D70-D77 — Other disorders of blood and blood-forming organs
Every ICD-10-CM code in this range and the PDGM clinical group CMS assigns to it, read from the CMS grouper crosswalk v07.1.26.
Codes in range
61
No clinical group
5
A period cannot be grouped from these.
Barred as primary
0
CMS rejects these in the primary position.
Where these codes group
56 of the 61 codes in D70-D77 group to MMTA - Infectious Disease, Neoplasms, and Blood-Forming Diseases. A further 5 are assigned no clinical group at all, which means a 30-day period cannot be grouped from them.
Every code in D70-D77
Descriptions are CMS’s own, abbreviated as CMS abbreviates them.
| Code | Description | Clinical group | Primary position |
|---|---|---|---|
| D700 | Congenital agranulocytosis | K | Accepted |
| D701 | Agranulocytosis secondary to cancer chemotherapy | K | Accepted |
| D702 | Other drug-induced agranulocytosis | K | Accepted |
| D703 | Neutropenia due to infection | K | Accepted |
| D704 | Cyclic neutropenia | K | Accepted |
| D708 | Other neutropenia | K | Accepted |
| D709 | Neutropenia, unspecified | K | Accepted |
| D711 | Leukocyte adhesion deficiency | K | Accepted |
| D718 | Other functional disorders of polymorphonuclear neutrophils | K | Accepted |
| D719 | Functional disorders of polymorphonuclear neutrophils, unsp | K | Accepted |
| D720 | Genetic anomalies of leukocytes | K | Accepted |
| D7210 | Eosinophilia, unspecified | K | Accepted |
| D72110 | Idiopathic hypereosinophilic syndrome [IHES] | K | Accepted |
| D72111 | Lymphocytic Variant Hypereosinophilic Syndrome [LHES] | K | Accepted |
| D72118 | Other hypereosinophilic syndrome | K | Accepted |
| D72119 | Hypereosinophilic syndrome [HES], unspecified | K | Accepted |
| D7212 | Drug rash with eosinophilia and systemic symptoms syndrome | K | Accepted |
| D7218 | Eosinophilia in diseases classified elsewhere | None | Cannot group |
| D7219 | Other eosinophilia | K | Accepted |
| D72810 | Lymphocytopenia | K | Accepted |
| D72818 | Other decreased white blood cell count | K | Accepted |
| D72819 | Decreased white blood cell count, unspecified | K | Accepted |
| D72820 | Lymphocytosis (symptomatic) | K | Accepted |
| D72821 | Monocytosis (symptomatic) | K | Accepted |
| D72822 | Plasmacytosis | K | Accepted |
| D72823 | Leukemoid reaction | K | Accepted |
| D72824 | Basophilia | K | Accepted |
| D72825 | Bandemia | K | Accepted |
| D72828 | Other elevated white blood cell count | K | Accepted |
| D72829 | Elevated white blood cell count, unspecified | K | Accepted |
| D7289 | Other specified disorders of white blood cells | K | Accepted |
| D729 | Disorder of white blood cells, unspecified | K | Accepted |
| D730 | Hyposplenism | K | Accepted |
| D731 | Hypersplenism | K | Accepted |
| D732 | Chronic congestive splenomegaly | K | Accepted |
| D733 | Abscess of spleen | K | Accepted |
| D734 | Cyst of spleen | K | Accepted |
| D735 | Infarction of spleen | K | Accepted |
| D7381 | Neutropenic splenomegaly | K | Accepted |
| D7389 | Other diseases of spleen | K | Accepted |
| D739 | Disease of spleen, unspecified | None | Cannot group |
| D740 | Congenital methemoglobinemia | K | Accepted |
| D748 | Other methemoglobinemias | K | Accepted |
| D749 | Methemoglobinemia, unspecified | K | Accepted |
| D750 | Familial erythrocytosis | K | Accepted |
| D751 | Secondary polycythemia | K | Accepted |
| D7581 | Myelofibrosis | None | Cannot group |
| D75821 | Non-immune heparin-induced thrombocytopenia | K | Accepted |
| D75822 | Immune-mediated heparin-induced thrombocytopenia | K | Accepted |
| D75828 | Other heparin-induced thrombocytopenia syndrome | K | Accepted |
| D75829 | Heparin-induced thrombocytopenia, unspecified | K | Accepted |
| D75838 | Other thrombocytosis | K | Accepted |
| D75839 | Thrombocytosis, unspecified | K | Accepted |
| D7584 | Other platelet-activating anti-PF4 disorders | K | Accepted |
| D7589 | Other specified diseases of blood and blood-forming organs | K | Accepted |
| D759 | Disease of blood and blood-forming organs, unspecified | None | Cannot group |
| D75A | Glucose-6-phosphate dehydrgnse (G6PD) defic without anemia | K | Accepted |
| D761 | Hemophagocytic lymphohistiocytosis | K | Accepted |
| D762 | Hemophagocytic syndrome, infection-associated | K | Accepted |
| D763 | Other histiocytosis syndromes | K | Accepted |
| D77 | Oth disord of bld/bld-frm organs in diseases classd elswhr | None | Cannot group |
Source: CMS HH PPS Grouper Software v07.1.26, effective 2026-04-01. 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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