Familial idiopathic steroid-resistant nephrotic syndrome is characterized by a nephrotic syndrome with often early onset.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation | MONDO:0019652 | ||
| Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis | MONDO:0019654 | ||
| Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes | MONDO:0019653 | ||
| Familial steroid-resistant nephrotic syndrome with sensorineural deafness | MONDO:0013836 | COQ6 | |
| Focal segmental glomerulosclerosis 1 | MONDO:0011303 | ACTN4 | |
| Nephrotic syndrome, type 10 | MONDO:0014373 | EMP2 | |
| Nephrotic syndrome, type 11 | MONDO:0014752 | NUP107 | |
| Nephrotic syndrome, type 12 | MONDO:0014817 | NUP93 | |
| Nephrotic syndrome, type 13 | MONDO:0014818 | NUP205 | |
| Nephrotic syndrome, type 2 | MONDO:0010974 | NPHS2 | |
| Nephrotic syndrome, type 3 | MONDO:0012546 | PLCE1 | |
| Nephrotic syndrome, type 6 | MONDO:0013619 | PTPRO | |
| Nephrotic syndrome, type 8 | MONDO:0014099 | ARHGDIA | |
| Nephrotic syndrome, type 9 | MONDO:0014257 | COQ8B |
Rare disease
Including projects on subtypes.
No projects yet.