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Term:
Parent Terms Term With Siblings Child Terms
Abnormal Neutrophil Chemotactic Response 
allergic disease +   
Anhidrotic Ectodermal Dysplasia with T-Cell Immunodeficiency, Autosomal Dominant  
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  
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 +   
Endotoxin Hyporesponsiveness  
epidermodysplasia verruciformis +   
Evans Syndrome, Immunodeficiency, and Premature Immunosenescence associated with Tripeptidyl-Peptidase II Deficiency  
Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature  
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 vs 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 Response to Synthetic Polypeptide--IrGAT 
Immune Suppression 
immune system cancer +   
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 due to Defect in MAPBP-Interacting Protein  
Immunodeficiency due to Ficolin 3 Deficiency  
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  
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, Inhibition of 
Lymphoblastic Transformation, Intrinsic Defect in 
Lymphoid System Deterioration, Progressive 
Lymphokine Deficiency 
lymphopenia +   
lymphoproliferative syndrome +   
MASP2 Deficiency  
membranoproliferative glomerulonephritis +   
Monocyte Chemotactic Disorder 
Myelodysplasia, Immunodeficiency, Facial Dysmorphism, Short Stature, and Psychomotor Delay 
NEMO Mutation with Immunodeficiency 
NK cell deficiency +   
otulipenia  
Partial Combined Immunodeficiency with Absence of HLA Determinants and Beta-2-Microglobulin from Lymphocytes 
phagocyte bactericidal dysfunction +   
primary immunodeficiency disease +   
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 

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: ICD9CM:720
Definition Sources: http://en.wikipedia.org/wiki/Autoimmune_disease "DO"

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.