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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Abnormal Neutrophil Chemotactic Response 
allergic disease +   
Antibody Deficiency due to Defect in CD19 
ataxia telangiectasia +   
autoimmune disease +   
An immune system disease that is an overactive immune response of the body against substances and tissues normally present in the body resulting from an abnormal functioning of the immune system that results in the production of antibodies or T cell directed against the host tissues. (DO)
Autoinflammation, Antibody Deficiency, and Immune Dysregulation, PLCG2-Associated  
Autoinflammation, Immunde Dysregulation, and Eosinophilia  
AUTOINFLAMMATORY SYNDROME, FAMILIAL, X-LINKED, BEHCET-LIKE 2  
autosomal dominant familial periodic fever  
B cell deficiency +   
C1q Deficiency  
C9 Deficiency with Dermatomyositis 
Cartilage Hair Hypoplasia Like Syndrome 
cartilage-hair hypoplasia  
Cd4+ Lymphocyte Deficiency  
CD8 Deficiency, Familial  
Chondroitin-6-Sulfaturia, Defective Cellular Immunity, Nephrotic Syndrome 
combined immunodeficiency +   
Combined Inflammatory and Immunologic Defect 
complement deficiency +   
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
Davenport Donlan Syndrome 
Deltaretrovirus Infections +   
dendritic cell deficiency +   
ectodermal dysplasia and immune deficiency +   
Endotoxin Hyporesponsiveness  
epidermodysplasia verruciformis +   
Evans Syndrome, Immunodeficiency, and Premature Immunosenescence associated with Tripeptidyl-Peptidase II Deficiency  
Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature  
familial Behcet-like autoinflammatory syndrome  
familial cold autoinflammatory syndrome +   
Familial Enteropathy with Villous Edema and Immunoglobulin G2 Deficiency 
Fanconi-like syndrome  
fetal erythroblastosis +   
Glucose-Stimulated Secretory Diarrhea, with Common Variable Immunodeficiency 
graft-versus-host disease +   
Griscelli syndrome +   
Growth Hormone Insensitivity with Immune Dysregulation +   
hepatic venoocclusive disease with immunodeficiency  
human immunodeficiency virus infectious disease +   
hypersensitivity reaction disease +   
Hypoglobulinemia and Absent B Cells 
IMAGEI Syndrome  
Immune Deficiency Disease  
Immune Deficiency, Familial Variable 
Immune Reconstitution Inflammatory Syndrome 
Immune Suppression 
immune system cancer +   
IMMUNODEFICIENCY 101 (VARICELLA ZOSTER VIRUS-SPECIFIC)  
Immunodeficiency 102  
Immunodeficiency 103  
Immunodeficiency 106  
Immunodeficiency 107  
IMMUNODEFICIENCY 15 +   
immunodeficiency 18  
immunodeficiency 20  
immunodeficiency 21  
immunodeficiency 27A  
immunodeficiency 27B  
immunodeficiency 28  
immunodeficiency 29  
immunodeficiency 31A  
immunodeficiency 31B  
immunodeficiency 31C  
immunodeficiency 35  
immunodeficiency 38  
immunodeficiency 39  
immunodeficiency 42  
immunodeficiency 43  
immunodeficiency 44  
immunodeficiency 45  
immunodeficiency 47  
immunodeficiency 51  
immunodeficiency 57  
immunodeficiency 65  
immunodeficiency 66  
Immunodeficiency 67  
Immunodeficiency 68  
Immunodeficiency 75  
Immunodeficiency 76  
Immunodeficiency 77  
Immunodeficiency 78 with Autoimmunity and Developmental Delay  
Immunodeficiency 80  
Immunodeficiency 81  
Immunodeficiency 82  
Immunodeficiency 83  
Immunodeficiency 84  
Immunodeficiency 85  
Immunodeficiency 86  
Immunodeficiency 87 and Autoimmunity  
Immunodeficiency 88  
Immunodeficiency 89 and Autoimmunity  
IMMUNODEFICIENCY 91 AND HYPERINFLAMMATION  
Immunodeficiency 92  
Immunodeficiency 93  
Immunodeficiency 94 with Autoinflammation and Dysmorphic Facies  
Immunodeficiency 95  
Immunodeficiency 96  
Immunodeficiency 97 with Autoinflammation  
Immunodeficiency 98 with Autoinflammation, X-Linked  
Immunodeficiency 99 with Hypogammaglobulinemia and Autoimmune Cytopenias  
Immunodeficiency due to Defect in MAPBP-Interacting Protein  
Immunodeficiency with Defective Leukocyte and Lymphocyte Function and with Response to Histamine-1 Antagonist 
IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA  
Immunodeficiency, Gonadal Dysgenesis, and Pulmonary Fibrosis 
