|---|---|
| D65 | Disseminated intravascular coagulation | K | Can lead a claim |
| D66 | Hereditary factor VIII deficiency | K | Can lead a claim |
| D67 | Hereditary factor IX deficiency | K | Can lead a claim |
| D6800 | Von Willebrand disease, unspecified | K | Can lead a claim |
| D6801 | Von Willebrand disease, type 1 | K | Can lead a claim |
| D68020 | Von Willebrand disease, type 2A | K | Can lead a claim |
| D68021 | Von Willebrand disease, type 2B | K | Can lead a claim |
| D68022 | Von Willebrand disease, type 2M | K | Can lead a claim |
| D68023 | Von Willebrand disease, type 2N | K | Can lead a claim |
| D68029 | Von Willebrand disease, type 2, unspecified | K | Can lead a claim |
| D6803 | Von Willebrand disease, type 3 | K | Can lead a claim |
| D6804 | Acquired von Willebrand disease | K | Can lead a claim |
| D6809 | Other von Willebrand disease | K | Can lead a claim |
| D681 | Hereditary factor XI deficiency | K | Can lead a claim |
| D682 | Hereditary deficiency of other clotting factors | K | Can lead a claim |
| D68311 | Acquired hemophilia | K | Can lead a claim |
| D68312 | Antiphospholipid antibody with hemorrhagic disorder | K | Can lead a claim |
| D68318 | Oth hemorrhagic disord d/t intrns circ anticoag,antib,inhib | K | Can lead a claim |
| D6832 | Hemorrhagic disord d/t extrinsic circulating anticoagulants | K | Can lead a claim |
| D684 | Acquired coagulation factor deficiency | K | Can lead a claim |
| D6851 | Activated protein C resistance | K | Can lead a claim |
| D6852 | Prothrombin gene mutation | K | Can lead a claim |
| D6859 | Other primary thrombophilia | K | Can lead a claim |
| D6861 | Antiphospholipid syndrome | K | Can lead a claim |
| D6862 | Lupus anticoagulant syndrome | K | Can lead a claim |
| D6869 | Other thrombophilia | K | Can lead a claim |
| D688 | Other specified coagulation defects | K | Can lead a claim |
| D689 | Coagulation defect, unspecified | K | Can lead a claim |
| D690 | Allergic purpura | K | Can lead a claim |
| D6911 | Glanzmann thrombasthenia | K | Can lead a claim |
| D6919 | Other qualitative platelet defects | K | Can lead a claim |
| D692 | Other nonthrombocytopenic purpura | K | Can lead a claim |
| D693 | Immune thrombocytopenic purpura | K | Can lead a claim |
| D6941 | Evans syndrome | K | Can lead a claim |
| D6942 | Congenital and hereditary thrombocytopenia purpura | None | Cannot lead a claim |
| D6949 | Other primary thrombocytopenia | K | Can lead a claim |
| D6951 | Posttransfusion purpura | K | Can lead a claim |
| D6959 | Other secondary thrombocytopenia | K | Can lead a claim |
| D696 | Thrombocytopenia, unspecified | K | Can lead a claim |
| D698 | Other specified hemorrhagic conditions | K | Can lead a claim |
| D699 | Hemorrhagic condition, unspecified | K | Can lead a claim |
Source: CMS HH PPS Grouper Software v07.2.26, effective 2026-10-01. This is the crosswalk Medicare runs a claim through. Grouping also depends on admission source, timing, the OASIS functional items and the rest of the diagnosis list.
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