Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Ontology Browser

membranoproliferative glomerulonephritis (DOID:2920)
Annotations: Rat: (39) Mouse: (38) Human: (38) Chinchilla: (35) Bonobo: (37) Dog: (37) Squirrel: (32) Pig: (35)
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  
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  
lymphatic system disease +   
Lymphoblastic Transformation, Inhibition of 
membranoproliferative glomerulonephritis +   
Chronic glomerulonephritis characterized histologically by proliferation of MESANGIAL CELLS, increase in the MESANGIAL EXTRACELLULAR MATRIX, and a thickening of the glomerular capillary walls. This may appear as a primary disorder or secondary to other diseases including infections and autoimmune disease SYSTEMIC LUPUS ERYTHEMATOSUS. Various subtypes are classified by their abnormal ultrastructures and immune deposits. Hypocomplementemia is a characteristic feature of all types of MPGN.
Monocyte Chemotactic Disorder 
primary immunodeficiency disease +   
Pseudo-TORCH Syndrome 2  
Pseudo-TORCH Syndrome 3  
Radiation Sensitivity of Natural Killer Activity 
Thrombocytopenic Purpura +   
Transfusion Reaction 
Transplant Rejection +   

Exact Synonyms: Dense Deposit Disease ;   Hypocomplementemic Glomerulonephritides ;   Hypocomplementemic Glomerulonephritis ;   Lobular glomerulonephritis ;   MPGN ;   Membranoproliferative Glomerulonephritides ;   Membranoproliferative Glomerulonephritis, Type I ;   Mesangiocapillary Glomerulonephritides ;   Mesangiocapillary Glomerulonephritis ;   Mesangiocapillary Glomerulonephritis, Type I ;   Subendothelial Membranoproliferative Glomerulonephritis ;   chronic glomerulonephritis, lobular
Narrow Synonyms: MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS WITH COMPLEMENT FACTOR H DEFICIENCY ;   MESANGIOCAPILLARY GLOMERULONEPHRITIS, TYPE II ;   Membranoproliferative Glomerulonephritis Type II ;   Membranoproliferative Glomerulonephritis, Type III
Primary IDs: MESH:D015432
Alternate IDs: RDO:0002519
Xrefs: GARD:11982 ;   NCI:C34644 ;   OMIM:PS137950
Definition Sources: MESH:D015432

paths to the root


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