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IgA nephropathy, susceptibility to, 3
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any IgA glomerulonephritis in which the cause of the disease is a mutation in the SPRY2 gene.
Uniprot Description A form of IgA nephropathy, a common primary glomerulonephritis characterized by glomerular sclerosis, interstitial fibrosis, and mesangial glomerular deposits of immunoglobulin A and immunoglobulin G visible on renal biopsies. IgA nephropathy is associated with renal insufficiency that can progress to end-stage renal disease. Proteinuria and hematuria are characteristic clinical presentations.
Mondo Term and Equivalent IDs
MONDO:0014786: IgA nephropathy, susceptibility to, 3
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
OMIM:616818
MONDO:0014786
High level summary of knowledge for a disease, including descriptions and datasource references.