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. Author manuscript; available in PMC: 2013 Jun 24.
Published in final edited form as: J Clin Immunol. 2012 Sep 1;33(1):40–48. doi: 10.1007/s10875-012-9773-1

Table I.

Diagnosis, ICD codes, and numbers of PID patients

Diagnosis ICD
code
Patient
count
Percent
Hypogammaglobulinemia
unspecified
279.00 490 17.96 %
Unspecified immune deficiency 279.3 477 17.48 %
Selective deficiency IgG 279.03 274 10.04 %
DiGeorge syndrome 279.11 249 9.12 %
Common variable Immunodeficiency 279.06 242 8.87 %
Selective IgA Immunodeficiency 279.01 215 7.88 %
Single Complement Deficiency 279.8 205 7.51 %
Immunodeficiency with
predominant T-cell
defect
279.10 169 6.19 %
Unspecified disorder of immune
mechanism
279.9 147 5.39 %
Combined immunodeficiency
(includes SCID)
279.2 143 5.24 %
Selective IgM Immunodeficiency 279.02 34 1.25 %
Wiskott-Aldrich syndrome 279.12 30 1.10 %
Congenital hypogammaglobulinemia
(Agammaglobulinemia)
279.04 22 0.81 %
Transient hypogammaglobulinemia 279.09 17 0.62 %
Hyper-IgM 279.05 10 0.37 %
Autoimmune disease not elsewhere
classified
279.4 3 0.11 %
Nezelof’s syndrome 279.13 2 0.07 %
Total 2729 100.00 %