VITiếng Việt
ICD-10 Vietnam

D80-D89

Certain disorders involving the immune mechanism

D80 Immunodeficiency with predominantly antibody defects D80.0 Primary diagnosis candidate Hereditary hypogammaglobuli naemia D80.1 Primary diagnosis candidate Nonfamilial hypogammaglobuli naemia D80.2 Primary diagnosis candidate Selective deficiency of immunoglobulin A [IgA] D80.3 Primary diagnosis candidate Selective deficiency of immunoglobulin G [IgG] subclasses D80.4 Primary diagnosis candidate Selective deficiency of immunoglobulin M [IgM] D80.5 Primary diagnosis candidate Immunodeficiency with increased immunoglobulin M [IgM] D80.6 Primary diagnosis candidate Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobul inaemia D80.7 Primary diagnosis candidate Transient hypogammaglobuli naemia of infancy D80.8 Primary diagnosis candidate Other immunodeficiencies with predominantly antibody defects D80.9 Primary diagnosis candidate Immunodeficiency with predominantly antibody defects, unspecified D81 Combined immunodeficiencies D81.0 Primary diagnosis candidate Severe combined immunodeficiency [SCID] with reticular dysgenesis D81.1 Primary diagnosis candidate Severe combined immunodeficiency [SCID] with low T- and B-cell numbers D81.2 Primary diagnosis candidate Severe combined immunodeficiency [SCID] with low or normal B-cell numbers D81.3 Primary diagnosis candidate Adenosine deaminase [ADA] deficiency D81.4 Primary diagnosis candidate Nezelof syndrome D81.5 Primary diagnosis candidate Purine nucleoside phosphorylase [PNP] deficiency D81.6 Primary diagnosis candidate Major histocompatibility complex class I deficiency D81.7 Primary diagnosis candidate Major histocompatibility complex class II deficiency D81.8 Primary diagnosis candidate Other combined immunodeficiencies D81.9 Primary diagnosis candidate Combined immunodeficiency, unspecified D82 Immunodeficiency associated with other major defects D82.0 Primary diagnosis candidate Wiskott-Aldrich syndrome D82.1 Primary diagnosis candidate Di George syndrome D82.2 Primary diagnosis candidate Immunodeficiency with short-limbed stature D82.3 Primary diagnosis candidate Immunodeficiency following hereditary defective response to Epstein-Barr virus D82.4 Primary diagnosis candidate Hyperimmunoglobu lin E [IgE] syndrome D82.8 Primary diagnosis candidate Immunodeficiency associated with other specified major defects D82.9 Primary diagnosis candidate Immunodeficiency associated with major defect, unspecified D83 Common variable immunodeficiency D83.0 Primary diagnosis candidate Common variable immunodeficiency with predominant abnormalities of B- cell numbers and function D83.1 Primary diagnosis candidate Common variable immunodeficiency with predominant immunoregulatory T-cell disorders D83.2 Primary diagnosis candidate Common variable immunodeficiency with autoantibodies to B- or T-cells D83.8 Primary diagnosis candidate Other common variable immunodeficiencies D83.9 Primary diagnosis candidate Common variable immunodeficiency, unspecified D84 Other immunodeficiencies D84.0 Primary diagnosis candidate Lymphocyte function antigen-1 [LFA-1] defect D84.1 Primary diagnosis candidate Defects in the complement system D84.8 Primary diagnosis candidate Other specified immunodeficiencies D84.9 Primary diagnosis candidate Immunodeficiency, unspecified D86 Sarcoidosis D86.0 Primary diagnosis candidate Sarcoidosis of lung D86.1 Primary diagnosis candidate Sarcoidosis of lymph nodes D86.2 Primary diagnosis candidate Sarcoidosis of lung with sarcoidosis of lymph nodes D86.3 Primary diagnosis candidate Sarcoidosis of skin D86.8 Primary diagnosis candidate Sarcoidosis of other and combined sites D86.9 Primary diagnosis candidate Sarcoidosis, unspecified D89 Other disorders involving the immune mechanism, not elsewhere classified D89.0 Primary diagnosis candidate Polyclonal hypergammaglobuli naemia