immunodeficiency-centromeric instability-facial anomalies syndrome +   
immunoglobulin beta deficiency 
IMMUNOGLOBULIN KAPPA LIGHT CHAIN DEFICIENCY  
Immunoproliferative Disorders +   
Immunoskeletal Dysplasia with Neurodevelopmental Abnormalities  
INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY  
Inhibition of Lymphoblastic Transformation 
Inosine Phosphorylase Deficiency, Immune Defect Due To 
INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES  
Kotzot-Richter Syndrome 
Lichtenstein Syndrome 
Lung Damage, Immunodeficiency and Chromosome Breakage Syndrome  
lymphatic system disease +   
Lymphoblastic Transformation, Intrinsic Defect in 
Lymphokine Deficiency 
lymphopenia +   
lymphoproliferative syndrome +   
membranoproliferative glomerulonephritis +   
Monocyte Chemotactic Disorder 
Myelodysplasia, Immunodeficiency, Facial Dysmorphism, Short Stature, and Psychomotor Delay 
NEMO Mutation with Immunodeficiency 
NK cell deficiency +   
Partial Combined Immunodeficiency with Absence of HLA Determinants and Beta-2-Microglobulin from Lymphocytes 
Pelger-Huet-Like Anomaly and Episodic Fever with Abdominal Pain  
phagocyte bactericidal dysfunction +   
primary immunodeficiency disease +   
PRIMORDIAL DWARFISM-IMMUNODEFICIENCY-LIPODYSTROPHY SYNDROME  
Progressive Lymphoid System Deterioration 
Pseudo-TORCH Syndrome 2  
Pseudo-TORCH Syndrome 3  
Radiation Sensitivity of Natural Killer Activity 
Riddle syndrome  
Roifman Syndrome  
Roifman-Chitayat Syndrome  
Schimke immuno-osseous dysplasia  
sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay  
Splenic Hypoplasia  
T cell and NK cell immunodeficiency +   
T cell deficiency +   
T Cell Immunodeficiency Primary  
T-Cell OKT4 Deficiency  
Thrombocytopenic Purpura +   
Thumb Agenesis, Short Stature, and Immunodeficiency 
Transfusion Reaction +   
Transplant Rejection +   
Tuftsin Deficiency 
WHIM Syndrome +   
X-Linked Immunodeficiency with Deficiency of 115,000 Dalton Surface Glycoprotein 
 Acquired Pulmonary Alveolar Proteinosis 
 Addison's disease +   
 Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity  
 Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis +   
 antisynthetase syndrome  
 autoimmune disease of blood +   
 autoimmune disease of cardiovascular system +   
 autoimmune disease of endocrine system +   
 autoimmune disease of exocrine system +   
 autoimmune disease of gastrointestinal tract +   
 autoimmune disease of musculoskeletal system +   
 autoimmune disease of the nervous system +   
 autoimmune disease of urogenital tract +   
 Autoimmune Hypophysitis 
 autoimmune interstitial lung, joint, and kidney disease  
 autoimmune lymphoproliferative syndrome +   
 Autoimmune Progesterone Dermatitis 
 CINCA syndrome  
 Combined Immunodeficiency with Autoimmunity and Spondylometaphyseal Dysplasia  
 common variable immunodeficiency +   
 Diabetes Mellitus, Congenital Autoimmune  
 Experimental Autoimmune Uveitis +   
 familial Mediterranean fever +   
 Gardner-Diamond Syndrome 
 IgA glomerulonephritis +   
 IgG4-related disease  
 immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome  
 Immunodeficiency 78 with Autoimmunity and Developmental Delay  
 Immunodeficiency 85  
 Immunodeficiency 87 and Autoimmunity  
 Immunodeficiency 89 and Autoimmunity  
 Jaccoud's syndrome 
 Linear IgA Bullous Dermatosis 
 membranous glomerulonephritis  
 Multisystem Autoimmune Disease with Facial Dysmorphism  
 Multisystem Autoimmune Disease, Infantile-Onset +   
 Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal infections 
 Spondyloenchondrodysplasia  
 VEXAS syndrome  
 X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia  

Synonyms
Exact Synonyms: autoimmune diseases ;   autoimmune hypersensitivity disease ;   hypersensitivity reaction type II disease
Related Synonyms: AIS6 ;   Autoimmune Disease, Susceptibility To, 6 ;   autoimmune disease 6
Primary IDs: MESH:D001327
Alternate IDs: OMIM:109100 ;   OMIM:613551
Xrefs: EFO:0005140 ;   EFO:0005809 ;   ICD9CM:720
Definition Sources: http://en.wikipedia.org/wiki/Autoimmune_disease "DO" "DO"

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