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Ontology Browser

Parent Terms Term With Siblings Child Terms
autoimmune disease +     
glomerulonephritis +     
Acquired Pulmonary Alveolar Proteinosis  
acute poststreptococcal glomerulonephritis 
acute proliferative glomerulonephritis +   
Addison's disease +   
Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity  
anti-basement membrane glomerulonephritis  
Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis +   
antisynthetase syndrome  
autoimmune disease of blood +   
autoimmune disease of cardiovascular system +   
autoimmune disease of endocrine system +   
autoimmune disease of exocrine system +   
autoimmune disease of gastrointestinal tract +   
autoimmune disease of musculoskeletal system +   
autoimmune disease of the nervous system +   
autoimmune disease of urogenital tract +   
Autoimmune Hypophysitis 
autoimmune interstitial lung, joint, and kidney disease  
autoimmune lymphoproliferative syndrome +   
Autoimmune Progesterone Dermatitis 
C1q Deficiency +   
chronic rapidly progressive glomerulonephritis 
CINCA syndrome  
Combined Immunodeficiency with Autoimmunity and Spondylometaphyseal Dysplasia  
common variable immunodeficiency +   
Diabetes Mellitus, Congenital Autoimmune  
diffuse glomerulonephritis +  
Experimental Autoimmune Uveitis +   
exudative glomerulonephritis 
familial mediterranean fever +   
focal embolic glomerulonephritis 
Gardner-Diamond Syndrome 
glomerulosclerosis +   
IgA glomerulonephritis +   
IgG4-related disease  
immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome  
immune-complex glomerulonephritis  
Immunodeficiency 113  
Immunodeficiency 78 with Autoimmunity and Developmental Delay  
Immunodeficiency 85  
Immunodeficiency 87 and Autoimmunity  
Immunodeficiency 89 and Autoimmunity  
Jaccoud's syndrome 
Linear IgA Bullous Dermatosis 
lipoid nephrosis  
lupus nephritis  
Lymphopenic Hypergammaglobulinemia, Antibody Deficiency, Autoimmune Hemolytic Anemia, and Glomerulonephritis 
Marfanoid Habitus with Microcephaly and Glomerulonephritis 
membranous glomerulonephritis  
A type of glomerulonephritis that is characterized by the accumulation of immune deposits (COMPLEMENT MEMBRANE ATTACK COMPLEX) on the outer aspect of the GLOMERULAR BASEMENT MEMBRANE. It progresses from subepithelial dense deposits, to basement membrane reaction and eventual thickening of the basement membrane.
mesangial proliferative glomerulonephritis +   
Multisystem Autoimmune Disease with Facial Dysmorphism  
Multisystem Autoimmune Disease, Infantile-Onset +   
Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal infections 
proliferative glomerulonephritis 
rapidly progressive glomerulonephritis +   
subacute glomerulonephritis 
VEXAS syndrome  
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia  

Exact Synonyms: CONGENITAL MEMBRANOUS NEPHROPATHY DUE TO FETOMATERNAL ANTI-NEUTRAL ENDOPEPTIDASE ALLOIMMUNIZATION ;   Extramembranous Glomerulopathy ;   Heymann Nephritis ;   Idiopathic Membranous Glomerulonephritis ;   Idiopathic Membranous Nephropathy ;   MBNP ;   Membranous Glomerulonephritides ;   Membranous Glomerulonephropathy ;   idiopathic membranous glomerulonephritides ;   membranous glomerulopathy ;   membranous nephropathy
Related Synonyms: membranous nephropathy, susceptibility to
Primary IDs: MESH:D015433
Alternate IDs: OMIM:614692
Xrefs: EFO:0004254 ;   ICD10CM:N03.2 ;   NCI:C34645
Definition Sources: MESH:D015433

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