Structure of immune system
Immune system structure
Immune system structure (body structure)
Structure of immune system (body structure)
Immune system
116003000
http://purl.bioontology.org/ontology/SNOMEDCT/116003000
0
XU9ED
Immune system diagnostic imaging procedure
Immune system measurement of physiology/function
Immune system repair
Immune system surgical procedure
Immune system destructive procedure
Immune system incision
Surgical implantation to lymphatic system
Immune system excision
Immune system evaluation
Biopsy of immune system structure
Site specific immune system surgical procedure
Immune system physical examination
Immune system endoscopy
Major histocompatibility complex class II deficiency
Lymphocyte function antigen-1 defect
De Vaal's syndrome
Defective phagocytic cell opsonization
Defective phagocytic cell chemotaxis
Infectious disorder of immune system
Graft versus host reaction
Reticular dysgenesis
Factor D deficiency
Inflammatory disorder of immune system
Complement 1q dysfunction
Homologous restriction factor deficiency
Transient immunodeficiency of infancy
Immunoglobulin A1 deficiency
X-linked agammaglobulinemia with growth hormone deficiency
Properdin deficiency disease
Severe combined immunodeficiency with low or normal B-cell numbers
Immunoglobulin G4 deficiency
Familial hemophagocytic lymphohistiocytosis
Complement 8 beta chain deficiency
Congenital hypogammaglobulinemia
Selective immunoglobulin E deficiency
Disorder of immune structure
Hereditary angioneurotic edema
Hyperimmunoglobulin D with periodic fever
Specific antibody deficiency
Complement 3 deficiency
Factor I deficiency
Deletion of X-chromosome and hypogammaglobulinemia
Hereditary C1 esterase inhibitor deficiency - deficient factor
Lambda light chain deficiency
Defective phagocytic cell adhesion
Anti-staphylococcal antibody deficiency
Complement 1r deficiency
Mannan-binding protein deficiency
Feline infectious peritonitis
Terminal component deficiency
Complement 5a inhibitor deficiency
AIDS with dermatomycosis
Acquired C1 esterase inhibitor deficiency
Severe combined immunodeficiency with maternofetal engraftment
Autosomal agammaglobulinemia with absent B-cells
Immunoglobulin A2 deficiency
Immunodeficiency following hereditary defective response to Epstein-Barr virus
Agammaglobulinemia
Hereditary angioneurotic edema with normal C1 esterase inhibitor activity
Complement 8 beta chain dysfunction
CD4 T lymphocyte deficiency
Polyclonal hypergammaglobulinemia
Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency
Kappa light chain deficiency
Deficiencies of humoral immunity
Selective immunoglobulin D deficiency
Congenital dysphagocytosis
Classical complement pathway abnormality
Chronic disease of immune structure
Anti-polysaccharide antibody deficiency
Immunoglobulin heavy chain deficiency
Traumatic injury of immune system
Factor H deficiency
Alternative pathway deficiency
Microcephaly, normal intelligence and immunodeficiency
Lazy leukocyte syndrome
Hypoalphaglobulinemia
Feline infectious peritonitis AND pleuritis
Primary immunoglobulin catabolism abnormality
Leukocyte adhesion deficiency - type 1
Immunoglobulin G2 deficiency
Complement 1s deficiency
Complement 6 deficiency
Anaphylotoxin inactivator deficiency
Drug-induced immunodeficiency
Complement 5 deficiency
Hemolytic erythrophagocytic syndrome
Effusive feline infectious peritonitis
Hypopigmentation-immunodeficiency disease
Immunoglobulin-associated molecule deficiency
Selective immunoglobulin dysfunction
Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions
Other disorder of immune system associated with AIDS
Warts, hypogammaglobulinemia, infections, and myelokathexis
Wiskott-Aldrich autosomal dominant variant syndrome
Complement 4 deficiency
Complement 8 alpha-gamma deficiency
Chromosome 18 syndromes and antibody deficiency
AIDS
Selective immunoglobulin M and immunoglobulin A deficiency
Anti-meningococcal polysaccharide A antibody deficiency
Functional disorders of polymorphonuclear neutrophils
Anti-haemophilus influenzae B polysaccharide antibody deficiency
Complement 1q deficiency
Complement 4 binding protein deficiency
Hypobetaglobulinemia
Wiskott-Aldrich syndrome
Cellular immune defect
Factor B deficiency
Immunodeficiency associated with multiple organ system abnormalities
Selective immunoglobulin M deficiency
X-linked lymphoproliferative syndrome
Triple X syndrome, epilepsy, and hypogammaglobulinemia
Chédiak-Higashi syndrome
Severe combined immunodefiency with reticular dysgenesis
Immunoglobulin hypercatabolism
Combined immunoglobulin G2 and G4 deficiency
Complement 7 deficiency
Leukocyte adhesion deficiency - type 2
T-lymphocyte deficiency
Complement 2 deficiency
Complement receptor 3 deficiency
Reactive immunoproliferative disease
Complement receptor deficiency
Noneffusive feline infectious peritonitis
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
Benign combined immunodeficiency
Gluthathione peroxidase deficiency
Secretory piece deficiency
X-linked hyperimmunoglobulin M syndrome
Complement 4A deficiency
Predominantly T-cell defect
Neutrophil secondary granule deficiency
Immunodeficiency secondary to corticosteroids
Chromosome 22 abnormalities with hypogammaglobulinemia
AIDS with Salmonella infection
Complement 9 deficiency
Major histocompatibility complex class I deficiency
Immunoglobulin light chain deficiency
Reticular dysgenesis with congenital aleukocytosis
Anti-pneumococcal polysaccharide antibody deficiency
Immune system complication of procedure
Myeloperoxidase deficiency
Anti-meningococcal polysaccharide C antibody deficiency
Lipochrome histiocytosis - familial
Complement 1q beta chain deficiency
Age-related immunodeficiency
Decay accelerating factor deficiency
Immunoproliferative small intestinal disease (clinical)
Congenital leukocyte adherence deficiency
Immunoglobulinemia with isolated somatotropin deficiency
Selective immunoglobulin G deficiency
Immunoglobulin G1 deficiency
Severe combined immunodeficiency with low T- and B-cell numbers
Selective immunoglobulin A deficiency
Humoral immune defect
Tuftsin deficiency
Familial immunoglobulin hypercatabolism
Immunoglobulin G3 deficiency
Combined complement 6 and 7 deficiencies
Immunodeficiency with major anomalies
Complement receptor 1 deficiency
Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
Autosomal recessive hyperimmunoglobulin M syndrome
Common variable immunodeficiency with autoantibodies to B- or T-cells
Combined phagocytic defect
Defective immunoglobulin glycosylation
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor
Complement 4B deficiency
Complement regulatory factor defect
Gluthathione synthetase deficiency
Complement 5 dysfunction
Immunoglobulin G subclass deficiency
Monosomy 22 and absence of immunoglobulin A
Familial C3B inhibitor deficiency syndrome
Anti-protein antibody deficiency
Immune system transplantation
Body system structure
1
Entire body as a whole
In vivo immunologic procedure
Immune system procedure by site
Procedure on immune system
Body System
T-C0103
T022
C0020962
Immunologic cell
Forbidden clone
Secretory macrophage
Armed macrophage
Hybridoma
Helper cell
Fat-laden macrophage
Alveolar macrophage
Abnormal macrophage
Macrophage
Clone
Immune effector cell
Hemosiderin-laden macrophage
loading...