D80
Immunodeficiency with predominantly antibody defects
Certain disorders involving the immune mechanism (D80-D89)
Chapter 3: Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)
100 codes in this range
D80.0
Hereditary hypogammaglobulinemia
D80.1
Nonfamilial 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]
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
D80.9
Immunodeficiency with predominantly antibody defects, unspecified
D81
Combined immunodeficiencies
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
D81.3
Adenosine deaminase [ADA] deficiency
D81.30
Adenosine deaminase deficiency, unspecified
D81.31
Severe combined immunodeficiency due to adenosine deaminase deficiency
D81.32
Adenosine deaminase 2 deficiency
D81.39
Other adenosine deaminase deficiency
D81.4
Nezelof's syndrome
D81.5
Purine nucleoside phosphorylase [PNP] deficiency
D81.6
Major histocompatibility complex class I deficiency
D81.7
Major histocompatibility complex class II deficiency
D81.8
Other combined immunodeficiencies
D81.81
Biotin-dependent carboxylase deficiency
D81.810
Biotinidase deficiency
D81.818
Other biotin-dependent carboxylase deficiency
D81.819
Biotin-dependent carboxylase deficiency, unspecified
D81.82
Activated Phosphoinositide 3-kinase Delta Syndrome [APDS]
D81.89
Other combined immunodeficiencies
D81.9
Combined immunodeficiency, unspecified
D82
Immunodeficiency associated with other major defects
D82.0
Wiskott-Aldrich syndrome
D82.1
Di George's syndrome
D82.2
Immunodeficiency with short-limbed stature
D82.3
Immunodeficiency following hereditary defective response to Epstein-Barr virus
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
D84
Other immunodeficiencies
D84.0
Lymphocyte function antigen-1 [LFA-1] defect
D84.1
Defects in the complement system
D84.8
Other specified immunodeficiencies
D84.81
Immunodeficiency due to conditions classified elsewhere
D84.82
Immunodeficiency due to drugs and external causes
D84.821
Immunodeficiency due to drugs
D84.822
Immunodeficiency due to external causes
D84.89
Other immunodeficiencies
D84.9
Immunodeficiency, unspecified
D86
Sarcoidosis
D86.0
Sarcoidosis of lung
D86.1
Sarcoidosis of lymph nodes
D86.2
Sarcoidosis of lung with sarcoidosis of lymph nodes
D86.3
Sarcoidosis of skin
D86.8
Sarcoidosis of other sites
D86.81
Sarcoid meningitis
D86.82
Multiple cranial nerve palsies in sarcoidosis
D86.83
Sarcoid iridocyclitis
D86.84
Sarcoid pyelonephritis
D86.85
Sarcoid myocarditis
D86.86
Sarcoid arthropathy
D86.87
Sarcoid myositis
D86.89
Sarcoidosis of other sites
D86.9
Sarcoidosis, unspecified
D89
Other disorders involving the immune mechanism, not elsewhere classified
D89.0
Polyclonal hypergammaglobulinemia
D89.1
Cryoglobulinemia
D89.2
Hypergammaglobulinemia, unspecified
D89.3
Immune reconstitution syndrome
D89.4
Mast cell activation syndrome and related disorders
D89.40
Mast cell activation, unspecified
D89.41
Monoclonal mast cell activation syndrome
D89.42
Idiopathic mast cell activation syndrome
D89.43
Secondary mast cell activation
D89.44
Hereditary alpha tryptasemia
D89.49
Other mast cell activation disorder
D89.8
Other specified disorders involving the immune mechanism, not elsewhere classified
D89.81
Graft-versus-host disease
D89.810
Acute graft-versus-host disease
D89.811
Chronic graft-versus-host disease
D89.812
Acute on chronic graft-versus-host disease
D89.813
Graft-versus-host disease, unspecified
D89.82
Autoimmune lymphoproliferative syndrome [ALPS]
D89.83
Cytokine release syndrome
D89.831
Cytokine release syndrome, grade 1
D89.832
Cytokine release syndrome, grade 2
D89.833
Cytokine release syndrome, grade 3
D89.834
Cytokine release syndrome, grade 4
D89.835
Cytokine release syndrome, grade 5
D89.839
Cytokine release syndrome, grade unspecified
D89.84
IgG4-related disease
D89.89
Other specified disorders involving the immune mechanism, not elsewhere classified
D89.9
Disorder involving the immune mechanism, unspecified