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D69 Purpura and other hemorrhagic conditions D69.3 Immune thrombocytopenic purpura Hemorrhagic (thrombocytopenic) purpura Idiopathic thrombocytopenic purpura Tidal platelet dysgenesis D80 Immunodeficiency with predominantly antibody defects D80.0* Hereditary hypogammaglobulinemia Autosomal recessive agammaglobulinemia (Swiss type) X-linked agammaglobulinemia [Bruton] (with growth hormone deficiency) D80.1 Nonfamilial hypogammaglobulinemia Agammaglobulinemia with immunoglobulin-bearing B-lymphocytes Common variable agammaglobulinemia [CVAgamma] Hypogammaglobulinemia NOS 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] D80.6* Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia D80.7* Transient hypogammaglobulinemia of infancy D80.8 Other immunodeficiencies with predominantly antibody defects Kappa light chain deficiency D80.9 Immunodeficiency with predominantly antibody defects, unspecified D81 Combined immunodeficiencies Excludes: autosomal recessive agammaglobulinemia (Swiss type) (D80.0) D81.0* Severe combined immunodeficiency [SCID] with reticular dysgenesis D81.1* Severe combined immunodeficiency [SCID] with low T- and B-cell numbers D81.2* Severe combined immunodeficiency [SCID] with low or normal B-cell numbers D81.31 Severe combined immunodeficiency [SCID] due to adenosine deaminase deficiency ADA deficiency with SCID Adenosine deaminase [ADA] deficiency with severe combined immunodeficiency D81.5* Purine nucleoside phosphorylase [PNP] deficiency D81.6* Major histocompatibility complex class I deficiency Bare lymphocyte syndrome D81.7* Major histocompatibility complex class II deficiency D81.82* Activated Phosphoinositide 3-kinase Delta Syndrome [APDS] p110d-activating mutation causing senescent T cells, lymphadenopathy, and immunodeficiency[PASLI] disease D81.89* Other combined immunodeficiencies D81.9* Combined immunodeficiency, unspecified Severe combined immunodeficiency disorder [SCID] NOS D82 Immunodeficiency associated with other major defects Excludes: ataxia telangiectasia [Louis-Bar] (G11.3) D82.0* Wiskott-Aldrich syndrome Immunodeficiency with thrombocytopenia and eczema D82.2 Immunodeficiency with short-limbed stature D82.3 Immunodeficiency following hereditary defective response to Epstein-Barr virus X-linked lymphoproliferative disease D82.4* Hyperimmunoglobulin E [IgE] syndrome D82.8 Immunodeficiency associated with other specified major defects D82.9 Immunodeficiency associated with major defect, unspecified D83 Common variable immunodeficiency D83.0* Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function D83.1* Common variable immunodeficiency with predominant immunoregulatory T-cell disorders D83.2* Common variable immunodeficiency with autoantibodies to B- or T-cells D83.8* Other common variable immunodeficiencies D83.9* Common variable immunodeficiency, unspecified G11.3* Cerebellar ataxia with defective DNA repair Ataxia telangiectasia [Louis-Bar] G61 Inflammatory polyneuropathy G61.81 Chronic inflammatory demyelinating polyneuritis CPT ® and HCPCS Codes (Healthcare Common Procedural Coding System) 2-5 S9338 † Home infusion therapy, immunotherapy, administrative services, professional pharmacy services, care coordination, and all necessary supplies and equipment (drugs and nursing visits coded separately), per diem J1459 Injection, immune globulin (Privigen), intravenous, non-lyophilized (eg, liquid), 500 mg Q2052 Services, supplies, and accessories used in the home for the administration of IVIg 96365 Intravenous infusion, for therapy and prophylaxis or diagnosis (specify substance or drug)
Veterinary Medicine
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