Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)

Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
disease +     
acute disease +   
animal disease +  
breast disease +   
cancer or benign tumor +   
cardiovascular disease +   
chromosomal disorder +  
chronic disease +   
complication +   
connective tissue disease +   
digestive system disease +   
disease related to transplantation +   
disorder of development or morphogenesis +   
disorder of visual system +   
endocrine system disease +   
genetic disorder +   
head and neck disorder +   
hematologic disease +   
iatrogenic disease +  
idiopathic disease +   
immune system disease +   
A disorder resulting from an abnormality in the immune system. A group of non-neoplastic and neoplastic disorders resulting from the deregulation and/or deficiency of immune system functions. It includes autoimmune disorders (e.g., lupus erythematosus, dermatomyositis, rheumatoid arthritis), congenital and acquired immunodeficiency syndromes including the acquired immune deficiency syndrome (AIDS), and neoplasms (e.g., lymphomas and malignancies secondary to transplantation.)
infectious disease +   
inflammatory disease +   
integumentary system disease +   
metabolic disease +   
mitochondrial disease +  
musculoskeletal system disease +   
nervous system disease +   
obstetric disorder +   
occupational disorder +   
otorhinolaryngologic disease +   
perinatal disease +   
perineum disease 
poisoning +   
post-infectious disorder +   
premature aging syndrome +   
psychiatric disorder +   
radiation-induced disorder +   
reproductive system disease +   
respiratory system disease +   
soft tissue disease  
sudden infant death syndrome +  
syndromic disease +   
ulcer disease +   
upper digestive tract disorder +   
urinary system disease +   
urogenital neoplasm +   
 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 +   
 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: AUTOIMMUNE DISEASE NEC ;   Autoimmune disease, not elsewhere classified ;   DEFIC CELL IMMUNITY NOS ;   DOID:2914 ;   Deficiency of cell-mediated immunity ;   Disorder of the immune mechanism NOS ;   Disorder of the immune mechanism NOS (disorder) ;   Disorders involving the immune mechanism ;   IMMUNDEF T-CELL DEF NOS ;   IMMUNE MECHANISM DIS NEC
Xrefs: DOID:2914 ;   HP:0002715 ;   ICD10:D89 ;   ICD9:279 ;   ICD9:279.1 ;   ICD9:279.10 ;   ICD9:279.19 ;   ICD9:279.4 ;   ICD9:279.49 ;   ICD9:279.8
External Ontologys: disease_has_location EFO:UBERON:0002405 ;   in_taxon EFO:NCBITaxon:9606
Definition Sources: NCIT:C3507

paths to the root