On its web, CMS (Medicare) lists the proposal for ICD10 classification which should become accepted requirement in a few years.
Draft ICD-10-CM/PCS MS-DRGv26 Definitions Manual
|
D800 |
Hereditary hypogammaglobulinemia |
|
D801 |
Nonfamilial hypogammaglobulinemia |
|
D802 |
Selective deficiency of immunoglobulin A [IgA] |
|
D803 |
Selective deficiency of immunoglobulin G [IgG] subclasses |
|
D804 |
Selective deficiency of immunoglobulin M [IgM] |
|
D805 |
Immunodeficiency with increased immunoglobulin M [IgM] |
|
D807 |
Transient hypogammaglobulinemia of infancy |
|
D822 |
Immunodeficiency with short-limbed stature |
|
D823 |
Immunodeficiency following hereditary defective response to Epstein-Barr virus |
|
D824 |
Hyperimmunoglobulin E [IgE] syndrome |
|
D828 |
Immunodeficiency associated with other specified major defects |
|
D829 |
Immunodeficiency associated with major defect, unspecified |
|
D830 |
Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function |
|
D831 |
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders |
|
D832 |
Common variable immunodeficiency with autoantibodies to B- or T-cells |
|
D838 |
Other common variable immunodeficiencies |
|
D839 |
Common variable immunodeficiency, unspecified |
|
D848 |
Other specified immunodeficiencies |
|
D849 |
Immunodeficiency, unspecified |
|
D890 |
Polyclonal hypergammaglobulinemia |
|
D892 |
Hypergammaglobulinemia, unspecified |
|
D898 |
Other specified disorders involving the immune mechanism, not elsewhere classified |
|
D899 |
Disorder involving the immune mechanism, unspecified |