HCC 115 (V28)
Specified Immunodeficiencies and White Blood Cell Disorders
19 ICD-10-CM codes map to this category in the CMS-HCC V28 risk adjustment model for payment year 2027. All 115 HCCs
Overridden by: HCC 114 (Common Variable and Combined Immunodeficiencies). If the patient also has one of these, only the higher HCC counts.
| D70.0 | Congenital agranulocytosis |
| D70.4 | Cyclic neutropenia |
| D71 | Functional disorders of polymorphonuclear neutrophils |
| D71.1 | Leukocyte adhesion deficiency |
| D71.8 | Other functional disorders of polymorphonuclear neutrophils |
| D71.9 | Functional disorders of polymorphonuclear neutrophils, unspecified |
| D72.0 | Genetic anomalies of leukocytes |
| D76.1 | Hemophagocytic lymphohistiocytosis |
| D76.3 | Other histiocytosis syndromes |
| D80.0 | Hereditary hypogammaglobulinemia |
| D80.2 | Selective deficiency of immunoglobulin A [IgA] |
| D80.3 | Selective deficiency of immunoglobulin G [IgG] subclasses |
| D80.4 | Selective deficiency of immunoglobulin M [IgM] |
| D80.5 | Immunodeficiency with increased immunoglobulin M [IgM] |
| D81.4 | Nezelof's syndrome |
| D82.0 | Wiskott-Aldrich syndrome |
| D82.1 | Di George's syndrome |
| D84.1 | Defects in the complement system |
| D89.84 | IgG4-related disease |
