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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