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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
22q11.2 deletion syndrome +  
acquired immunodeficiency +  
acute graft vs. host disease  
aggressive insulitis 
allergic disease +   
anaphylaxis +   
autoimmune disease +   
autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis 
autosomal dominant familial periodic fever 
autosomal recessive osteopetrosis 7 
benign insulitis 
bone marrow disorder +   
cerebral toxoplasmosis 
congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome 
congenital toxoplasmosis 
cryopyrin-associated periodic syndrome +  
drug hypersensitivity syndrome  
epidermodysplasia verruciformis +  
erythroderma desquamativum 
familial Mediterranean fever +  
geotrichosis 
graft versus host disease +   
Granulomatosis with Polyangiitis +   
growth hormone insensitivity with immune dysregulation 1, autosomal recessive 
Henoch-Schoenlein purpura  
Histiocytic and Dendritic Cell Neoplasm +  
hyperimmunoglobulinemia D with periodic fever 
hypersensitivity reaction disease +   
hypersensitivity vasculitis +  
IgE responsiveness, atopic 
immune deficiency disease +   
immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome 
immune system cancer +   
immune system organ benign neoplasm +  
immune system toxicity  
immunodeficiency disease +   
immunodeficiency-related disorder +  
immunoproliferative disorder 
infantile-onset periodic fever-panniculitis-dermatosis syndrome 
leukocyte disorder +   
lupus nephritis  
lymphoid system disorder +   
Melkersson-Rosenthal syndrome 
multiple chemical sensitivity 
myositis +   
Neoplastic Medium-Sized B-Lymphocyte with Basophilic Cytoplasm 
phagocytic cell dysfunction +  
polymyositis +   
proteosome-associated autoinflammatory syndrome +  
psoriasis +   
pyogenic arthritis-pyoderma gangrenosum-acne syndrome 
rag2 deficiency 
Rare genetic immune disease +  
Roifman syndrome 
Schnitzler syndrome 
spondyloarthropathy +   
T-cell large granular lymphocyte leukemia 
thrombocytopenic purpura +  
thymus gland disorder +  
thymus hyperplasia 
transcobalamin II deficiency 
twin-to-twin transfusion syndrome 
type 1 diabetes nephropathy  
type II hypersensitivity reaction disease +   
A disorder resulting from loss of function or tissue destruction of an organ or multiple organs, arising from humoral or cellular immune responses of the individual to their own tissue constituents. It may be systemic (e.g., systemic lupus erythematosus), or organ specific, (e.g., thyroiditis). Type II hypersenstivity disease is an immune system disease in which an abnormal inflammatory response results in disease.
type III hypersensitivity reaction disease +  
type IV hypersensitivity disease +   
Vici syndrome 

Synonyms
Exact Synonyms: DOID:417 ;   NCIT:C2889 ;   autoimmune disease ;   autoimmune disease or disorder ;   autoimmune disorder ;   http://identifiers.org/medgen/2135 ;   http://identifiers.org/mesh/D001327 ;   http://identifiers.org/snomedct/85828009 ;   http://linkedlifedata.com/resource/umls/id/C0004364 ;   https://omim.org/entry/109100
Related Synonyms: autoimmune hypersensitivity disease
Xrefs: DOID:417 ;   ICD9:279.4 ;   ICD9:279.49 ;   ICD9:720 ;   MEDGEN:2135 ;   MESH:D001327 ;   MIM:109100 ;   MONDO:0007179 ;   NCI:C2889 ;   OBI:1110054
External Ontologys: disease_arises_from_feature EFO:HP:0002960
Definition Sources: NCIT:C2889

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