Skyscape Web Viewer : International Classification of Diseases : ICD10 Index

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[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
[D81] - Combined immunodeficiencies
[D82.0]-Aldrich (-Wiskott) syndrome (eczema-thrombocytopenia)
[D82.0] - Wiskott-Aldrich syndrome
[D82.0]-Wiskott-Aldrich syndrome
[D82.1]-Alymphoplasia, thymic
[D82.1] - Di George's syndrome
[D82.1]-Di George's syndrome
[D82.1]-DiGeorge's syndrome (thymic hypoplasia)
[D82.1]-Pharyngeal pouch syndrome
[D82.2] - Immunodeficiency with short-limbed stature
[D82.3] - Immunodeficiency following hereditary defective response to Epstein-Barr virus
[D82.3]-Lymphoproliferation, X-linked disease
[D82.4] - Hyperimmunoglobulin E [IgE] syndrome
[D82.8] - Immunodeficiency associated with other specified major defects
[D82.9] - Immunodeficiency associated with major defect, unspecified
[D82] - Immunodeficiency associated with other major defects
[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
[D83] - Common variable immunodeficiency
[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