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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 
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 +  
epidermodysplasia verruciformis +  
erythroderma desquamativum 
familial Mediterranean fever +  
geotrichosis 
graft versus host disease +   
Granulomatosis with Polyangiitis +   
growth hormone insensitivity with immune dysregulation 1, autosomal recessive 
Histiocytic and Dendritic Cell Neoplasm +  
hyperimmunoglobulinemia D with periodic fever 
hypersensitivity reaction disease +   
An immune system disease that has basis in dysregulation of the hypersensitivity reaction, an inflammatory response to an exogenous environmental antigen or an endogenous antigen initiated by the adaptive immune system. An immune system disease that has material basis in abnormal immune responses, usually to allergens such as insect venom, dust mites, pollen, drugs or some foods.
immune deficiency disease +   
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 +   
lymphoid system disorder +   
Melkersson-Rosenthal syndrome 
multiple chemical sensitivity 
myositis +   
Neoplastic Medium-Sized B-Lymphocyte with Basophilic Cytoplasm 
phagocytic cell dysfunction +  
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 II hypersensitivity reaction disease +   
Vici syndrome 

Synonyms
Exact Synonyms: DOID:0060056 ;   NCIT:C3114 ;   allergic reaction ;   http://identifiers.org/medgen/759636 ;   http://identifiers.org/snomedct/473010000 ;   http://linkedlifedata.com/resource/umls/id/C3532523 ;   hypersensitive ;   hypersensitivity ;   hypersensitivity reaction
Broad Synonyms: sensitive ;   sensitivity
Xrefs: DOID:0060056 ;   MEDGEN:759636 ;   MONDO:0000605 ;   MP:0002148 ;   MedDRA:10020751 ;   NCI:C3114 ;   SCTID:421961002 ;   SCTID:473010000 ;   UMLS:C3532523
Definition Sources: ISBN-13:978-0-7817-3514-8

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