Disease ID | Source | Name | Description |
614809 | OMIM | CFHR5 deficiency (CFHR5D) | A progressive disease characterized by glomerulonephritis, hematuria, renal failure, end-stage renal disease, subendothelial and mesangial glomerular C3 deposits, mesangial matrix expansion, increased glomerular cellularity, and segmental capillary wall thickening. Hematuria may become apparent after respiratory infections. The disease is caused by variants affecting the gene represented in this entry. |