An instance of nephrotic syndrome that is caused by an inherited modification of the individual's genome.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Familial idiopathic steroid-resistant nephrotic syndrome | MONDO:0019006 | 14 | |
| LAMB2-related infantile-onset nephrotic syndrome | MONDO:0013621 | 1 | LAMB2 |
| Congenital nephrotic syndrome, Finnish type | MONDO:0009732 | NPHS1 | |
| Idiopathic multidrug-resistant nephrotic syndrome | MONDO:0035459 | DAAM2 | |
| Immunoglobulin-mediated membranoproliferative glomerulonephritis | MONDO:0014005 | DGKE | |
| Nephrotic syndrome 14 | MONDO:0033203 | SGPL1 | |
| Nephrotic syndrome 15 | MONDO:0033262 | MAGI2 | |
| Nephrotic syndrome 16 | MONDO:0033280 | KANK2 | |
| Nephrotic syndrome, IIa 26 | MONDO:0031061 | LAMA5 | |
| Nephrotic syndrome, type 17 | MONDO:0032580 | NUP85 | |
| Nephrotic syndrome, type 18 | MONDO:0032581 | NUP133 | |
| Nephrotic syndrome, type 19 | MONDO:0032582 | ||
| Nephrotic syndrome, type 20 | MONDO:0026726 | TBC1D8B | |
| Nephrotic syndrome, type 21 | MONDO:0032826 | AVIL | |
| Nephrotic syndrome, type 22 | MONDO:0030895 | NOS1AP | |
| Nephrotic syndrome, type 23 | MONDO:0030962 | KIRREL1 | |
| Nephrotic syndrome, type 24 | MONDO:0031008 | DAAM2 | |
| Nephrotic syndrome, type 4 | MONDO:0009733 | WT1 |
Including projects on subtypes.
No projects yet.