Hypergammaglobulinemia
| ICD-10 | D89.0, D89.2 |
|---|---|
| ICD-9 | 289.89 |
| MeSH | D006942 |
Hypergammaglobulinemia is a medical condition with elevated levels of gamma globulin.
It is a type of immunoproliferative disorder.
See also
| Pathology: Immune disorders (primarily D80-D89, 273, 279) | |
|---|---|
| X-linked agammaglobulinemia - Selective immunoglobulin A deficiency | |
| Combined immunodeficiencies | Severe combined immunodeficiency (X-SCID) - Adenosine deaminase deficiency - Nezelof syndrome - Purine nucleoside phosphorylase deficiency - Bare lymphocyte syndrome |
| Other | Wiskott-Aldrich syndrome - DiGeorge syndrome - Hyper-IgE syndrome - Common variable immunodeficiency - Complement deficiency (Angioedema) - Sarcoidosis - Hypergammaglobulinemia - Cryoglobulinemia - Paraproteinemia |
| Autoimmunity | see list of autoimmune diseases |
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