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Ontology Browser

Term:
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 +   
A glomerulonephritis characterized by build up of IgA antibody in the glomerulus. (DO)
IgG4-related disease  
IMMUNE DYSREGULATION, AUTOIMMUNITY, AND AUTOINFLAMMATION  
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  
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 +   
Spondyloenchondrodysplasia  
subacute glomerulonephritis 
VEXAS syndrome  
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia  

Synonyms
Exact Synonyms: Berger disease ;   Berger's IgA or IgG nephropathy ;   Berger's disease ;   Bergers Disease ;   Glomerulonephritides, IGA ;   IGA Nephropathy ;   IGA Type Nephritis ;   IGAN ;   IGAN1 ;   IGAN2 ;   IGAN3 ;   IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1 ;   IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2 ;   Iga Nephropathy 1 ;   focal glomerulonephritis ;   immunoglobulin A nephropathy ;   primary IgA nephropathy ;   segmental glomerulonephritis ;   susceptibility to IgA nephropathy-3
Related Synonyms: Iga nephropathy, susceptibility to ;   susceptibility to progression to renal failure in IgA nephropathy
Primary IDs: MESH:D005922
Alternate IDs: OMIM:161950 ;   OMIM:613944 ;   OMIM:616818
Xrefs: EFO:0004194 ;   GARD:863 ;   NCI:C34643 ;   NCI:C35280 ;   OMIM:PS161950
Definition Sources: http://en.wikipedia.org/wiki/IgA_nephropathy "DO" "DO", http://www.nlm.nih.gov/medlineplus/ency/article/000466.htm "DO" "DO"

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