Immunodeficient Conditions (1068)    NLM VALUE SETS (802.2)

Severe combined immunodeficiency due to absent peripheral T cell maturation 
(disorder)

Severe combined immunodeficiency disease (disorder)

Human immunodeficiency virus-related gut disease - cause unknown (disorder)

Metaphyseal chondrodysplasia, McKusick type with associated immunodeficiency 
(disorder)

Human immunodeficiency virus infection with aseptic meningitis (disorder)

De Vaal's syndrome (disorder)

Acquired immunodeficiency syndrome with dermatomycosis (disorder)

Autosomal recessive severe combined immunodeficiency disease (disorder)

Congenital immunodeficiency involving the hematopoietic system (disorder)

Chronic granulomatous disease (disorder)

Human immunodeficiency virus encephalitis (disorder)

Immunodeficiency with multicarboxylase deficiency (disorder)

Secondary immune deficiency disorder (disorder)

B-lymphocyte immunodeficiency (disorder)

T-lymphocyte immunodeficiency (disorder)

Oral hairy leukoplakia associated with immunodeficiency (disorder)

Oral hairy leukoplakia associated with human immunodeficiency virus disease 
(disorder)

Human immunodeficiency virus seroconversion exanthem (disorder)

X-linked hyper-immunoglobulin M syndrome (disorder)

Hairy leukoplakia of tongue associated with human immunodeficiency virus 
disease (disorder)

Leukoplakia of tongue associated with human immunodeficiency virus disease 
(disorder)

Candidiasis of lung associated with acquired immunodeficiency syndrome 
(disorder)

Smoldering chronic lymphocytic leukemia (disorder)

Wiskott-Aldrich syndrome (disorder)

Hepatitis B associated with Human immunodeficiency virus infection (disorder)

Combined immunodeficiency disease (disorder)

Non-Hodgkin lymphoma associated with Human immunodeficiency virus infection 
(disorder)

Infectious disease associated with acquired immune deficiency syndrome 
(disorder)

Symptomatic human immunodeficiency virus infection (disorder)

Congenital immunodeficiency disease (disorder)

Severe combined immunodeficiency due to absent adenosine deaminase (disorder)

Hypopigmentation-immunodeficiency disease (disorder)

Chronic granulomatous disease, type IA (disorder)

Human immunodeficiency virus I infection (disorder)

Severe combined immunodeficiency due to absent interleukin-2 production 
(disorder)

Human immunodeficiency virus infection with infectious mononucleosis-like 
syndrome (disorder)

Human immunodeficiency virus infection with infection by another virus 
(disorder)

Severe combined immunodeficiency due to absent T cell receptor (disorder)

Congenital human immunodeficiency virus infection (disorder)

Primary immune deficiency disorder (disorder)

Acquired immunodeficiency syndrome-like syndrome (disorder)

Acquired immune deficiency syndrome (disorder)

X-linked agammaglobulinemia (disorder)

Severe combined immunodeficiency due to absent class II human leukocyte 
antigens (disorder)

Chronic granulomatous tuberculosis (disorder)

Chronic granulomatous disease, type IVA (disorder)

Acquired immunodeficiency syndrome with Salmonella infection (disorder)

Immunodeficiency with thymoma (disorder)

DiGeorge sequence (disorder)

Chronic granulomatous disease, type II (disorder)

Positive serological AND/OR viral culture findings for human immunodeficiency 
virus (disorder)

Human immunodeficiency virus II infection (disorder)

Hyperimmunoglobulin M syndrome (disorder)

Chronic granulomatous disease, type III (disorder)

Human immunodeficiency virus infection (disorder)

Human immunodeficiency virus infection with acute lymphadenitis (disorder)

Acquired immunodeficiency syndrome virus infection associated with pregnancy 
(disorder)

Asymptomatic human immunodeficiency virus infection (disorder)

Chronic granulomatous disease, type IV (disorder)

Asymptomatic human immunodeficiency virus infection in pregnancy (disorder)

Chronic lymphoid leukemia, disease (disorder)

Granulomatous meningoencephalitis (disorder)

Persistent generalized lymphadenopathy (disorder)

Immunodeficiency secondary to neoplasm (disorder)

Immunodeficiency secondary to trauma (disorder)

Immunodeficiency secondary to corticosteroids (disorder)

Immunodeficiency secondary to radiation therapy (disorder)

Immunodeficiency secondary to chemotherapy (disorder)

Reticular dysgenesis (disorder)

Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)

Severe combined immunodeficiency due to absent interleukin-2 receptor (disorder)

Acute human immunodeficiency virus infection (disorder)

Human immunodeficiency virus infection constitutional disease (disorder)

Human immunodeficiency virus infection with neurological disease (disorder)

Human immunodeficiency virus infection with secondary clinical infectious 
disease (disorder)

Human immunodeficiency virus with secondary cancers (disorder)

Human immunodeficiency virus disease resulting in mycobacterial infection 
(disorder)

Human immunodeficiency virus disease resulting in cytomegaloviral disease 
(disorder)

Human immunodeficiency virus disease resulting in candidiasis (disorder)

Human immunodeficiency virus disease resulting in multiple infections (disorder)

Common variable agammaglobulinemia (disorder)

Human immunodeficiency virus disease resulting in Burkitt's lymphoma (disorder)

Human immunodeficiency virus disease resulting in multiple malignant neoplasms 
(disorder)

Human immunodeficiency virus disease resulting in lymphoid interstitial 
pneumonitis (disorder)

Selective immunoglobulin A deficiency (disorder)

Selective immunoglobulin M deficiency (disorder)

Selective immunoglobulin G deficiency (disorder)

