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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Abnormal Neutrophil Chemotactic Response 
Autoimmune Diseases +   
Chondroitin-6-Sulfaturia, Defective Cellular Immunity, Nephrotic Syndrome 
fetal erythroblastosis +   
Graft vs Host Disease  
The clinical entity characterized by anorexia, diarrhea, loss of hair, leukopenia, thrombocytopenia, growth retardation, and eventual death brought about by the GRAFT VS HOST REACTION.
hypersensitivity reaction disease +   
IMAGEI Syndrome  
Immune Reconstitution Inflammatory Syndrome 
Immune Response to Synthetic Polypeptide--IrGAT 
Immune Suppression 
immune system cancer +   
Immunoproliferative Disorders +   
Immunoskeletal Dysplasia with Neurodevelopmental Abnormalities  
INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY  
lymphatic system disease +   
Lymphoblastic Transformation, Inhibition of 
membranoproliferative glomerulonephritis +   
Monocyte Chemotactic Disorder 
otulipenia  
primary immunodeficiency disease +   
Pseudo-TORCH Syndrome 2  
Pseudo-TORCH Syndrome 3  
Radiation Sensitivity of Natural Killer Activity 
Thrombocytopenic Purpura +   
Transfusion Reaction 
Transplant Rejection +   

Synonyms
Exact Synonyms: GRAFT-VERSUS-HOST DISEASE, SUSCEPTIBILITY TO ;   GVHD ;   GVHDS ;   Graft Versus Host Disease ;   Graft-Versus-Host Diseases ;   Graft-vs-Host Diseases ;   Homologous Wasting Disease ;   Runt Disease
Related Synonyms: GRAFT-VERSUS-HOST DISEASE, RESISTANCE TO ;   PLATELET-ENDOTHELIAL CELL ADHESION MOLECULE 1 POLYMORPHISM
Primary IDs: MESH:D006086 ;   RDO:0005695
Alternate IDs: OMIM:614395
Definition Sources: MESH:D006086

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