Autosomal recessive severe combined immunodeficiency (disorder)

Thymic aplasia or dysplasia with immunodeficiency (disorder)

Severe combined immunodeficiency with low T- and B-cell numbers (disorder)

Severe combined immunodeficiency with low or normal B-cell numbers (disorder)

Lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome (disorder)

Immunodeficiency following hereditary defective response to Epstein-Barr 
virus (disorder)

Common variable immunodeficiency with predominant abnormalities of B-cell 
numbers and functions (disorder)

Common variable immunodeficiency with predominant immunoregulatory T-cell 
disorders (disorder)

Common variable immunodeficiency with autoantibodies to B- or T-cells (disorder)

X-linked severe combined immunodeficiency (disorder)

Human immunodeficiency virus leukoencephalopathy (disorder)

Human immunodeficiency virus myelitis (disorder)

Immunodeficiency disorder (disorder)

X-linked agammaglobulinemia with growth hormone deficiency (disorder)

Severe combined immunodeficiency with maternofetal engraftment (disorder)

Chronic granulomatous disease, type IIA (disorder)

Benign combined immunodeficiency (disorder)

Immunodeficiency with major anomalies (disorder)

Immunodeficiency associated with chromosomal abnormality (disorder)

Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency 
(disorder)

Microcephaly, normal intelligence and immunodeficiency (disorder)

Immunodeficiency associated with multiple organ system abnormalities (disorder)

Age-related immunodeficiency (disorder)

Drug-induced immunodeficiency (disorder)

Chronic gingival granulomatous condition (disorder)

Human immunodeficiency virus-associated periodontitis (disorder)

Chronic granulomatous disease, type I (disorder)

Chronic granulomatous gastritis (disorder)

Human immunodeficiency virus enteropathy (disorder)

Acquired immune deficiency syndrome-related nephropathy (disorder)

Human immunodeficiency virus myopathy (disorder)

Acquired immune deficiency syndrome-related complex (disorder)

Chronic granulomatous infection due mostly to Staphylococcus aureus (disorder)

Congenital acquired immune deficiency syndrome (disorder)

Congenital human immunodeficiency virus positive status syndrome (disorder)

Chronic lymphocytic prolymphocytic leukemia syndrome (disorder)

Human immunodeficiency virus-related sclerosing cholangitis (disorder)

Chronic lymphoid leukemia, in remission

Nezelof's syndrome

Other deficiency of cell-mediated immunity

Combined immunity deficiency

Unspecified immunity deficiency

Nonspecific serologic evidence of human immunodeficiency virus [HIV]

Human immunodeficiency virus [HIV] disease

Human immunodeficiency virus, type 2 [HIV-2]

Chronic lymphoid leukemia, without mention of having achieved remission

Hypogammaglobulinemia, unspecified

Immunodeficiency with predominant T-cell defect, unspecified

Chronic lymphoid leukemia, in relapse

Contact with or exposure to other viral diseases

Asymptomatic human immunodeficiency virus [HIV] infection status

Kidney replaced by transplant

Heart replaced by transplant

Heart valve replaced by transplant

Skin replaced by transplant

Bone replaced by transplant

Cornea replaced by transplant

Lung replaced by transplant

Liver replaced by transplant

Selective IgA immunodeficiency

Bone marrow replaced by transplant

Peripheral stem cells replaced by transplant

Pancreas replaced by transplant

Organ or tissue replaced by transplant, intestines

Other specified organ or tissue replaced by transplant

Unspecified organ or tissue replaced by transplant

Selective IgM immunodeficiency

Immunodeficiency with increased IgM

Common variable immunodeficiency

Other deficiency of humoral immunity

Digeorge's syndrome

Wiskott-aldrich syndrome

Human immunodeficiency virus [HIV] disease

Severe combined immunodeficiency [SCID] with low T- and B-cell numbers

Severe combined immunodeficiency [SCID] with low or normal B-cell numbers

Nezelof's syndrome

Major histocompatibility complex class I deficiency

Major histocompatibility complex class II deficiency

Other combined immunodeficiencies

Combined immunodeficiency, unspecified

Wiskott-Aldrich syndrome

Di George's syndrome

Immunodeficiency with short-limbed stature

Human immunodeficiency virus, type 2 [HIV 2] as the cause of diseases classified 
elsewhere

Immunodeficiency following hereditary defective response to Epstein-Barr virus

Common variable immunodeficiency with predominant abnormalities of B-cell 
numbers and function

Common variable immunodeficiency with predominant immunoregulatory T-cell 
disorders

Common variable immunodeficiency with autoantibodies to B- or T-cells

Other common variable immunodeficiencies

Common variable immunodeficiency, unspecified

Other specified immunodeficiencies

Immunodeficiency, unspecified

Granulomatous hepatitis, not elsewhere classified

Other granulomatous disorders of the skin and subcutaneous tissue

Chronic lymphocytic leukemia of B-cell type not having achieved remission

Granulomatous disorder of the skin and subcutaneous tissue, unspecified

Granulomatous prostatitis

Kidney transplant status

Heart transplant status

Lung transplant status

Heart and lungs transplant status

Liver transplant status

Skin transplant status

Bone transplant status

Corneal transplant status

Chronic lymphocytic leukemia of B-cell type in relapse

Bone marrow transplant status

Pancreas transplant status

Stem cells transplant status

Nonfamilial hypogammaglobulinemia

Selective deficiency of immunoglobulin A [IgA]

Selective deficiency of immunoglobulin M [IgM]

Immunodeficiency with increased immunoglobulin M [IgM]

Severe combined immunodeficiency [SCID] with reticular dysgenesis